Muhammad I. Khan-Imran

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

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Found 46 publications

Molecular and clinical analysis of 27 German patients with Leber congenital amaurosis.

Molecular and clinical analysis of 27 German patients with Leber congenital amaurosis.

Journal: PloS one

Published: September 19, 2018

Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides.

Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 19, 2018

Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa.

Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa.

Journal: PLoS genetics

Published: February 06, 2018

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.

Journal: Genes

Published: January 19, 2018

Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes.

Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate Genes.

Journal: Genes

Published: October 20, 2017

EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa.

EYS mutation update: In silico assessment of 271 reported and 26 novel variants in patients with retinitis pigmentosa.

Journal: Human mutation

Published: July 28, 2017

Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families

Homozygosity Mapping and Targeted Sanger Sequencing Identifies Three Novel CRB1 (Crumbs homologue 1) Mutations in Iranian Retinal Degeneration Families

Journal: Iranian biomedical journal

Published: May 04, 2017

Thalidomide attenuates development of morphine dependence in mice by inhibiting PI3K/Akt and nitric oxide signaling pathways.

Thalidomide attenuates development of morphine dependence in mice by inhibiting PI3K/Akt and nitric oxide signaling pathways.

Journal: Progress in neuro-psychopharmacology & biological psychiatry

Published: April 12, 2017

Variants in the PRPF8 Gene are Associated with Glaucoma.

Variants in the PRPF8 Gene are Associated with Glaucoma.

Journal: Molecular neurobiology

Published: March 29, 2017

Synthesis, docking study and neuroprotective effects of some novel pyrano[3,2-c]chromene derivatives bearing morpholine/phenylpiperazine moiety.

Synthesis, docking study and neuroprotective effects of some novel pyrano[3,2-c]chromene derivatives bearing morpholine/phenylpiperazine moiety.

Journal: Bioorganic & medicinal chemistry

Published: February 09, 2017

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Journal: Nature genetics

Published: September 30, 2016

Thalidomide attenuates the development and expression of antinociceptive tolerance to μ-opioid agonist morphine through l-arginine-iNOS and nitric oxide pathway.

Thalidomide attenuates the development and expression of antinociceptive tolerance to μ-opioid agonist morphine through l-arginine-iNOS and nitric oxide pathway.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: August 13, 2016

Showing 1-12 of 46

Last Updated: 09/26/2026