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Ardından DNA'nın yapısı, dört baz (adenin, timin, sitozin ve guanin) ve genetik kodun nasıl oluştuğu açıklanır. İnsan, şempanze, resus maymunu gibi farklı canlı türlerinin kromozom sayıları karşılaştırılır ve DNA'nın diğer canlı türleriyle paylaşımı hakkında bilgiler verilir. Video, insanların birbirlerinden farklı kılan faktörlerin bir sonraki videoda anlatılacağını belirterek sona erer."]},"endTime":207,"title":"Genetik Bilgiler ve DNA Yapısı","beginTime":0}],"fullResult":[{"index":0,"title":"Vücut ve Hücreler","list":{"type":"unordered","items":["Vücümuz elli trilyon hücreden oluşur ve bu hücreler farklı işlevlere sahiptir.","Neredeyse tüm hücrelerin ortak yönü çekirdek ve mitokondri içermeleridir.","Çekirdek genlerimizin %99,9'unu içerirken, mitokondride birkaç tane daha gen vardır."]},"beginTime":0,"endTime":26,"href":"/video/preview/12932260200185767628?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=0&ask_summarization=1"},{"index":1,"title":"Genler ve DNA","list":{"type":"unordered","items":["Bilinene göre neredeyse yirmi bin genimiz vardır ve genler deoksiribonükleik asit (DNA) molekülünün küçük parçalarıdır.","Tüm genlerinizi taşıyan DNA'ları yan yana sıraladığınızda 180 cm uzunluğunda olurlar.","DNA, şeker, fosfat ve dört farklı bazdan (adenin, timin, sitozin ve guanin) oluşan çift sarmallı bir moleküldür."]},"beginTime":26,"endTime":75,"href":"/video/preview/12932260200185767628?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=26&ask_summarization=1"},{"index":2,"title":"Genetik Kod ve Genlerin İşlevi","list":{"type":"unordered","items":["Dört bazın sayısı ve düzeni bir canlıyı şempanze, inek, muz veya insan yapar.","Genlerde bazı özel proteinleri üretmenin tarifleri vardır ve bu tarifler ebeveynlerden çocuklara aktarılır.","Genler bir hücreye nasıl işlev göreceğini ve hangi özellikleri açığa çıkarması gerektiğini söyler."]},"beginTime":75,"endTime":141,"href":"/video/preview/12932260200185767628?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=75&ask_summarization=1"},{"index":3,"title":"Kromozomlar","list":{"type":"unordered","items":["Genlerimizi taşıyan DNA'nın büyük molekülleri kromozom adı verilen parçalara bölünür.","Farklı canlı türleri farklı sayılarda kromozoma sahiptir: İnsanlar 46, şempanzeler 48, resus maymunları 42, inekler 60, tavuklar 78, sirkesinekler 8 ve muzlar 22 kromozomu vardır.","DNA'nın %93'ünü resus maymunuyla, %98,5'ini şempanzeyle ve %99,5'ini diğer insanlarla paylaşıyoruz."]},"beginTime":141,"endTime":201,"href":"/video/preview/12932260200185767628?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=141&ask_summarization=1"}],"linkTemplate":"/video/preview/12932260200185767628?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"Genetik 101: Gen Nedir? 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fazlası için: http://www.khanacademy.org.tr Matematikten sanat tarihine, ekonomiden fen bilimlerine, basit toplamadan diferansiyel denklemlere, ilkokul seviyesinden üniversite seviyesine...