Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.

Neurol Genet. 2017 3(3):e149.

2017

3`-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk.

Clin Chim Acta. 471:46-54.

2017

Origin and spread of human mitochondrial DNA haplogroup U7.

Sci Rep; 7:46044.

2017

Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent.

PLoS One. 12:e0164823.

2017

Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond.

Eur J Hum Genet. 25:493-498.

2017

Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation.

J Invest Dermatol. 137:670-677.

2017

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.

Mitochondrion 32:42-49.

2017

Leber\\\'s Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India

Invest. Ophthalmol. Vis. Sci. 58: 3923-3930

2017

Mutations in the prostate specific antigen (PSA/KLK3) correlate with male infertility

Sci. Rep. 7:11225

2017

MSDB:A Comperhensive Database of Simple Sequence Repeats

Genome Biol Evol

2017

Simple Sequence repeats showing \\\"length preference have regulatory functions in humans.\\\"

Gene

2017

Ultraconserved sequences associated with HoxD cluster have strong repression activity.

Genome Biol Evol

2017

O-GlcNAcylation of Boundary melanogaster correlates with active histone marks at the promoters of its target genes

Nucleus

2017

C-State: An interactive web app for simultaneous multi-gene visualization and comparative epigenetic pattern search

BMC Bioinformatics

2017

Vertebrate GAF/ThPOK: emerging functions in chromatin architecture and transcriptional regulation.

Cell Mol Life Sci. 2017 Aug 30.

2017