Basu P - Search Results

1

Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.

Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP. Basu P, et al. Hum Genet. 2000 Jun;106(6):597-604. doi: 10.1007/s004390000320. Hum Genet. 2000. PMID: 10942107

2

Expansion of CTG repeat in myotonin protein kinase gene on Alu(ins)-HinfI-I background in a myotonic dystrophy patient from India. Mutations in brief no. 210. Online.

Basu P, Gangopadhaya PK, Murkherjee SC, Sinha KK, Bhattacharyya NP. Basu P, et al. Hum Mutat. 1999;13(1):84. doi: 10.1002/(SICI)1098-1004(1999)13:1<84::AID-HUMU15>3.0.CO;2-U. Hum Mutat. 1999. PMID: 10189221

3

Negligible male gene flow across ethnic boundaries in India, revealed by analysis of Y-chromosomal DNA polymorphisms.

Bhattacharyya NP, Basu P, Das M, Pramanik S, Banerjee R, Roy B, Roychoudhury S, Majumder PP. Bhattacharyya NP, et al. Among authors: basu p. Genome Res. 1999 Aug;9(8):711-9. Genome Res. 1999. PMID: 10447506 Free article.

4

Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India.

Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, Jha DK, Sinha S, Das SK, Maity BK, Mukherjee SC, Roychoudhuri S, Majumder PP, Bhattacharyya NP. Pramanik S, et al. Among authors: basu p. Eur J Hum Genet. 2000 Sep;8(9):678-82. doi: 10.1038/sj.ejhg.5200515. Eur J Hum Genet. 2000. PMID: 10980573

5

Molecular anatomy of CTG expansion in myotonin protein kinase gene among myotonic dystrophy patients from eastern India.

Basu P, Gangopadhaya PK, Mukherjee SC, Das SK, Sinha KK, Bhattacharyya NP. Basu P, et al. Hum Mutat. 2000 Oct;16(4):372. doi: 10.1002/1098-1004(200010)16:4<372::AID-HUMU13>3.0.CO;2-G. Hum Mutat. 2000. PMID: 11013451

6

Haplotype analysis of genomic polymorphisms in and around the myotonic dystrophy locus in diverse populations of India.

Basu P, Majumder PP, Roychoudhury S, Bhattacharyya NP. Basu P, et al. Hum Genet. 2001 Apr;108(4):310-7. doi: 10.1007/s004390100479. Hum Genet. 2001. PMID: 11379877

7

Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India.

Chattopadhyay B, Basu P, Gangopadhyay PK, Mukherjee SC, Sinha KK, Chakraborty A, Roy T, Roychoudhury S, Majumder PP, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: basu p. Acta Neurol Scand. 2003 Dec;108(6):407-14. doi: 10.1034/j.1600-0404.2003.00167.x. Acta Neurol Scand. 2003. PMID: 14616293

8

Molecular diagnosis of myotonic dystrophy and Huntington's disease from Calcutta, India.

Basu P, Gunguly PK, Basu D, Bhattacharyya NP, Bhattacharya NP. Basu P, et al. Among authors: basu d. Neurol India. 1998 Jul-Sep;46(3):199-203. Neurol India. 1998. PMID: 29508777 Free article.

9

Comparative analyses of genetic risk prediction methods reveal extreme diversity of genetic predisposition to nonalcoholic fatty liver disease (NAFLD) among ethnic populations of India.

Chatterjee A, Basu A, Chowdhury A, Das K, Sarkar-Roy N, Majumder PP, Basu P. Chatterjee A, et al. Among authors: basu a, basu p. J Genet. 2015 Mar;94(1):105-13. doi: 10.1007/s12041-015-0494-0. J Genet. 2015. PMID: 25846882

10

Hepatic transcriptome signature correlated with HOMA-IR explains early nonalcoholic fatty liver disease pathogenesis.

Chatterjee A, Basu A, Das K, Singh P, Mondal D, Bhattacharya B, Roychoudhury S, Majumder PP, Chowdhury A, Basu P. Chatterjee A, et al. Among authors: basu a, basu p. Ann Hepatol. 2020 Sep-Oct;19(5):472-481. doi: 10.1016/j.aohep.2020.06.009. Epub 2020 Jul 15. Ann Hepatol. 2020. PMID: 32682086 Free article.

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