Singh N - Search Results

1

Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.

Singh N, Kallollimath P, Shah MH, Kapoor S, Bhat VK, Viswanathan LG, Nagappa M, Bindu PS, Taly AB, Sinha S, Kumar A. Singh N, et al. PLoS One. 2019 May 6;14(5):e0215779. doi: 10.1371/journal.pone.0215779. eCollection 2019. PLoS One. 2019. PMID: 31059521 Free PMC article.

2

Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India.

Nagappa M, Sinha S, Saini JS, Kallolimath P, Singh N, Kumar A, Bindu PS, Taly AB. Nagappa M, et al. Among authors: singh n. J Clin Neurosci. 2016 May;27:91-4. doi: 10.1016/j.jocn.2015.06.035. Epub 2016 Jan 4. J Clin Neurosci. 2016. PMID: 26765764

3

Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.

Kapoor S, Shah MH, Singh N, Rather MI, Bhat V, Gopinath S, Bindu PS, Taly AB, Sinha S, Nagappa M, Bharath RD, Mahadevan A, Narayanappa G, Chickabasaviah YT, Kumar A. Kapoor S, et al. Among authors: singh n. PLoS One. 2016 May 19;11(5):e0155605. doi: 10.1371/journal.pone.0155605. eCollection 2016. PLoS One. 2016. PMID: 27196560 Free PMC article.

4

A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family.

Singh N, Kumble Bhat V, Tiwari A, Kodaganur SG, Tontanahal SJ, Sarda A, Malini KV, Kumar A. Singh N, et al. Hum Mol Genet. 2017 Mar 15;26(6):1104-1114. doi: 10.1093/hmg/ddx020. Hum Mol Genet. 2017. PMID: 28087737

5

Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families.

Madhangi M, Dutta D, Show S, Bhat VK, Rather MI, Tiwari A, Singh N, Duvvari MR, Murthy GJ, Kumar A, Nongthomba U. Madhangi M, et al. Among authors: singh n. Hum Mol Genet. 2021 Apr 30;30(6):467-484. doi: 10.1093/hmg/ddab061. Hum Mol Genet. 2021. PMID: 33693649

6

Alteration in synaptic nanoscale organization dictates amyloidogenic processing in Alzheimer's disease.

Kedia S, Ramakrishna P, Netrakanti PR, Singh N, Sisodia SS, Jose M, Kumar S, Mahadevan A, Ramanan N, Nadkarni S, Nair D. Kedia S, et al. Among authors: singh n. iScience. 2020 Dec 11;24(1):101924. doi: 10.1016/j.isci.2020.101924. eCollection 2021 Jan 22. iScience. 2020. PMID: 33409475 Free PMC article.

7

Achieving nanoscale precision using neuromorphic localization microscopy.

Mangalwedhekar R, Singh N, Thakur CS, Seelamantula CS, Jose M, Nair D. Mangalwedhekar R, et al. Among authors: singh n. Nat Nanotechnol. 2023 Apr;18(4):380-389. doi: 10.1038/s41565-022-01291-1. Epub 2023 Jan 23. Nat Nanotechnol. 2023. PMID: 36690737

8

Identification of Xanthine Derivatives as Inhibitors of Phosphodiesterase 9A Through In silico and Biological Studies.

Singh N, Patra S, Patra S. Singh N, et al. Comb Chem High Throughput Screen. 2018;21(7):476-486. doi: 10.2174/1386207321666180821100713. Comb Chem High Throughput Screen. 2018. PMID: 30129405

9

Neuronal PET tracers for Alzheimer's disease.

Prem Kumar A, Singh N, Nair D, Justin A. Prem Kumar A, et al. Among authors: singh n. Biochem Biophys Res Commun. 2022 Jan 8;587:58-62. doi: 10.1016/j.bbrc.2021.11.093. Epub 2021 Nov 30. Biochem Biophys Res Commun. 2022. PMID: 34864547 Review.

10

Nanoscale regulation of Ca²⁺ dependent phase transitions and real-time dynamics of SAP97/hDLG.

Rajeev P, Singh N, Kechkar A, Butler C, Ramanan N, Sibarita JB, Jose M, Nair D. Rajeev P, et al. Among authors: singh n. Nat Commun. 2022 Jul 22;13(1):4236. doi: 10.1038/s41467-022-31912-1. Nat Commun. 2022. PMID: 35869063 Free PMC article.

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