Nallari P - Search Results

1

Mitochondrial DNA haplogroup 'R' is associated with Noonan syndrome of south India.

Rani DS, Dhandapany PS, Nallari P, Govindaraj P, Singh L, Thangaraj K. Rani DS, et al. Among authors: nallari p. Mitochondrion. 2010 Mar;10(2):166-73. doi: 10.1016/j.mito.2009.12.146. Epub 2009 Dec 16. Mitochondrion. 2010. PMID: 20006740

2

Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients.

Rani DS, Nallari P, Dhandapany PS, Tamilarasi S, Shah A, Archana V, AshokKumar M, Narasimhan C, Singh L, Thangaraj K. Rani DS, et al. Among authors: nallari p. DNA Cell Biol. 2012 Apr;31(4):616-24. doi: 10.1089/dna.2011.1366. Epub 2011 Oct 21. DNA Cell Biol. 2012. PMID: 22017532

3

High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.

Rani DS, Nallari P, Priyamvada S, Narasimhan C, Singh L, Thangaraj K. Rani DS, et al. Among authors: nallari p. BMC Med Genet. 2012 Aug 10;13:69. doi: 10.1186/1471-2350-13-69. BMC Med Genet. 2012. PMID: 22876777 Free PMC article.

4

A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM).

Rani DS, Dhandapany PS, Nallari P, Narasimhan C, Thangaraj K. Rani DS, et al. Among authors: nallari p. PLoS One. 2014 Jul 3;9(7):e101451. doi: 10.1371/journal.pone.0101451. eCollection 2014. PLoS One. 2014. PMID: 24992688 Free PMC article.

5

Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.

Selvi Rani D, Nallari P, Dhandapany PS, Rani J, Meraj K, Ganesan M, Narasimhan C, Thangaraj K. Selvi Rani D, et al. Among authors: nallari p. DNA Cell Biol. 2015 May;34(5):350-9. doi: 10.1089/dna.2014.2650. Epub 2015 Jan 21. DNA Cell Biol. 2015. PMID: 25607779

6

A Complete Absence of Missense Mutation in Myosin Regulatory and Essential Light Chain Genes of South Indian Hypertrophic and Dilated Cardiomyopathies.

Rani DS, Nallari P, Rani J, Nizamuddin S, Seelamneni T, Narasimhan C, Thangaraj K. Rani DS, et al. Among authors: nallari p. Cardiology. 2018;141(3):156-166. doi: 10.1159/000495027. Epub 2019 Jan 3. Cardiology. 2018. PMID: 30605904

7

Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy.

Rani DS, Vijaya Kumar A, Nallari P, Sampathkumar K, Dhandapany PS, Narasimhan C, Rathinavel A, Thangaraj K. Rani DS, et al. Among authors: nallari p. CJC Open. 2021 Aug 8;4(1):1-11. doi: 10.1016/j.cjco.2021.07.020. eCollection 2022 Jan. CJC Open. 2021. PMID: 35072022 Free PMC article.

8

Novel mutations of KCNQ1 in Long QT syndrome.

Qureshi SF, Ali A, Ananthapur V, Jayakrishnan MP, Calambur N, Thangaraj K, Nallari P. Qureshi SF, et al. Among authors: nallari p. Indian Heart J. 2013 Sep-Oct;65(5):552-60. doi: 10.1016/j.ihj.2013.08.025. Epub 2013 Sep 4. Indian Heart J. 2013. PMID: 24206879 Free PMC article. Review.

9

Germline study of AR gene of Indian women with ovarian failure.

Panda B, Rao L, Tosh D, Dixit H, Padmalatha V, Kanakavalli M, Raseswari T, Deenadayal M, Gupta N, Chakrabarty B, Nallari P, Singh L. Panda B, et al. Among authors: nallari p. Gynecol Endocrinol. 2011 Aug;27(8):572-8. doi: 10.3109/09513590.2010.507282. Epub 2010 Jul 30. Gynecol Endocrinol. 2011. PMID: 20672904 Free article.

10

Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome.

Ali A, Qureshi SF, Medikare V, Venkateshwari A, Calambur N, Rao H, Jayakrishnan MP, Shenthar J, Thangaraj K, Nallari P. Ali A, et al. Among authors: nallari p. J Interv Card Electrophysiol. 2016 Mar;45(2):119-30. doi: 10.1007/s10840-015-0082-5. Epub 2015 Dec 16. J Interv Card Electrophysiol. 2016. PMID: 26670457

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