10
results
for author:"Maheshwari M."
in Literature Citations
| The ubiquitin ligase E6-AP is induced and recruited to aggresomes in response to proteasome inhibition and may be involved in the ubiquitination of Hsp70-bound misfolded proteins. Mishra A., Godavarthi S.K., Maheshwari M., Goswami A., Jana N.R. J. Biol. Chem. 284:10537-10545(2009) · UniProtKB (1) · Mapped (6) |
| Common and rare variants of DAOA in bipolar disorder. Maheshwari M., Shi J., Badner J.A., Skol A., Willour V.L., Muzny D.M., Wheeler D.A., Gerald F.R., Detera-Wadleigh S., McMahon F.J. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B:960-966(2009) · Mapped (6) |
| Sequence variation in DOCK9 and heterogeneity in bipolar disorder. NIMH Genetics Initiative for Bipolar Disorder Consortium Psychiatr. Genet. 17:274-286(2007) · Mapped (18) |
| The DNA sequence, annotation and analysis of human chromosome 3. Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J., Chen R., Cree A., Ding Y. et al. Nature 440:1194-1198(2006) · UniProtKB (2,861) |
| The finished DNA sequence of human chromosome 12. Scherer S.E., Muzny D.M., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A. et al. Nature 440:346-351(2006) · UniProtKB (660) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,199) |
| Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario. Maheshwari M., Vijaya R., Ghosh M., Shastri S., Kabra M., Menon P.S. Am. J. Med. Genet. A 120A:180-184(2003) · Mapped (2) |
| Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. Hattori E., Liu C., Badner J.A., Bonner T.I., Christian S.L., Maheshwari M., Detera-Wadleigh S.D., Gibbs R.A., Gershon E.S. Am. J. Hum. Genet. 72:1131-1140(2003) · UniProtKB (4) · Mapped (2) |
| PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13. Maheshwari M., Belmont J., Fernbach S., Ho T., Molinari L., Yakub I., Yu F., Combes A., Towbin J.A., Craigen W.J. et al. |
| Prenatal diagnosis of haemoglobinopathies. Arora S., Kabra M., Maheshwari M., Shastri S., Kaur D., Deka D., Kriplani A., Menon P.S. Natl Med J India 14:340-342(2001) · Mapped (37) |