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/4325500/e94f0f22d0bf52a1d2b0f093e48a82e8/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/kjy5bQAAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"8","reqid":"1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=videoid:17044460119935823102","teaser":[{"list":{"type":"unordered","items":["Bu video, genetik ve kromozomlar hakkında bilgi veren eğitici bir içeriktir.","Video, genlerin ailemizden nasıl aktarıldığını açıklayarak başlar ve kromozomların yapısını anlatır. Erkeklerin X ve Y kromozomları, kadınların ise genellikle iki X kromozomu olduğu, cinsiyetin babadan alınan X veya Y kromozomuyla belirlendiği açıklanır. Ayrıca, genetik rekombinasyon, kromozomların bölünmesi, sperm ve yumurta hücrelerinin oluşumu ve döllenme süreci detaylı olarak anlatılır. Video, genetik soyağacı takibi konusunda da bilgiler sunarak, Y kromozomu ve mitokondriyal DNA'nın soy takibi için daha kolay kullanılabileceğini belirtir."]},"endTime":209,"title":"Genetik ve Kromozomlar Hakkında Eğitim Videosu","beginTime":0}],"fullResult":[{"index":0,"title":"Genetik Miras ve Kromozomlar","list":{"type":"unordered","items":["Genlerimiz ailelerimizden, onların ailelerinden ve öyle devam ederek gelir.","Her birimizde yirmiüç tane olmak üzere iki set kromozom bulunur; bir set anneden, diğer set ise babadan gelir.","Anneden ve babadan alınan kromozomlar birlikte eştürel kromozom çiftleri oluşturur."]},"beginTime":7,"endTime":43,"href":"/video/preview/17044460119935823102?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=7&ask_summarization=1"},{"index":1,"title":"Cinsiyet Kromozomları ve Hücre Bölmeleri","list":{"type":"unordered","items":["X ve Y kromozomları özel olup, erkeklerin hem X hem de Y kromozomu varken kadınların genellikle iki X kromozomu vardır.","Cinsiyetimizi belirleyen kromozomu babamızdan alırız.","Genellikle yetişkinlerde iki set kromozom bulunurken, sperm ve yumurta hücrelerinde yirmiüç kromozomluk tek bir set vardır."]},"beginTime":43,"endTime":81,"href":"/video/preview/17044460119935823102?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=43&ask_summarization=1"},{"index":2,"title":"Genetik Rekombinasyon","list":{"type":"unordered","items":["Vücudumuz sperm veya yumurta hücreleri üretirken, çift olan kromozomlar ayrılır ve her çiftin bir üyesi rastgele bir hücreye yerleşir.","Bu nedenle ana rahmine düştüğümüzde hem annemizin hem de babamızın genlerinin yarısını almış oluruz.","Eştürel çiftler ayrıldığında bazen çaprazlama geçiş yapar ve aralarında rastgele bir DNA alışverişi olur, buna genetik rekombinasyon denir."]},"beginTime":81,"endTime":147,"href":"/video/preview/17044460119935823102?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=81&ask_summarization=1"},{"index":3,"title":"Soy İzleme ve Döllenme","list":{"type":"unordered","items":["Genlerimiz rekombinasyon sırasında karıştığı için çocuklarımıza aktardığımız kromozomlar, ailemizden aldığımız kromozomlarla tam olarak aynı olmaz.","Y kromozomu genellikle babadan oğula hiç bozulmadan geçerken, mitokondrisindeki DNA da çocuğa yalnızca anneden aktarılır.","Döllenme sırasında birleşen sperm ve yumurta hücreleri, hem annemizden hem de babamızdan yirmiüç tane kromozom olarak iki setli tek bir hücre oluştururlar."]},"beginTime":147,"endTime":196,"href":"/video/preview/17044460119935823102?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=147&ask_summarization=1"}],"linkTemplate":"/video/preview/17044460119935823102?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"Genetik 101: Genlerimiz Nereden Geliyor? 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Video, genetik konularını anlamak ve sınavlara hazırlanmak isteyenler için kapsamlı bir kaynak niteliğindedir."]