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pro vyhledávání: '"USP9Y"'
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Publikováno v:
Fiyz̤, Vol 22, Iss 2, Pp 120-127 (2018)
Background: The increasing use of nanoparticles has raised concerns about the risks of nanoparticle release to the environment, which has adverse effects on fertility. Disruption of the expression of the USP9Y (Ubiquitin Specific Protease 9 Y chromos
Externí odkaz:
https://doaj.org/article/7815ad5ae8944b9ab1665c791e867075
Autor:
Giulia Guerri, Sandro La Vignera, Rosita A. Condorelli, Matteo Bertelli, Aldo E. Calogero, Federica Barbagallo, Stefano Paolacci, Rossella Cannarella
Publikováno v:
Asian Journal of Andrology
Asian Journal of Andrology, Vol 23, Iss 1, Pp 24-29 (2021)
Asian Journal of Andrology, Vol 23, Iss 1, Pp 24-29 (2021)
A large proportion of patients with idiopathic spermatogenic failure (SPGF; oligozoospermia or nonobstructive azoospermia [NOA]) do not receive a diagnosis despite an extensive diagnostic workup. Recent evidence has shown that the etiology remains un
Publikováno v:
Endokrynologia Polska. 71:58-65
Introduction: The aim of the study was to reveal the mechanisms for the pathogenesis and progression of type 1 diabetes mellitus (T1DM). Material and methods: Two mRNA expression profiles and two miRNA expression profiles were downloaded from the Gen
Publikováno v:
Jentashapir Journal of Cellular and Molecular Biology. 12
Background: Male factor infertility that is the cause of about half of the infertility cases, may occur due to azoospermia. Because spermatogenesis defects may lead to non-obstructive azoospermia (NOA), investigating the factors involved in spermatog
Autor:
Jian-Lin Han, Z. X. Guanque, Xiaocheng Zhao, Sun Yonggang, Xiaoting Xia, Zhijie Ma, Chen Shengmei, Lulan Zeng, Chuzhao Lei, J. T. Xu, Y. L. Xie, Ruizhe Li, S. Y. Chao
Publikováno v:
Animal Genetics. 49:618-622
The aim of the present study was to perform a preliminary analysis of the characterization and diversity of Y-chromosome haplotypes/haplogroups in yak of Qinghai Province, China. A total of 322 male yaks from nine populations belonging to three offic
Autor:
Hassan Ansari, Hamid Gourabi, Mostafa Rezaei-Tavirani, Sara Pahlavan, Shahab Mirshahvaladi, Anna Meyfour, Ghasem Hosseini Salekdeh, Hossein Baharvand
Publikováno v:
Journal of Proteome Research. 16:4391-4402
Despite evidence for sex-specific cardiovascular physiology and pathophysiology, the biological basis for this dimorphism remains to be explored. Apart from hormonal factors, gender-related characteristics may reside in the function of sex chromosome
Autor:
Jenabhai B. Chauhan, Mili Nailwal
Publikováno v:
Meta Gene. 13:124-128
Yq microdeletion is one of the well-known genetic causes of infertility in males which results in spermatogenetic impairment. Among the three regions (AZFa, AZFb and AZFc), deletion in Azoospermia Factor a (AZFa) sub-region of the human Y-chromosome
Autor:
Jenabhai B. Chauhan, Mili Nailwal
Publikováno v:
Meta Gene. 12:13-17
An important candidate gene on Y-chromosome is the ubiquitin-specific Protease 9, Y chromosome ( USP9Y ). Its role postulated is in the regulation of protein turnover. Mutation in this gene could interfere in the regulation of spermatogenesis resulti
Autor:
Maria Lorena Cordero-Maldonado, Pierre Garcia, Sandra Köglsberger, Manuel Buttini, Julia Ilona Forster, Alexander D. Crawford, Enrico Glaab, Paul Antony
Publikováno v:
Data in Brief, Vol 25, Iss, Pp-(2019)
Data in Brief, 25(1), 104130. New York, NY: Elsevier (2019).
Data in Brief, 25(1), 104130. New York, NY: Elsevier (2019).
Ubiquitin specific peptidase 9 (USP9) is a deubiquitinase encoded by a sex-linked gene with a Y-chromosomal form (USP9Y) and an X-chromosomal form (USP9X) that escapes X-inactivation. Since USP9 is a key regulatory gene with sex-linked expression in