Bhattacharyya NP - Search Results

1

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. Among authors: bhattacharyya np. 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

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. Among authors: bhattacharyya np. 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

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. Among authors: bhattacharyya np. Hum Genet. 2000 Jun;106(6):597-604. doi: 10.1007/s004390000320. Hum Genet. 2000. PMID: 10942107

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: bhattacharyya np. Eur J Hum Genet. 2000 Sep;8(9):678-82. doi: 10.1038/sj.ejhg.5200515. Eur J Hum Genet. 2000. PMID: 10980573

5

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. Among authors: bhattacharyya np. Hum Genet. 2001 Apr;108(4):310-7. doi: 10.1007/s004390100479. Hum Genet. 2001. PMID: 11379877

6

Molecular analysis of GAA repeats and four linked bi-allelic markers in and around the frataxin gene in patients and normal populations from India.

Chattopadhyay B, Gupta S, Gangopadhyay PK, Das SK, Roy T, Mukherjee SC, Sinha KK, Singhal BS, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: bhattacharyya np. Ann Hum Genet. 2004 May;68(Pt 3):189-95. doi: 10.1046/j.1529-8817.2003.00087.x. Ann Hum Genet. 2004. PMID: 15180699

7

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India.

Chattopadhyay B, Ghosh S, Gangopadhyay PK, Das SK, Roy T, Sinha KK, Jha DK, Mukherjee SC, Chakraborty A, Singhal BS, Bhattacharya AK, Bhattacharyya NP. Chattopadhyay B, et al. Among authors: bhattacharyya np. Neurosci Lett. 2003 Jul 17;345(2):93-6. doi: 10.1016/s0304-3940(03)00436-1. Neurosci Lett. 2003. PMID: 12821179

8

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. Genome Res. 1999 Aug;9(8):711-9. Genome Res. 1999. PMID: 10447506 Free article.

9

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: bhattacharyya np. Acta Neurol Scand. 2003 Dec;108(6):407-14. doi: 10.1034/j.1600-0404.2003.00167.x. Acta Neurol Scand. 2003. PMID: 14616293

10

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: bhattacharyya np. Neurol India. 1998 Jul-Sep;46(3):199-203. Neurol India. 1998. PMID: 29508777 Free article.

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