},"endTime":3642,"title":"Genetik Dersi: Kalıtım, Çaprazlamalar ve Olasılıklar","beginTime":0}],"fullResult":[{"index":0,"title":"Genetik Dersinin Devamı","list":{"type":"unordered","items":["Uzun bir aradan sonra genetik dersinin devamı olarak, vizeden sonra görülen konularda bilgi verilecek.","Ders, biyoloji protesi ve asturucu tarafından gerçekleştirilmekte ve kaynak olarak yardımcı doçent Dr. Tülay Aşkın Çelik ve Doçent Dr. Serdar Koca hocaların anlatımları kullanılmaktadır.","Vizeden sonraki konular daha zor olacak ve ökaryotlarda gen haritalaması anlatılacak."]},"beginTime":0,"endTime":39,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=0&ask_summarization=1"},{"index":1,"title":"Punnet Kare ve Test Çaprazlaması","list":{"type":"unordered","items":["Punnet karesi, dişi-erkek çaprazlamasını belli bir kare içinde yaparak monohibrit çaprazlamalarda kolaylık sağlar.","Test çaprazlamasının amacı, homozigot ve heterozigot bireyleri ayırt etmektir.","Test çaprazlamasında, homozigot veya heterozigot bireyler küçük çekinik allele'li bireylerle çaprazlanır."]},"beginTime":39,"endTime":186,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=39&ask_summarization=1"},{"index":2,"title":"Genetik Hastalıklar ve Albinizm","list":{"type":"unordered","items":["Genetik hastalıkları taşıyıcı bir elenme sonucunda oluşan çocuklar %25'inde sağlıklı, %50'sinde taşıyıcı ve %25'sinde etkilenmiştir.","Albinizm, saçlar, kaşlar ve ten renginin beyazlaşması, vücuttaki tüylerin beyaz olması ve çekinik özellik göstermesi olan bir hastalıktır.","Heterozigot heterozigot çaprazlamada (%75) normal, (%25) albino çocuk oluşabilir."]},"beginTime":186,"endTime":299,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=186&ask_summarization=1"},{"index":3,"title":"Monohibrit ve Dihibrit Çaprazlamalar","list":{"type":"unordered","items":["Monohibrit, tek karakter içeren çaprazlamadır ve her mutant karakter hem dominant hem de çekinik formda bulunabilir.","Dihibrit çaprazlamada iki farklı karakter incelenir ve gamet oluşurken her bir karakterden birer allele alınır.","Dihibrit çaprazlamada 64 farklı gamet oluşabilirken, monohibrit çaprazlamada 16 farklı gamet oluşur."]},"beginTime":299,"endTime":438,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=299&ask_summarization=1"},{"index":4,"title":"Dallanma Yöntemi","list":{"type":"unordered","items":["Dallanma yöntemi, özellikle dihibrit çaprazlamalarda kullanılan ve karışık görünen ancak aslında kolay bir yöntemdir.","Dallanma yönteminde, genetik karakterlerin farklı kombinasyonları ağaç dalı gibi gösterilir."]},"beginTime":438,"endTime":476,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=438&ask_summarization=1"},{"index":5,"title":"Çapraz Çiftleşmeler ve Gametler","list":{"type":"unordered","items":["Çapraz çiftleşmelerde, DD BB GG gibi genotiplerden gametler elde edilir ve çaprazlama yöntemi kullanılır.","İki gametin birleşmesi sonucunda 8 tane gamet elde edilir, bu gametlerin birleşimiyle 64 tane farklı kombinasyon oluşur.","Punnet karesi monohibrit ve dihibrit kombinasyonlarında kullanılırken, trihibrit kombinasyonlarında hata oranının yüksek olduğu için kullanılmaz."]},"beginTime":479,"endTime":542,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=479&ask_summarization=1"},{"index":6,"title":"Çatal Dallandırma Yöntemi","list":{"type":"unordered","items":["Çatal dallandırma yönteminde, baştaki karakter her zaman yazılır ve baskın karakter üç çeyrek oranında homozigot veya heterozigot olarak bulunur.","Çekinik karakter bir çeyrek oranında bulunur ve çizgi kullanılarak belirtilir.","Her gen için üç çeyrek baskın, bir çeyrek çekinik oranında dallanma yapılır."]