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pro vyhledávání: '"Mili Nailwal"'
Autor:
Mili Nailwal, Jenabhai B Chauhan
Publikováno v:
Journal of Human Reproductive Sciences, Vol 10, Iss 4, Pp 256-260 (2017)
The azoospermia factor (AZF) region on the Y chromosome consists of genes required for spermatogenesis. Among the three subregions, the AZFc subregion located at the distal portion of AZF is the driver for genetic variation in Y chromosome. The candi
Externí odkaz:
https://doaj.org/article/ec95d371a18b48f6b3e11e254dbfcda6
Autor:
Mili Nailwal, Jenabhai B Chauhan
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 8, Pp GC01-GC06 (2017)
Introduction: Azoospermia Factor (AZF) microdeletions in Yq chromosome is one of the most frequent genetic cause associated with failure of spermatogenesis in males with infertility. Aim: To figure out the Yq chromosome microdeletions frequency
Externí odkaz:
https://doaj.org/article/1b9d28d85edd44108a728178e579f59c
Autor:
Jenabhai B. Chauhan, Mili Nailwal
Publikováno v:
Meta Gene. 14:119-123
Background Male infertility is rising worldwide due to multiple etiological factors. Among the various causes, genetic cause contributes in disruption of spermatogenesis, especially due to Y chromosome microdeletions in azoospermia factor (AZF) regio
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:
Jenabhai B. Chauhan, Mili Nailwal
Publikováno v:
Systems Biology in Reproductive Medicine. 63:248-258
In living systems the most frequent type of genetic mutation is the single nucleotide polymorphism (SNP). Non-synonymous SNPs (nsSNPs) or missense mutations arise in coding regions of a particular gene. nsSNPs result in a single amino acid substituti
Autor:
Jenabhai B. Chauhan, Mili Nailwal
Publikováno v:
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences, Vol 10, Iss 4, Pp 256-260 (2017)
Journal of Human Reproductive Sciences, Vol 10, Iss 4, Pp 256-260 (2017)
The azoospermia factor (AZF) region on the Y chromosome consists of genes required for spermatogenesis. Among the three subregions, the AZFc subregion located at the distal portion of AZF is the driver for genetic variation in Y chromosome. The candi
Autor:
Mili Nailwal, Jenabhai B. Chauhan
Publikováno v:
Interdisciplinary sciences, computational life sciences. 11(3)
DEAD-box helicase 3, Y-linked (DBY) is a candidate gene of the AZF region which is involved in spermatogenesis process. Mutations in the DBY gene may disrupt the spermatogenesis and lead to infertility in men. Identification of functionally neutral m