Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Asoke K Pal"'
Autor:
Asoke K Pal, Prafulla S Ambulkar, Bharat R Sontakke, Shweta S Talhar, Pradeep Bokariya, Vijay K Gujar
Publikováno v:
Journal of Human Reproductive Sciences, Vol 12, Iss 1, Pp 29-34 (2019)
Background: Primary amenorrhea is one of the most common disorders seen as gynecological problems in adolescent girls. It refers to the participants who did not attain menarche by the age of 11–15 years. Chromosome abnormalities contribute as one o
Externí odkaz:
https://doaj.org/article/10230df37440473aa5b9b9ddc63890fc
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 Human Reproductive Sciences, Vol 9, Iss 1, Pp 35-40 (2016)
OBJECTIVE: To determine the association of large-scale mitochondrial DNA (mtDNA) deletions with abnormal sperm or abnormal flagellar movement of human spermatozoa in asthenozoospermia and oligoasthenoteratozoospermia (OAT) subjects using percoll grad
Externí odkaz:
https://doaj.org/article/5cec2334c06f48679fe3bd00bcc33ca7
Autor:
PRAFULLA S. AMBULKAR, RAMJI SIGH, MVR REDDY, POONAM S. VARMA, DILIP O. GUPTA, MORESHWAR R SHENDE, ASOKE K PAL
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 3, Pp 88-91 (2014)
Background: Genetic factors cause about 15% of male infertility. Azoospermia factors (AZFa, AZFb, and AZFc) present on Yq are most important for spermatogenesis. We have made an attempt to evaluate the frequencies of microdeletions of AZFa, AZFb,
Externí odkaz:
https://doaj.org/article/ffe37a8bbd7245b59b1aa91d0dc35e1f
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
Autor:
Pratibha Narang, Asoke K Pal, M.R. Shende, Pranita Waghmare, Bharat R Sontakke, Shweta S Talhar, Prafulla S. Ambulkar
Publikováno v:
Indian Journal of Tuberculosis. 66:227-233
Pulmonary tuberculosis (PTB) remains a major cause of morbidity and mortality all around the world. Recent studies have pointed out increased oxidative stress and also DNA damage in peripheral blood in PTB. Till date, to the best of our knowledge, no
Autor:
Bharat R Sontakke, Prafulla S. Ambulkar, M S Bharambe, Shweta S Talhar, Poonam V Shivkumar, Asoke K Pal
Publikováno v:
Journal of Cytology, Vol 36, Iss 1, Pp 32-37 (2019)
Journal of Cytology
Journal of Cytology
Background: Carcinoma cervix of uterus (CaCx) is the most common malignancy affecting women worldwide. It is an established fact that infection of specific types of human papilloma virus (HPV) is essential for the development of cervical cancer. The
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
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