},"beginTime":542,"endTime":699,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=542&ask_summarization=1"},{"index":7,"title":"Sonuçların Hesaplanması","list":{"type":"unordered","items":["Çatal dallandırma yönteminde elde edilen sonuçlar çarpım ve toplama kuralı ile hesaplanır.","Örneğin, üç çeyrek oranının kendi içinde çarpılması 9/16 oranını verir.","Sonuçta 9/32 oranında DdBbGg kombinasyonu bulunur ve kare testine girecektir."]},"beginTime":699,"endTime":823,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=699&ask_summarization=1"},{"index":8,"title":"Çarpım Kuralı ve Döllenme Olasılıkları","list":{"type":"unordered","items":["Çarpım kuralı, gen tiplerinin döllenmeye katılma olasılıklarını hesaplamak için kullanılır.","Her gen tipinin döllenmeye katılma şansı yüzde elli'dir ve döllenmeye katılan birey tekrar katılamaz kuralı yoktur.","İki bağımsız olayın aynı anda olma olasılığı, ayrı ayrı olma olasılıklarının çarpımına eşittir."]},"beginTime":827,"endTime":880,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=827&ask_summarization=1"},{"index":9,"title":"Punnett Kareleri ve Çarpım İşlemi","list":{"type":"unordered","items":["Punnett karesi, gen tiplerinin kombinasyonlarını göstermek için kullanılan bir yöntemdir.","Çaprazlama işlemi yapılırken, her iki gen tipi birbirleriyle çarpılır ve olası kombinasyonlar bulunur.","Dallandırma yöntemi de kullanılabilir ancak Punnett karesi daha mantıklı ve karışıklığa neden olmaz."]},"beginTime":880,"endTime":998,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=880&ask_summarization=1"},{"index":10,"title":"Ki-Kare Testi","list":{"type":"unordered","items":["Ki-kare testi, gözlenen verilerin beklenen değerlerle uyumlu olup olmadığını test etmek için kullanılır.","Test formülü: (gözlenen - beklenen)² / beklenen şeklinde hesaplanır.","Ki-kare tablosunda serbestlik derecesi (n-1) ve istatistiksel anlamlılık düzeyi (genellikle 0.05) kullanılarak karşılaştırma yapılır."]},"beginTime":998,"endTime":1035,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=998&ask_summarization=1"},{"index":11,"title":"Ki-Kare Testi Örneği","list":{"type":"unordered","items":["Örnek olarak 1000 bezelyede iki öğrenci tarafından yapılan uzun ve kısa bezelye sayısı karşılaştırılır.","Çaprazlama yaparak gen tipleri belirlenir ve beklenen değerler hesaplanır.","Ki-kare değeri hesaplandıktan sonra, tablodaki değere karşılaştırılarak sonuçların doğruluğu değerlendirilir."]},"beginTime":1035,"endTime":1274,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1035&ask_summarization=1"},{"index":12,"title":"Genetik Çaprazlama ve Oranlar","list":{"type":"unordered","items":["Genetik çaprazlamada, çaprazlama karesi veya dallanma yöntemi kullanılarak gametlerin oluşumu gösterilir.","Dihibrit çaprazlamada 9:3:3:1 oranı görülür ve bu oran genetik hesaplamalarında önemlidir.","Gözlenen ve beklenen sonuçlar karşılaştırılarak farkın karesi bölü beklenen değer hesaplanır ve serbestlik derecesi ile karşılaştırılır."]},"beginTime":1279,"endTime":1515,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1279&ask_summarization=1"},{"index":13,"title":"Eksik Baskınlık","list":{"type":"unordered","items":["Eksik baskınlık, beklenen dominan karakter yerine ortaya çıkan farklı bir karakter durumudur.","Kırmızı ve beyaz çiçeklerin çaprazlanması sonucunda pembe çiçek ortaya çıkabilir, bu eksik baskınlık örneğidir.","Eksik baskınlık sonucunda 1:2:1 oranında kırmızı, pembe ve beyaz çiçekler oluşur."]