Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Rakesh Kumar Panjaliya"'
Autor:
Jyotdeep Kour Raina, Rakesh Kumar Panjaliya, Vikas Dogra, Sushil Sharma, Anupriya, Parvinder Kumar
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-21 (2022)
Abstract Background The risk of Congenital Heart Defects (CHD) is greatly influenced by variants within the genes involved in folate-homocysteine metabolism. Polymorphism in MTHFR (C677T and G1793A) and MS/MTR (A2756G) genes increases the risk of dev
Externí odkaz:
https://doaj.org/article/db9320a7f18e4d0ab6a624b5c7c25478
Autor:
Jyotdeep Kour Raina, Minakashee Sharma, Rakesh Kumar Panjaliya, Vikas Dogra, Ashok Bakaya, Parvinder Kumar
Publikováno v:
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-13 (2020)
Abstract Background Coronary artery disease (CAD) is a complex disease resulting from the cumulative and interactive effects of large number of genes along with environmental exposure. Therefore, the present study was envisaged as an effort to study
Externí odkaz:
https://doaj.org/article/5868707a52434e58a313e7e2f52e4c85
Publikováno v:
Zootaxa. 5175:383-388
Jammuthrips paikulensis gen. et sp. n. is described from Jammu & Kashmir, Union territory of India and the morphological relationships among the closely related genera of subfamily Dendrothripinae are discussed. Key to Indian genera of subfamily Dend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0af8364d084345151d14acccd975b121
https://doi.org/10.11646/zootaxa.5175.3.5
https://doi.org/10.11646/zootaxa.5175.3.5
Autor:
Rakesh Kumar Panjaliya, Ashok Bakaya, Jyotdeep K. Raina, Parvinder Kumar, Vikas Dogra, Minakashee Sharma
Publikováno v:
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-13 (2020)
BMC Cardiovascular Disorders, Vol 20, Iss 1, Pp 1-13 (2020)
Background Coronary artery disease (CAD) is a complex disease resulting from the cumulative and interactive effects of large number of genes along with environmental exposure. Therefore, the present study was envisaged as an effort to study the assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f4d8f5cc3fd5fb478a5a6dee9a203df
https://doi.org/10.1186/s12872-020-01618-7
https://doi.org/10.1186/s12872-020-01618-7
Autor:
Rakesh Kumar Panjaliya
Publikováno v:
INTERNATIONAL JOURNAL OF HUMAN GENETICS. 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caa5938f449c97be59a147b4d1c42944
https://doi.org/10.31901/24566330.2018/18.3.669
https://doi.org/10.31901/24566330.2018/18.3.669
Publikováno v:
International Journal of Human Genetics. 12:311-317
In present study, six Alu insertion/deletion polymorphisms (Alu ACE, Alu APO, Alu PV-92, Alu PLAT, Alu FXIIIB and Alu D1) were studied in five different populations ( Brahmins, Rajputs, Scheduled Castes, Gujjars and Jat Sikhs) of Jammu region. Blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bca8b8975427397400f63242f15ea932
https://doi.org/10.1080/09723757.2012.11886185
https://doi.org/10.1080/09723757.2012.11886185
Publikováno v:
Journal of Diabetes & Metabolism.
Objective: Type 2 Diabetes is an increasingly common serious, metabolic disorder with a substantial inherited component. We examined 4 SNPs in 4 candidate genes for association with diabetes status and related phenotype in 800 individuals in a case c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef8fccdb405f68ee3e7a67ea15ebbf89
https://doi.org/10.4172/2155-6156.1000531
https://doi.org/10.4172/2155-6156.1000531
Autor:
Rakesh Kumar Panjaliya
Publikováno v:
INTERNATIONAL JOURNAL OF HUMAN GENETICS. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1a9d3273b2dc3b148c732e78bc807e4
https://doi.org/10.31901/24566330.2012/12.04.03
https://doi.org/10.31901/24566330.2012/12.04.03
Autor:
Parvinder Kumar, Jyotdeep K. Raina, Ravi Sharma, Ashok Bakaya, Minakshi Bhagat, Minakashee Sharma, Rakesh Kumar Panjaliya
Publikováno v:
Indian Heart Journal, Vol 68, Iss 3, Pp 421-430 (2016)
Aim: Potent risk factors at both genetic and non-genetic levels are accountable for susceptibility and instigation of different cardiovascular phenotypes. Recently, homocysteine is being identified as an important predictor for cardiovascular disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab68f62234e6490a79171cbed5367048