Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Jwalant E Waghmare"'
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:
Asoke K Pal, Prafulla S Ambulkar, Jwalant E Waghmare, Vandana Wankhede, Moreshwar R Shende, Aaditya M Tarnekar
Publikováno v:
Journal of Human Reproductive Sciences, Vol 11, Iss 3, Pp 247-253 (2018)
Background: Recurrent pregnancy loss is a challenging reproductive problem, and chromosomal anomalies approximately affect 2%–8% of couples with recurrent pregnancy loss. The chromosomal abnormality, especially balanced translocation rearrangement
Externí odkaz:
https://doaj.org/article/8376edf5455445e9b0f8f8b7c915a9f4
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 5, Pp AC01-AC05 (2018)
Introduction: Variety of clinical disorders such as diabetes mellitus, chronic hypertension, renal artery stenosis, chronic renal failure affects the kidney and alters renal length. It also varies according to height, weight, age and ethnicity. So th
Externí odkaz:
https://doaj.org/article/1e2c762dbcff4a2cb40f16cc0c646703
Autor:
Shweta Sudhakar Talhar, Jwalant E Waghmare, Lipika Paul, Sushilkumar Kale, Moreshwar R Shende
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 6, Pp AC04-AC08 (2017)
Introduction: Knowledge of normal range of size and volume of abdominal organs plays a vital role in clinical practices as various medical conditions affects the abdominal organs causing alteration in their dimensions. Aim: The present retrospect
Externí odkaz:
https://doaj.org/article/ac1f2203e72246cf90835ac774569657
Publikováno v:
Journal of Mahatma Gandhi Institute of Medical Sciences, Vol 19, Iss 2, Pp 148-150 (2014)
The aim of this study was to report a congenital anomaly in a cadaveric dissection. During routine undergraduate dissection in a middle-aged male cadaver, we found that on the left side, there was a presence of an incompletely duplicated ureter. On t
Externí odkaz:
https://doaj.org/article/f39b12d4a73045bbb72f9d3b569e6779
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:
Vandana R Wankhede, M.R. Shende, Asoke K Pal, Prafulla S. Ambulkar, Jwalant E Waghmare, Aaditya Tarnekar
Publikováno v:
Journal of Human Reproductive Sciences, Vol 11, Iss 3, Pp 247-253 (2018)
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences
Background: Recurrent pregnancy loss is a challenging reproductive problem, and chromosomal anomalies approximately affect 2%–8% of couples with recurrent pregnancy loss. The chromosomal abnormality, especially balanced translocation rearrangement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bf65a504284fe2f5b43cec70cddd9f6
http://www.jhrsonline.org/article.asp?issn=0974-1208
http://www.jhrsonline.org/article.asp?issn=0974-1208
Autor:
Aaditya Tarnekar, Prafulla S. Ambulkar, Bharat R Sontakke, Jwalant E Waghmare, Asoke K Pal, M.R. Shende
Publikováno v:
The Nucleus. 60:209-220
Infertility affects very high percentage (15%) of couples and nearly 50% of these are accountable to the male partners. Reproduction encompassed two important biological processes are successful gametogenesis and fertility. Mainly, male infertility i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae7c6adad94e00d5e3a91a4f6c8ed3fb
https://doi.org/10.1007/s13237-017-0209-4
https://doi.org/10.1007/s13237-017-0209-4