Associated Papers
Whole-exome sequencing for identification of specific gene mutations in an Indian cohort of triple-negative breast cancer patients.
Preeti P et al.
Discover Oncology, 2025
41324770 (PubMed )
Supplement: 12672_2025_3921_MOESM2_ESM.xlsx › Sheet1
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
Venkatesh SK et al.
Psychiatric Genetics, 2014
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.
González-Pérez P et al.
Neurology, 2012
Electrostatic suppression allows tyrosine site-specific recombination in the absence of a conserved catalytic arginine.
Rowley PA et al.
The Journal of Biological Chemistry, 2010
Stepwise propagation of the ATP-induced conformational change of the F1-ATPase beta subunit revealed by NMR.
Yagi H et al.
The Journal of Biological Chemistry, 2009
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