},"beginTime":1515,"endTime":1588,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1515&ask_summarization=1"},{"index":14,"title":"Cinsiyet ve Kan Grupları","list":{"type":"unordered","items":["Lozof veya bargöz, kırmızı gözü, kısmi dominansından kaynaklanan eksik baskınlıktır.","Kan gruplarında MN çaprazlaması, bazı az kullanılan kan gruplarında görülen bir durumdur.","A ve B kan grupları birbirine dominant olabilir ve heterozigot durumlarda heterozis olarak adlandırılır."]},"beginTime":1588,"endTime":1708,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1588&ask_summarization=1"},{"index":15,"title":"Homozigot ve Heterozigot Durumlar","list":{"type":"unordered","items":["Oya kucağı anemisi, heterozigot durumda sıtma parazitinden daha az etkilenen bir durumdur.","Homozigot durumda oya kucağı anemisi, sıtma parazitinden daha çabuk etkilenir.","Genetik çalışmalarda sadece iki ayrı allele olmayabilir, bir yüz allele olabilir ancak birey iki tanesine sahip olabilir."]},"beginTime":1708,"endTime":1764,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1708&ask_summarization=1"},{"index":16,"title":"Kan Grupları","list":{"type":"unordered","items":["Kan grupları önemli bir konudur ve sınavlarda çok yüksek ihtimalle çıkar.","A kan grubu A veya A0 şeklinde, B kan grubu B veya B0 şeklinde, AB kan grubu ise sadece AB olarak bulunabilir.","A kan grubu taşıyan bireylerde H+NA glukozamider, B kan grubu taşıyanlarda H+galaktozamider, AB kan grubu taşıyanlarda hem NA glukozamider hem de galaktozamider bulunur."]},"beginTime":1767,"endTime":1859,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1767&ask_summarization=1"},{"index":17,"title":"RH Faktörü ve Kan Uyuşmazlığı","list":{"type":"unordered","items":["RH faktörü artı veya eksi olabilir ve RH pozitif RH+ ile, RH negatif RH- ile gösterilir.","RH negatif anne ve RH pozitif baba durumunda, ilk doğumda fazla görünmezken ikinci doğumda RH faktörü ile sorun ortaya çıkar.","Anne ve baba RH pozitif ise çocuk pozitif olmak zorunda, anne ve baba RH negatif ise çocuk negatif olur."]},"beginTime":1859,"endTime":1953,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1859&ask_summarization=1"},{"index":18,"title":"Farelerde Akut Özellik","list":{"type":"unordered","items":["Farelerde \"kıçlı renk\" adı verilen bir özellik vardır ve sarı farelerde akut genin varlığı gözlenmiş.","Sarı ve sarı farelerin çaprazlamasında F1 ve F2 nesillerde sadece akut (A) ve sarı (a) kombinasyonları oluşur, sadece akut olanlar yaşayamaz.","Akut ve sarı farelerin çaprazlamasında 3/4 oranında akut, 1/4 oranında sarı farlar oluşur."]},"beginTime":1953,"endTime":2077,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=1953&ask_summarization=1"},{"index":19,"title":"Mutant Bilginin Özellikleri","list":{"type":"unordered","items":["Mutant bilginin iki farklı özelliği vardır: yaşam açısından genotipik olarak resesif, ancak fenotipte dominant özellik gösterir.","Albino taşıyıcılığı ve kan grubu (A, B, AB, 0) kombinasyonu çaprazlamasında 1/16 oranında albino AB kan grubu, 1/16 oranında albino A kan grubu, 1/16 oranında albino B kan grubu ve 1/16 oranında albino 0 kan grubu oluşur.","Albino geni siyah genine baskındır, yani beyaz siyah siyah temsil ederken albino temsil eder."]},"beginTime":2077,"endTime":2423,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=2077&ask_summarization=1"},{"index":20,"title":"Genetik Muhabbetler ve Oranlar","list":{"type":"unordered","items":["Genetik muhabbetlerde A ve B genleri için 9:3:3:1 oranında sonuçlar elde edilir.","Dominant epistatik muhabbetlerde, A ve B genleri birleştiğinde 9:3:4 oranında sonuçlar oluşur.","Tamamlayıcı muhabbetlerde 12:3:1 oranında sonuçlar görülür."]