Zobrazeno 1 - 10
of 14 020
pro vyhledávání: '"homozygosity mapping"'
Autor:
Perfilyeva, Anastassiya1 (AUTHOR), Bespalova, Kira1,2 (AUTHOR) kira.b.bespalova@gmail.com, Bespalov, Sergey3 (AUTHOR), Begmanova, Mamura1 (AUTHOR), Kuzovleva, Yelena1 (AUTHOR), Vishnyakova, Olga4 (AUTHOR), Nazarenko, Inna5 (AUTHOR), Abylkassymova, Gulnar1 (AUTHOR), Perfilyeva, Yuliya6 (AUTHOR), Plakhov, Konstantin7 (AUTHOR), Djansugurova, Leyla1 (AUTHOR), Bekmanov, Bakhytzhan1,2 (AUTHOR)
Publikováno v:
Scientific Reports. 7/3/2023, Vol. 13 Issue 1, p1-10. 10p.
Autor:
Anastassiya Perfilyeva, Kira Bespalova, Sergey Bespalov, Mamura Begmanova, Yelena Kuzovleva, Olga Vishnyakova, Inna Nazarenko, Gulnar Abylkassymova, Yuliya Perfilyeva, Konstantin Plakhov, Leyla Djansugurova, Bakhytzhan Bekmanov
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract The Tazy is a breed of sighthound common in Kazakhstan. The identification of runs of homozygosity (ROH) is an informative approach to assessing the history and possible patterns of directional selection pressure. To our knowledge, the prese
Externí odkaz:
https://doaj.org/article/7b0188ed9480419db71d56c904d092cb
Akademický článek
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Publikováno v:
The Plant Genome, Vol 16, Iss 2, Pp n/a-n/a (2023)
Abstract Homozygosity mapping is an effective tool for detecting genomic regions responsible for a given trait when the phenotype is controlled by a limited number of dominant or co‐dominant loci. Freezing tolerance is a major attribute in agricult
Externí odkaz:
https://doaj.org/article/4952aa5aa8e34c86abe578a2b22fc441
Autor:
Jiao, Bin, Zhou, Zhifan, Hu, Zhengmao, Du, Juan, Liao, Xinxin, Luo, Yingying, Wang, Junling, Yan, Xinxiang, Jiang, Hong, Tang, Beisha, Shen, Lu
Publikováno v:
In Parkinsonism and Related Disorders November 2020 80:65-72
Autor:
Sherif, Maha1, Demirbilek, Hüseyin1,2,3 dr_huseyin@hotmail.com, Çayır, Atilla4, Tahir, Sophia1, Çavdarlı, Büşra5, Demiral, Meliha6, Cebeci, Ayşe Nurcan7, Vurallı, Doğuş3, Rahman, Sofia Asim1, Unal, Edip6, Büyükyılmaz, Gönül8, Baran, Rıza Taner2, Özbek, Mehmet Nuri2,6, Hussain, Khalid1,9
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. Mar2021, Vol. 13 Issue 1, p34-43. 10p.
Publikováno v:
In Clinica Chimica Acta July 2019 494:64-70
Autor:
Alayoubi, Abdulfatah M.1 (AUTHOR), Alfadhli, Fatima2 (AUTHOR), Mehnaz3 (AUTHOR), Albalawi, Alia M.4 (AUTHOR), Ramzan, Khushnooda5 (AUTHOR), Jelani, Musharraf3 (AUTHOR), Basit, Sulman1,4,6 (AUTHOR) sbasit.phd@gmail.com
Publikováno v:
Scientific Reports. 10/25/2024, Vol. 14 Issue 1, p1-9. 9p.
Autor:
Maha Sherif, Hüseyin Demirbilek, Atilla Çayır, Sophia Tahir, Büşra Çavdarlı, Meliha Demiral, Ayşe Nurcan Cebeci, Doğuş Vurallı, Sofia Asim Rahman, Edip Unal, Gönül Büyükyılmaz, Riza Taner Baran, Mehmet Nuri Özbek, Khalid Hussain
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 34-43 (2021)
Objective:Bi-allelic mutations in the wolframin gene (WFS1) cause Wolfram syndrome 1 (WS1 or DIDMOAD) characterized by non-autoimmune diabetes mellitus, optic atrophy, diabetes insipidus, sensorineural deafness, urinary tract abnormalities, and neuro
Externí odkaz:
https://doaj.org/article/98ad2c4ca25547f1b7b9db3e4bc101ad
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Recent studies of the genetic foundations of cognitive ability rely on large samples (in extreme, hundreds of thousands) of individuals from relatively outbred populations of mostly European ancestry. Hypothesizing that the genetic foundation of cogn
Externí odkaz:
https://doaj.org/article/e11f099f920d45cbbf9dd5c7d901ae88