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Number of items: 3.

Journal Article

Singh, Nivedita and Kallollimath, Pradeep and Shah, Mohd Hussain and Kapoor, Saketh and Bhat, Vishwanath Kumble and Viswanathan, Lakshminarayanapuram Gopal and Nagappa, Madhu and Bindu, Parayil S and Taly, Arun B and Sinha, Sanjib and Kumar, Arun (2019) Genetic analysis of ATP7B in 102 south Indian families with Wilson disease. In: PLOS ONE, 14 (5).

Singh, Nivedita and Bhat, Vishwanath Kumble and Tiwari, Ankana and Kodaganur, Srinivas G and Tontanahal, Sagar J and Sarda, Astha and Malini, K V and Kumar, Arun (2017) A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family. In: HUMAN MOLECULAR GENETICS, 26 (6). pp. 1104-1114.

Pradhan, Shalmali Avinash and Rather, Mohammad Iqbal and Tiwari, Ankana and Bhat, Vishwanath Kumble and Kumar, Arun (2014) Evidence that TSC2 acts as a transcription factor and binds to and represses the promoter of Epiregulin. In: NUCLEIC ACIDS RESEARCH, 42 (10). pp. 6243-6255.

This list was generated on Wed Oct 16 08:11:52 2019 IST.