},"beginTime":2433,"endTime":2783,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=2433&ask_summarization=1"},{"index":21,"title":"Cinsiyete Bağlı Kalıtım","list":{"type":"unordered","items":["Cinsiyete bağlı kalıtımda, erkeklerde X kromozomu üzerindeki genler homozigot olarak görülürken, dişilerde heterozigot olabilir.","Kırmızı göz geni X kromozomunda bulunur ve erkeklerde daha belirgin görülür.","Renk körlüğü ve hemofili gibi hastalıklar X kromozomuna bağlı olduğu için erkeklerde daha fazla gözlenir."]},"beginTime":2783,"endTime":3012,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=2783&ask_summarization=1"},{"index":22,"title":"Renk Körlüğü ve Kalıtım","list":{"type":"unordered","items":["Dişinin renk körü olması için babanın mutlaka renk körü olması ve annenin ya renk körü ya da taşıyıcı olması gerekir.","Erkeklerde Y kromozomu taşıyamadığı için taşıyıcı durumu söz konusu değildir, ya normal ya da hasta olurlar.","Chris cross kalıtım, cinsiyete bağlı hastalıkların kalıtım modelidir ve sınavlarda çıkabilir."]},"beginTime":3012,"endTime":3085,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3012&ask_summarization=1"},{"index":23,"title":"Eşeğiyle Sınırlı Kalıtım","list":{"type":"unordered","items":["Eşeğiyle sınırlı kalıtım, eşi hormonlarının varlığı ve yokluğuyla ilişki gösteren karakterlere denir; insandaki sakal ve bey çıkması bu tür bir örnektir.","İkiz yavrular çift yumurta ikiz değilse farklı cinsiyet olabilir; farklı cinsiyette sahip gebelikte erkek gelişimi 7. haftada, dişi gelişimi ise 9. haftada başlar.","Baskılanarak doğan dişilerde veya erkeklerde damızlık olarak kullanılmaz, kısırlık fazla görülür."]},"beginTime":3086,"endTime":3157,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3086&ask_summarization=1"},{"index":24,"title":"Eşeğiyle Sınırlı Kalıtım Örnekleri","list":{"type":"unordered","items":["Tavuk tüylenmesi, genotipi HH olursa hem dişi hem erkeğde görülürken, Hh genotipinde ise dişide erkek tüylenmesi, erkekte ise dişi tüylenmesi görülür.","Prostat kanseri erkeklerde, göğüs bürmesi ise dişilerde görülen hormonlarla ilgili olaylardır.","Boynuzlu-boynuzsuz örneğinde, B geni erkeklerde boynuzlu, dişilerde ise boynuzsuz görünüm verir."]},"beginTime":3157,"endTime":3238,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3157&ask_summarization=1"},{"index":25,"title":"Bilge ve Etkinlik","list":{"type":"unordered","items":["Bilge, bir genin birden fazla etki etmesi özelliğidir; örneğin aynı oyak hücresi bu konuda bilge olabilir.","Penetransiyon, bilgenin perotipte kendini gösterme sıklığıdır; %70-80 dominant bireyden %70'ı PN, %30'u YB'ye çıkıyorsa, mutant göstermesi gerekir.","İnsanda altı parmaklılık etkinlik gösterse de, bazen sadece el ve ayakta görülebilir."]},"beginTime":3238,"endTime":3288,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3238&ask_summarization=1"},{"index":26,"title":"Penetransiyonu Etkileyen Koşullar","list":{"type":"unordered","items":["Penetransiyonu etkileyen koşullar arasında sıcaklık, ışık ve beslenme bulunur.","Sıcaklığa bağlı olarak, siyah kedilerde kuyruk uçları, burun ve kulakları ısınmak için siyah renklidir; Himalaya tavşanlarında da aynı durum vardır.","Sıcaklıkta tüyleri kazınıp siyah olan uçlar sarılıp kapatılınca yeni çıkan tüylerin beyaz renkte çıktığı görülür; bu duruma koşullu mutasyon veya sıcaklık duyarlı mutasyonlar denir."]