Items where Subject is "Biochemistry,Cell and Molecular Signalling > Genomics in Diabetes"
Group by: Creators | Item Type
Number of items at this level: 9.
Alvarez-Silva, Camila and Kashani, Alireza and Hansen, Tue Haldor and Pinna, Nishal Kumar and Anjana, R M and Dutta, Anirban and Saxena, Shruti and Støy, Julie and Kampmann, Ulla and Nielsen, Trine and Jørgensen, Torben and Gnanaprakash, V and Gnanavadivel, R and Sukumaran, Aswath and Rani, C S S and Færch, Kristine and Radha, V and Balasubramanyam, M and Nair, Gopinath Balakrish and Das, Bhabatosh and Vestergaard, Henrik and Hansen, Torben and Mande, Sharmila Shekhar and Mohan, V and Arumugam, Manimozhiyan and Pedersen, Oluf (2021) Trans-ethnic gut microbiota signatures of type 2 diabetes in Denmark and India. Genome Medicine, 13 (1). ISSN 1756-994X
Balasubramanyam, M and Balaji, R A and Subashini, B and Mohan, V (2001) Evidence for mechanistic alterations of Ca2+ homeostasis in Type 2 diabetes mellitus. International journal of experimental diabetes research, 1 (4). pp. 275-87. ISSN 1560-4284
Bodhini, D and Radha, V and Dhar, M and NIarayani, N and Mohan, V (2007) The rs12255372(G/T) and rs7903146(C/T) polymorphisms of the TCF7L2 gene are associated with type 2 diabetes mellitus in Asian Indians. Metabolism, 56 (9). pp. 1174-78. ISSN 00260495
Mohan, V and Balasubramanyam, M and Radha, V (2005) Genomics and Proteomics of Type 2 Diabetes in Indians. The Journal of the Association of Physicians of India, 53 (6). pp. 507-509.
Mohan, V and Radha, V (2019) Precision Diabetes Is Slowly Becoming a Reality. Medical Principles and Practice, 28 (1). p. 1. ISSN 1011-7571
Omkar, P and Ravikumar, KG and Gopi, S and Raman, T and Radha, V and Mohan, V (2020) Thiamine-responsive megaloblastic anemia syndrome: A case report. Journal of Diabetology, 11 (1). p. 45. ISSN 2078-7685
Poovazhagi, V and Mohan, V (2014) Neonatal Diabetes. RSSDI TEXTBOOK OF DIABETES MELLITUS .
Radha, V and Ramya, B and Gopi, S and Kavitha, B and Preetika, S and Thai, K and Unnikrishnan, R and Mohan, V and Gupta, P K (2018) Successful transition to sulphonylurea therapy from insulin in a child with permanent neonatal diabetes due to a KCNJ11 gene mutation. Journal of Diabetology, 9 (2). p. 65. ISSN 2078-7685
Wall, JD and Stawiski, EW and Ratan, A and Radha, V and Mohan, V and Peeterson, AS (2019) The GenomeAsia 100K Project enables genetic discoveries across Asia. Nature, 576 (7785). p. 106. ISSN 0028-0836