Výsledky vyhledávání - "G. R. Chandak"

Akademický článek

Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier

Publikováno v: Journal of Obesity, Vol 2011 (2011)

Few studies have investigated the association between genetic variation and obesity traits in Indian populations or the role of environmental factors as modifiers of these relationships. In the context of rapid urbanisation, resulting in significant

Externí odkaz: https://doaj.org/article/e8354c422ead4df595bb66399f3d3700

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Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis

Autor: G R Chandak, Sadaranga Andal Bhaskar, Lalji Singh, Mohammed M. Idris, Parupudi V.J. Sriram, Duvvuru Nageshwar Reddy

Publikováno v: Journal of Medical Genetics. 39:347-351

Pancreatitis is a global health care problem with varied aetiologies. Alcoholism is responsible in the majority of patients while other causes, such as heredity, gallstones, hyperlipidaemia, hypercalcaemia, and idiopathic pancreatitis, are relatively

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8f08f8870cdba01d7d045f03a5988cf7
https://doi.org/10.1136/jmg.39.5.347

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Analysis of 32 common susceptibility genetic variants and their combined effect in predicting risk of Type 2 diabetes and related traits in Indians

Autor: C S, Janipalli, M V K, Kumar, D G, Vinay, M N, Sandeep, S, Bhaskar, S R, Kulkarni, M, Aruna, C V, Joglekar, S, Priyadharshini, N, Maheshwari, C S, Yajnik, G R, Chandak

Publikováno v: Diabetic medicine : a journal of the British Diabetic Association. 29(1)

Recent genome-wide association studies have identified several Type 2 diabetes-related loci. We investigated the effect of susceptibility genetic variants, individually, together and in combination with conventional risk factors, on Type 2 diabetes a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1a99829dc4bc6206d72fbddb680a75ab
https://pubmed.ncbi.nlm.nih.gov/21913964

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A set of five microsatellite markers linked to F8 gene can detect haemophilia A carriers across India

Autor: A, Saha, S, Nayak, K R, Mani, G R, Chandak, K, Ray, A, Mukhopadhyay

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 17(5)

Haemophilia A (HA) is an X-linked recessive bleeding disorder, primarily because of defects in the 186-kb long factor VIII gene (F8) affecting 1-2 men per 10,000 worldwide. Available markers for carrier detection are not effective in all populations,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::48ddba73f2842dc4e27cd3e27750bd3e
https://pubmed.ncbi.nlm.nih.gov/21696518

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