Mittal U - Search Results

1

Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.

Mittal U, Roy S, Jain S, Srivastava AK, Mukerji M. Mittal U, et al. J Hum Genet. 2005;50(3):155-157. doi: 10.1007/s10038-005-0233-0. Epub 2005 Mar 5. J Hum Genet. 2005. PMID: 15750685

2

Evidence of a common founder for SCA12 in the Indian population.

Bahl S, Virdi K, Mittal U, Sachdeva MP, Kalla AK, Holmes SE, O'Hearn E, Margolis RL, Jain S, Srivastava AK, Mukerji M. Bahl S, et al. Among authors: mittal u. Ann Hum Genet. 2005 Sep;69(Pt 5):528-34. doi: 10.1046/j.1529-8817.2005.00173.x. Ann Hum Genet. 2005. PMID: 16138911

3

SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies.

Pandey N, Mittal U, Srivastava AK, Mukerji M. Pandey N, et al. Among authors: mittal u. J Hum Genet. 2004;49(11):596-602. doi: 10.1007/s10038-004-0194-8. Epub 2004 Sep 10. J Hum Genet. 2004. PMID: 15368101

4

Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies.

Mittal U, Srivastava AK, Jain S, Jain S, Mukerji M. Mittal U, et al. Arch Neurol. 2005 Apr;62(4):637-40. doi: 10.1001/archneur.62.4.637. Arch Neurol. 2005. PMID: 15824265

5

Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms.

Mittal U, Sharma S, Chopra R, Dheeraj K, Pal PK, Srivastava AK, Mukerji M. Mittal U, et al. Hum Genet. 2005 Oct;118(1):107-14. doi: 10.1007/s00439-005-0018-8. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16133185

6

Complex phenotypes in an Indian family with homozygous SCA2 mutations.

Ragothaman M, Sarangmath N, Chaudhary S, Khare V, Mittal U, Sharma S, Komatireddy S, Chakrabarti S, Mukerji M, Juyal RC, Thelma BK, Muthane UB. Ragothaman M, et al. Among authors: mittal u. Ann Neurol. 2004 Jan;55(1):130-3. doi: 10.1002/ana.10815. Ann Neurol. 2004. PMID: 14705123

7

SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.

Krishna N, Mohan S, Yashavantha BS, Rammurthy A, Kiran Kumar HB, Mittal U, Tyagi S, Mukerji M, Jain S, Pal PK, Purushottam M. Krishna N, et al. Among authors: mittal u. Indian J Med Res. 2007 Nov;126(5):465-70. Indian J Med Res. 2007. PMID: 18160752 Free article.

8

Genetic landscape of the people of India: a canvas for disease gene exploration.

Indian Genome Variation Consortium. Indian Genome Variation Consortium. J Genet. 2008 Apr;87(1):3-20. doi: 10.1007/s12041-008-0002-x. J Genet. 2008. PMID: 18560169 Free article.

9

EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda.

Aggarwal S, Negi S, Jha P, Singh PK, Stobdan T, Pasha MA, Ghosh S, Agrawal A; Indian Genome Variation Consortium; Prasher B, Mukerji M. Aggarwal S, et al. Proc Natl Acad Sci U S A. 2010 Nov 2;107(44):18961-6. doi: 10.1073/pnas.1006108107. Epub 2010 Oct 18. Proc Natl Acad Sci U S A. 2010. PMID: 20956315 Free PMC article.

10

Averting H⁺-Mediated Charge Storage Chemistry Stabilizes the High Output Voltage of LiMn₂O₄-Based Aqueous Battery.

Bhadra A, Swathilakshmi S, Mittal U, Sharma N, Sai Gautam G, Kundu D. Bhadra A, et al. Among authors: mittal u. Small Methods. 2024 Apr 19:e2400070. doi: 10.1002/smtd.202400070. Online ahead of print. Small Methods. 2024. PMID: 38639028

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

21 results

Search Page