},"beginTime":3288,"endTime":3380,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3288&ask_summarization=1"},{"index":27,"title":"Genetik Damgalama (Imprinting)","list":{"type":"unordered","items":["Genetik damgalama (imprinting), kromozomların farklı fonksiyon göstereceği ve hangi ebeveynden geldiğini belirleyeceğidir.","PWS'de (Prader-Willi Sendromu) normal kromozom anneden, normal kromozom babadan gelir; zihinsel gerilik ve kontrolsüz iştah sorunu vardır.","ASD'de (Angelman Sendromu) normal kromozom babadan, normal kromozom anneden gelir; zihinsel gerilik ve yüz ifadesinde sürekli gülümseme vardır."]},"beginTime":3380,"endTime":3465,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3380&ask_summarization=1"},{"index":28,"title":"Genetik Damgalama Örnekleri","list":{"type":"unordered","items":["15. kromozom desiyonları üzerindeki bölge aynıdır; IGF2 geninde mutasyon yoksa fare normal boylu, iki mutant alel taşıyan cüce şeklinde olur.","Farenin boyutu hangi ebeveynden geldiğine göre değişir; normal anne ve mutant baba durumunda fare cüce oluşur.","Sutton 1903'te kromozom teorisini bulmuş, Morgan 1914'te 4. kromozomu gözlemlemiş ve haritasını çıkarmıştır."]},"beginTime":3465,"endTime":3526,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3465&ask_summarization=1"},{"index":29,"title":"Bağlı Genler ve Crossing Over","list":{"type":"unordered","items":["Farklı kromozomun üzerindeki genler birbirinden bağımsız şekilde hareket ederken, aynı kromozom üzerindeki genler bağlı genler olarak hareket edebilir.","Genler birbirinden ayrılıyorsa crossing over vardır; genler yakın ve tam bağlı değilse daha az crossing over vardır.","Genler yakın ve tam bağlıysa daha az crossing over vardır; %10-30 crossing over görülürse genler birbirine uzaktır."]},"beginTime":3526,"endTime":3640,"href":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=3526&ask_summarization=1"}],"linkTemplate":"/video/preview/11457066394140708976?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=%%timestamp%%&ask_summarization=1"},"isAdultDoc":false,"relatedParams":{"text":"Genetik 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uzun zamandır diğer canlıların genetiği üzerinde çok önemli etkileri oldu ve olmaya da devam ediyor... Daha fazlası için: http://www.khanacademy.org.tr Matematikten sanat tarihine...","preview":{"posterSrc":"//avatars.mds.yandex.net/get-vthumb/2812855/6cdf80baff1ac8f2df6351a7be584a79/564x318_1","videoSrc":"https://video-preview.s3.yandex.net/qPEvAwAAAAA.mp4","videoType":"video/mp4"},"target":"_self","position":"19","reqid":"1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL","summary":{"isFull":true,"fullTextUrl":"/video/result?ask_summarization=1&numdoc=1&noreask=1&nomisspell=1&parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=videoid:3536512087420792317","teaser":[{"list":{"type":"unordered","items":["Bu video, genetik mühendisliği konusunu anlatan eğitici bir içeriktir. Konuşmacı, genetik mühendisliğinin tarihsel gelişimini ve günümüzdeki uygulamalarını açıklamaktadır.","Video, genetik mühendisliğinin son elli yılda hayatımıza girdiğini ancak insanlar binlerce yıldır organizmaların genetiği üzerinde müdahale ettiğini anlatarak başlıyor. Köpeklerin evcilleştirilmesi ve elmaların tatlılaştırılması gibi örnekler üzerinden yapay seçilimin nasıl yapıldığını açıklıyor. Ardından rekombinant DNA teknolojisi, genetiği değiştirilmiş gıdalar (GDO) ve bunların faydaları ile riskleri ele alınıyor. Son bölümde ise insan genomuna müdahale etmenin etik boyutları ve biyoetik konuları tartışılıyor."]