Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kadupu Pavani"'
Autor:
Mamta Deendayal, Singh Rajender, Gyaneshwer Chaubey, Deepa Selvi Rani, Avinash A. Rasalkar, Kumarasamy Thangaraj, Baidyanath Chakravarty, Kadupu Pavani, Nalini J. Gupta
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Scientific Reports
Scientific Reports
Deletions in the AZoospermia Factor (AZF) regions (spermatogenesis loci) on the human Y chromosome are reported as one of the most common causes of severe testiculopathy and spermatogenic defects leading to male infertility, yet not much data is avai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab8dcde0fcf6b722cbfe25ffdaa0293d
https://doi.org/10.1038/s41598-019-42690-0
https://doi.org/10.1038/s41598-019-42690-0
Autor:
Mamata Deenadayal, Sisinthy Shivaji, Archana B. Siva, Nandini Rangaraj, Kadupu Pavani, Vaibhav Singh, Duvvuri Butchi Kameshwari, Curam Sreenivasacharlu Sundaram
Publikováno v:
MHR: Basic science of reproductive medicine. 16:452-462
With a view to understand the molecular basis of sperm motility, we have tried to establish the human sperm proteome by two-dimensional PAGE MALDI MS/MS analysis. We report identification of 75 different proteins in the human spermatozoa. Comparative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ebcbbe9ac1fa1e346b27d33c6ebbb1
https://doi.org/10.1093/molehr/gaq009
https://doi.org/10.1093/molehr/gaq009
Autor:
Bibaswan Ghosh, Lalji Singh, Kumarasamy Thangaraj, Deepa Selvi Rani, Alla G. Reddy, Subbaya Subramainan, Baidyanath Chakravarty, Nalini J. Gupta, Kadupu Pavani
Publikováno v:
Scopus-Elsevier
Genetic factors cause about 10% of male infertility. Azoospermia factors (AZFa, AZFb, AZFc) are considered to be the most important for spermatogenesis. We therefore made an attempt to evaluate the genetic cause of azoospermia, Y chromosome deletion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13e85917bb53aaadf6b5d549fe706ed
https://doi.org/10.1002/j.1939-4640.2003.tb02710.x
https://doi.org/10.1002/j.1939-4640.2003.tb02710.x
Autor:
Kumarasamy Thangaraj, S.R. Deepa, P. Reddy, Kadupu Pavani, Alla G. Reddy, Nalini J. Gupta, Baidyanath Chakravarty, Lalji Singh
Publikováno v:
International journal of andrology. 29(5)
Summary The autosomal DAZL (Deleted-in-Azoospermic-Like) gene, mapped to the short arm of the human chromosome 3, is the precursor for the Y-chromosomal DAZ cluster, which encodes for putative RNA-binding proteins. Mutations in the DAZL have been rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b4711ecb5a6ff91d29137ba6d71ad40
https://pubmed.ncbi.nlm.nih.gov/16573709
https://pubmed.ncbi.nlm.nih.gov/16573709