Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Pavithra Amritkumar"'
Autor:
Jeffrey Justin Margret, Chandru Jayasankaran, Pavithra Amritkumar, Hela Azaiez, C. R. Srikumari Srisailapathy
Publikováno v:
Advanced Genetics, Vol 5, Iss 2, Pp n/a-n/a (2024)
Abstract The co‐occurrence of sensorineural hearing loss and male infertility has been reported in several instances, suggesting potential shared genetic underpinnings. One such example is the contiguous gene deletion of CATSPER2 and STRC genes, pr
Externí odkaz:
https://doaj.org/article/ba7948f06d9b450aa3b2df100df05b13
Autor:
Pavithra Amritkumar, Justin Margret Jeffrey, Jayasankaran Chandru, Paridhy Vanniya S, M. Kalaimathi, Rajagopalan Ramakrishnan, N. P. Karthikeyen, C. R. Srikumari Srisailapathy
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-24 (2018)
Abstract Background DFNB1, the first locus to have been associated with deafness, has two major genes GJB2 & GJB6, whose mutations have played vital role in hearing impairment across many ethnicities in the world. In our present study we have focused
Externí odkaz:
https://doaj.org/article/8e140fa3577c452ba05f12832f18e30b
Autor:
Jeffrey, Justin Margret, Chandru, Jayasankaran, Pavithra, Amritkumar, Kalaimathi, Murugesan, Indhumathi, Nagarathinam, Ashraf, Pangadan, Srisailapathy, C. R. Srikumari
Publikováno v:
Current Science, 2018 Jun . 114(12), 2538-2542.
Externí odkaz:
https://www.jstor.org/stable/26495768
Autor:
Pavithra Amritkumar, Hemalakshmi R
Publikováno v:
International Journal of Research in Pharmaceutical Sciences. 12:2095-2114
Autism spectrum disorder (ASD) is a developmental disorder that affects behaviour and communication. It can be diagnosed at any age, although the symptoms generally appear in the first two years of life. Autism is also known as a "spectrum" disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::126c557fcf71af8f5a7487b81726997b
https://doi.org/10.26452/ijrps.v12i3.4820
https://doi.org/10.26452/ijrps.v12i3.4820
Unravelling the mechanism of non-syndromic hearing loss (NSHL) through genetic studies have till date been perplexed by several factors such as genetic heterogeneity, multiple phenotypes, consanguinity and marriages between hearing impaired persons.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f94c40dc58f3df07e22459733bc7465d
https://doi.org/10.9734/bpi/nfmmr/v1/3292f
https://doi.org/10.9734/bpi/nfmmr/v1/3292f
Publikováno v:
Microbiome-Host Interactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f1f8671d1880fc8dfcd946eb52545d8
https://doi.org/10.1201/9781003037521-13
https://doi.org/10.1201/9781003037521-13
Autor:
N. P. Karthikeyen, Murugesan Kalaimathi, Jayasankaran Chandru, Paridhy Vanniya. S, C. R. Srikumari Srisailapathy, Rajagopalan Ramakrishnan, Pavithra Amritkumar, Justin Margret Jeffrey
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-24 (2018)
BMC Medical Genetics
BMC Medical Genetics
Background DFNB1, the first locus to have been associated with deafness, has two major genes GJB2 & GJB6, whose mutations have played vital role in hearing impairment across many ethnicities in the world. In our present study we have focused on the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62133fe99b7556264bc036152c118a9c
http://link.springer.com/article/10.1186/s12881-018-0609-6
http://link.springer.com/article/10.1186/s12881-018-0609-6
Akademický článek
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Publikováno v:
SN Applied Sciences. 1
Alarming rate of environmental pollution caused by single-use plastics has necessitated the search for developing sustainable yet, cost-effective alternatives. This study aimed to develop bioplastic films using combination of jackfruit waste flour an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f2bc27087f4cad56573d12c548efe99
https://doi.org/10.1007/s42452-019-1460-x
https://doi.org/10.1007/s42452-019-1460-x
Autor:
Pavithra, Amritkumar1, Selvakumari, Mathiyalagan1, Nityaa, Venkatesan1, Sharanya, Narasimhan1, Ramakrishnan, Rajagopalan2, Narasimhan, Murali3, Srisailapathy, C.R. Srikumari1
Publikováno v:
Annals of Human Genetics. Jan2015, Vol. 79 Issue 1, p1-82. 7p.