المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., orcid:0000-0002-9802-0880, Temel, Şehime, AAG-8385-2021, 6507885442

مصطلحات موضوعية: Variants, Azoospermia, Genetics & heredity, Adult, Alleles, Animals, Cell cycle checkpoints, Homozygote, Humans, Infertility, male, Meiosis, Mice, Mutation, Phenotype, Proteins, Spermatogenesis, Spermatozoa, Testis, Turkey, Whole exome sequencing, Male Infertility, Y Chromosome, Meiosis 1 arresting protein, mouse, Protein, Allele, Article, Cryptozoospermia, Disease severity

وصف الملف: application/pdf

العلاقة: Makale - Uluslararası Hakemli Dergi; KUAP(T)-2014/36; American Journal of Human Genetics; Yurt içi; Yurt dışı; Sanayi; Wyrwoll, M. J. vd. (2020). "Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility". American Journal of Human Genetics, 107(2), 342-351.; https://doi.org/10.1016/j.ajhg.2020.06.010Test; https://www.sciencedirect.com/science/article/pii/S0002929720301981Test; http://hdl.handle.net/11452/30096Test; 000558491800014; 2-s2.0-85088861386; 341; 351; 107

الإتاحة: https://doi.org/10.1016/j.ajhg.2020.06.010Test
http://hdl.handle.net/11452/30096Test
https://www.sciencedirect.com/science/article/pii/S0002929720301981Test

المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., orcid:0000-0002-9802-0880, Temel, Şehime, AAG-8385-2021, 6507885442

مصطلحات موضوعية: Variants, Azoospermia, Genetics & heredity, Adult, Alleles, Animals, Cell cycle checkpoints, Homozygote, Humans, Infertility, male, Meiosis, Mice, Mutation, Phenotype, Proteins, Spermatogenesis, Spermatozoa, Testis, Turkey, Whole exome sequencing, Male Infertility, Y Chromosome, Meiosis 1 arresting protein, mouse, Protein, Allele, Article, Cryptozoospermia, Disease severity

وصف الملف: application/pdf

العلاقة: Makale - Uluslararası Hakemli Dergi; KUAP(T)-2014/36; American Journal of Human Genetics; Yurt içi; Yurt dışı; Sanayi; Wyrwoll, M. J. vd. (2020). "Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility". American Journal of Human Genetics, 107(2), 342-351.; https://doi.org/10.1016/j.ajhg.2020.06.010Test; https://www.sciencedirect.com/science/article/pii/S0002929720301981Test; http://hdl.handle.net/11452/30096Test; 000558491800014; 2-s2.0-85088861386; 341; 351; 107

الإتاحة: https://doi.org/10.1016/j.ajhg.2020.06.010Test
http://hdl.handle.net/11452/30096Test
https://www.sciencedirect.com/science/article/pii/S0002929720301981Test

المؤلفون: Gül, Cuma Bülent

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Endokrinoloji ve Metabolizma Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı., orcid:0000-0001-7625-9148, orcid:0000-0003-0463-6818, Gül, Özen Öz, Cander, Soner, Budak, Ferah, Oral, Barbaros, Ersoy, Canan, AAI-1005-2021, F-4657-2014, K-7285-2012, AAH-8861-2021, 26040787100, 25027068600, 6701913697, 7004498001, 6701485882

مصطلحات موضوعية: Obstetrics & gynecology, Polycystic ovary syndrome, Cytokine signalling, SOCS1 polymorphism, Insulin resistance, Women, Prevalence, Expression, Variants, Proteins, Glucose, Obesity, Health, Adult, Body mass index, Case-control studie, Cholesterol, LDL, Female, Gene frequency, Humans, Logistic models, Middle aged, Polymerase chain reaction, Polymorphism, Genetic, Premenopause, Suppressor of cytokine signaling 1 protein, Triglycerides, Turkey

العلاقة: Makale - Uluslararası Hakemli Dergi; Journal of Obstetrics and Gynaecology; Sanayi; Gül, Ö. Ö. vd. (2017). ''Cytokine signal suppressor (SOCS) 1-1478 CA/del gene polymorphism in Turkish patients with polycystic ovary syndrome''. Journal of Obstetrics and Gynaecology, 37(7), 896-901.; https://doi.org/10.1080/01443615.2017.1309011Test; http://hdl.handle.net/11452/31884Test; 000411307000012; 2-s2.0-85020197942; 896; 901; 37

الإتاحة: https://doi.org/10.1080/01443615.2017.1309011Test
http://hdl.handle.net/11452/31884Test