Articles with public access mandates - Aaron ChaplaLearn more
Available somewhere: 10
Maturity onset diabetes of the young in India–a distinctive mutation pattern identified through targeted next‐generation sequencing
A Chapla, MD Mruthyunjaya, HS Asha, D Varghese, M Varshney, ...
Clinical Endocrinology 82 (4), 533-542, 2015
Mandates: Council of Scientific and Industrial Research, India
Nuclear factor (NF)‐κB and its associated pathways are major molecular regulators of blood‐induced joint damage in a murine model of hemophilia
D Sen, A Chapla, N Walter, V Daniel, A Srivastava, GR Jayandharan
Journal of Thrombosis and Haemostasis 11 (2), 293-306, 2013
Mandates: Department of Biotechnology, India, Department of Science & Technology, India
Comprehensive maturity onset diabetes of the young (MODY) gene screening in pregnant women with diabetes in India
M Doddabelavangala Mruthyunjaya, A Chapla, ...
PLoS One 12 (1), e0168656, 2017
Mandates: Department of Biotechnology, India
An atypical form of diabetes among individuals with low BMI
E Lontchi-Yimagou, R Dasgupta, S Anoop, S Kehlenbrink, S Koppaka, ...
Diabetes Care 45 (6), 1428-1437, 2022
Mandates: US National Institutes of Health
Association of genetic variants with response to iron supplements in pregnancy
R Athiyarath, K Shaktivel, V Abraham, D Singh, JD Bondu, A Chapla, ...
Genes & Nutrition 10, 1-8, 2015
Mandates: Council of Scientific and Industrial Research, India, Department of …
ADAMTS13 missense variants associated with defective activity and secretion of ADAMTS13 in a patient with non-cirrhotic portal hypertension
A Goel, V Raghupathy, GJ Amirtharaj, A Chapla, A Venkatraman, ...
Indian Journal of Gastroenterology 36, 380-389, 2017
Mandates: Department of Science & Technology, India
WFS1 Gene–associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India
A Chapla, J Johnson, S Korula, N Mohan, A Ahmed, D Varghese, ...
The Journal of Clinical Endocrinology & Metabolism 107 (5), 1328-1336, 2022
Mandates: Department of Biotechnology, India
Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal Hyperplasia
L Ravichandran, D Varghese, R Parthiban, S Korula, N Thomas, ...
MethodsX 9, 101748, 2022
Mandates: Department of Science & Technology, India
Congenital Adrenal Hyperplasia–A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India
L Ravichandran, HS Asha, S Mathai, N Thomas, A Chapla
Indian Journal of Endocrinology and Metabolism 28 (2), 117-128, 2024
Mandates: Department of Science & Technology, India
High carrier frequency of CYP21A2 gene mutations in Southern India – underscoring the need for genetic testing in Congenital Adrenal Hyperplasia
L Ravichandran, S Paul, A HS, S Mathai, A Simon, S Danda, N Thomas, ...
Endocrine, 1-7, 2024
Mandates: Department of Science & Technology, India
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