Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Padma, Tirunilai"'
Autor:
Mamata Manne, Sridhar Gunde, Ravi Kumar Reddy Kondreddy, Nagaraju Thurlapati, Padma Tirunilai
Publikováno v:
Oman Journal of Ophthalmology, Vol 5, Iss 1, Pp 32-36 (2012)
Aim: Exposure to UV light is the major risk factor in the development of age-related cataract (ARC). UV filters produced during tryptophan catabolism maintain the transparency of the lens and protect retina from photo damage. Indoleamine 2, 3-dioxyge
Externí odkaz:
https://doaj.org/article/fab144376cf146a8aca227ea3e24d09d
Autor:
Ravi Kumar Reddy Kondareddy, Padma Tirunilai, Syed Saifuddin Adeel, Padma Gunda, Mamata Manne
Publikováno v:
Journal of Genetics. 97:879-885
The aim of this studywas to identify the gene causing bilateral autosomal dominant zonular congenital cataract (ADZCC) without pulverulent opacities in an extended Muslim family by exome sequencing and subsequent analysis. An extended family of 37 me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a2e544a51e0354a53e37df6d9f6c400
https://doi.org/10.1007/s12041-018-0971-3
https://doi.org/10.1007/s12041-018-0971-3
Publikováno v:
Clinical and Experimental Hypertension. 38:520-525
Angiotensinogen (AGT) is one of the candidate genes that has been extensively investigated for association of its variants with essential hypertension. Studies focusing on the contribution of tagged single nucleotide polymorphisms (SNPs) in the AGT g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffc0728e986f0b292093de4ca31e5148
https://doi.org/10.3109/10641963.2016.1163371
https://doi.org/10.3109/10641963.2016.1163371
Autor:
Padma, Gunda, Mamata, Manne, Syed Saifuddin, Adeel, Ravi Kumar Reddy, Kondareddy, Padma, Tirunilai
Publikováno v:
Journal of genetics. 97(4)
The aim of this studywas to identify the gene causing bilateral autosomal dominant zonular congenital cataract (ADZCC) without pulverulent opacities in an extended Muslim family by exome sequencing and subsequent analysis. An extended family of 37 me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa999b0fbf0310f9e36b93dd3a511b94
https://pubmed.ncbi.nlm.nih.gov/30262699
https://pubmed.ncbi.nlm.nih.gov/30262699
Publikováno v:
Clinical and Experimental Hypertension. 34:230-235
Introduction. Bradykinin, a vasodilator by nature has been documented to have a protective role against hypertension and cardiovascular complications. Polymorphisms of bradykinin B2 receptor (BDKRB2) gene are reported to be predisposing factors for h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b739cdafd01e8bc79ac57b9ee648ff3
https://doi.org/10.3109/10641963.2011.631653
https://doi.org/10.3109/10641963.2011.631653
Autor:
Padma Tirunilai, Nagaraju Thurlapati, Sridhar Gunde, Mamata Manne, Ravi Kumar Reddy Kondreddy
Publikováno v:
Oman Journal of Ophthalmology, Vol 5, Iss 1, Pp 32-36 (2012)
Oman Journal of Ophthalmology
Oman Journal of Ophthalmology
Aim: Exposure to UV light is the major risk factor in the development of age-related cataract (ARC). UV filters produced during tryptophan catabolism maintain the transparency of the lens and protect retina from photo damage. Indoleamine 2, 3-dioxyge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::550dd49dc59c905b3794f0d46b818187
http://www.ojoonline.org/article.asp?issn=0974-620X
http://www.ojoonline.org/article.asp?issn=0974-620X
Publikováno v:
Clinical and experimental hypertension (New York, N.Y. : 1993). 36(6)
Leptin and leptin receptor gene polymorphisms have been associated with obesity; however, their association with blood pressure has not been fully elucidated. The aim of this study was to examine the effect of tetranucleotide repeat polymorphism in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a58fee9d24131d78552d552421647406
https://pubmed.ncbi.nlm.nih.gov/24171506
https://pubmed.ncbi.nlm.nih.gov/24171506
Akademický článek
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Autor:
Padma Tirunilai, Padma Gunda
Publikováno v:
Genetics and Pathophysiology of Essential Hypertension
Human genome encompasses several thousands of genes which when fail to function normally lead to a defective phenotype expressed sometimes as a disease or disorder. These diseases or disorders may be simple or complex depending upon the nature and nu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13fd32c6a2b965caabd31d2eb56732c6
https://doi.org/10.5772/31542
https://doi.org/10.5772/31542
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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