},"endTime":521,"title":"Genetik Mühendisliği ve Biyoetik","beginTime":0}],"fullResult":[{"index":0,"title":"Genetik Mühendisliğin Tarihi","list":{"type":"unordered","items":["Genetik mühendisliği son elli yılda hayatımıza giren bir bilim dalıdır, ancak genlerin kalıtım mekanizması olduğunu 20. yüzyılın ortalarına gelene kadar bilmiyorduk.","1970'lere gelene kadar genlere doğrudan müdahale etmeye kalkışmadık, ancak insanların çeşitli organizmaların genetiği üzerinde uzun zamandır ciddi etkileri oldu."]},"beginTime":0,"endTime":35,"href":"/video/preview/3536512087420792317?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=0&ask_summarization=1"},{"index":1,"title":"Doğal Seçilim Örneği: Köpekler","list":{"type":"unordered","items":["Kurtların alt türlerinden olan köpekler, tilki ve çakallarla akraba olup, nesiller boyu insanlar tarafından çeşitli özellikleri dikkate alınarak ehlileştirildi.","Köpekler, sevimli, uysal veya zararlı hayvanları yakalayarak hayatımızı kolaylaştırdığı için vahşi doğadan koparıldılar.","Binlerce yıl devam eden bu insan müdahalesinin sonucu olarak DNA'lar çeşitlendi ve farklı köpek ırkları ortaya çıktı."]},"beginTime":35,"endTime":124,"href":"/video/preview/3536512087420792317?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=35&ask_summarization=1"},{"index":2,"title":"Doğal Seçilim Örneği: Bitkiler","list":{"type":"unordered","items":["Günümüzde manavlarda gördüğümüz kıpkırmızı ve tatlı elmalar, binlerce yıl önce hiç de bugünkü gibi tatlı değildi.","Atalarımız tabiatta rastladıkları elmaların en tatlılarını, en büyüklerini ve en sulularını seçip uygun şartlarda yetiştirmeye başladılar.","Yıllar geçtikçe daha iri ve tatlı elmalar elde edildi, küçük, tatsız, ekşi ya da sert elmalar ise bugünü göremediler."]},"beginTime":124,"endTime":196,"href":"/video/preview/3536512087420792317?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=124&ask_summarization=1"},{"index":3,"title":"Genetik Mühendisliğin Doğuşu","list":{"type":"unordered","items":["Son otuz-kırk yıldır rastladığımız organizmaların genetik yapıları laboratuvar şartlarında değiştirilerek elde edilen meyve ve sebzeler genetik mühendisliğinin sonucudur.","Eskiden bilinçli olmadan doğal ve uzun bir sürecin sonunda elde ettiğimiz seçilimi mühendislik ile planlamaya başladık.","Genetik mühendisliği sayesinde çok daha hassas ve doğrudan genetik modifikasyonlar yapabiliyoruz."]},"beginTime":196,"endTime":249,"href":"/video/preview/3536512087420792317?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=196&ask_summarization=1"},{"index":4,"title":"Rekombinant DNA Teknolojisi","list":{"type":"unordered","items":["Rekombinant DNA, bir organizmadan alınan genlerin başka bir organizmaya aktarılması ve yeni yapay bir genetik yapı oluşturulması anlamına gelir.","Farklı organizmalardan elde edilen genlerin amaca yönelik olarak diğer organizmalara yerleştirilmesi, bazen bambaşka türler arasında da yapılabiliyor.","Örneğin, bir bitkiye böcek DNA'sı nakledilerek daha dayanıklı hale getirilebilir."]},"beginTime":249,"endTime":325,"href":"/video/preview/3536512087420792317?parent-reqid=1769567703200909-993246556889906496-balancer-l7leveler-kubr-yp-vla-208-BAL&text=Genetik&t=249&ask_summarization=1"},{"index":5,"title":"Genetik Mühendisliğin Faydaları ve Tartışmaları","list":{"type":"unordered","items":["Rekombinant DNA ve genetiği değiştirilmiş organizmalar (GDO) bugün kimi çevrelerde ciddi bir tartışma konusu.","Bu teknolojiler sayesinde daha dayanıklı ürünler yetiştirilebiliyor ve tükettiğimiz besinler daha besleyici hale getirilebiliyor.","Kimilerine göre tüm bu genetik müdahalelerin uzun vadede ne gibi sonuçlar 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