Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Poonam Verma Shivkumar"'
Autor:
Asoke K Pal, Prafulla S Ambulkar, Jwalant E Waghmare, Moreshwar R Shende, Manish Jain, Poonam Verma Shivkumar
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 5, Pp GC01-GC06 (2020)
Introduction: The chromosomal anomalies are the most significant cause of human genetic disorders. Various types of structural and numerical chromosome aberrations have been identified in clinically suspect of genetic disorders. These aberrations are
Externí odkaz:
https://doaj.org/article/48b963456d4f40f48d918bcd05dfe7b7
Autor:
Prafulla S. Ambulkar, Jwalant E. Waghmare, Poonam Verma Shivkumar, Ajay R. Chaudhari, Nitin M. Gangane, Pratibha Narang, Asoke K. Pal
Publikováno v:
AndrologiaREFERENCES. 54(11)
Spermatogenesis is regulated by complex tissue specific gene expression in the testis to achieve normal male fertility. X-chromosome specific TATA binding protein (TBP)-associated factor 7L (hTAF7L) is one of the transcriptional regulator genes consi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f041f577d62a98ba19e6b64a6449f6
https://pubmed.ncbi.nlm.nih.gov/36068176
https://pubmed.ncbi.nlm.nih.gov/36068176
Autor:
Pratibha Narang, Poonam Verma Shivkumar, Asoke K Pal, Jwalant E Waghmare, Prafulla S. Ambulkar
Publikováno v:
Andrologia. 53
The SRY initiates cascade of gene expression that transforms the undifferentiated gonad, genital ridge into testis. Mutations of the SRY gene is associated with complete gonadal dysgenesis in females with 46,XY karyotype. Primary amenorrhea is one of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b89ed2eecc021a88e2e5592974945363
https://doi.org/10.1111/and.14011
https://doi.org/10.1111/and.14011
Autor:
Prafulla S. Ambulkar, Poonam Verma Shivkumar, Asoke K Pal, Manish Jain, M.R. Shende, Jwalant E Waghmare
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 5, Pp GC01-GC06 (2020)
Introduction: The chromosomal anomalies are the most significant cause of human genetic disorders. Various types of structural and numerical chromosome aberrations have been identified in clinically suspect of genetic disorders. These aberrations are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::736fc72baa1cf18cd25360b60ab0fe7f
https://doi.org/10.7860/jcdr/2020/43678.13688
https://doi.org/10.7860/jcdr/2020/43678.13688
Autor:
Pankhuri Sharma, Jagannath Behera, Archana Sarkar, Sunil Mehra, Poonam Verma Shivkumar, Simi Khan
Publikováno v:
HIV: Current Research.
Objectives: The importance of knowing HIV status is a key strategy for HIV response and effective treatment services. The present study aimed to assess feasibility of using oral- fluid based rapid HIV test aided by FrontlineHealth workers (FLWs) of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cd36bda504c5dd6d51483201ebb37f1
https://doi.org/10.4172/2572-0805.1000127
https://doi.org/10.4172/2572-0805.1000127