Shaheen N. Khan

87 West Canal Bank Road
Thokar, PB 53700, Pakistan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 62 publications

Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Journal: Nature genetics

Published: August 26, 2025

Human amniotic membrane as differentiating matrix for in vitro chondrogenesis.

Human amniotic membrane as differentiating matrix for in vitro chondrogenesis.

Journal: Regenerative medicine

Published: October 10, 2018

In vitro preconditioning of insulin-producing cells with growth factors improves their survival and ability to release insulin.

In vitro preconditioning of insulin-producing cells with growth factors improves their survival and ability to release insulin.

Journal: Journal of biosciences

Published: September 13, 2018

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.

Journal: Molecular psychiatry

Published: September 02, 2018

Human neonatal stem cell-derived skin substitute improves healing of severe burn wounds in a rat model.

Human neonatal stem cell-derived skin substitute improves healing of severe burn wounds in a rat model.

Journal: Cell biology international

Published: August 07, 2018

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.

Journal: Human mutation

Published: July 06, 2018

Whole-Exome Sequencing Identifies Novel Variants that Co-segregates with Autosomal Recessive Retinal Degeneration in a Pakistani Pedigree.

Whole-Exome Sequencing Identifies Novel Variants that Co-segregates with Autosomal Recessive Retinal Degeneration in a Pakistani Pedigree.

Journal: Advances in experimental medicine and biology

Published: May 04, 2018

Whole genome sequencing data for two individuals of Pakistani descent.

Whole genome sequencing data for two individuals of Pakistani descent.

Journal: Scientific data

Published: February 22, 2018

Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.

Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.

Journal: Journal of medical genetics

Published: December 16, 2017

Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse.

Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse.

Journal: PLoS genetics

Published: November 09, 2017

Serum from CCl4-induced acute rat injury model induces differentiation of ADSCs towards hepatic cells and reduces liver fibrosis.

Serum from CCl4-induced acute rat injury model induces differentiation of ADSCs towards hepatic cells and reduces liver fibrosis.

Journal: Growth factors (Chur, Switzerland)

Published: November 08, 2017

Transplantation of stromal-derived factor 1α and basic fibroblast growth factor primed insulin-producing cells reverses hyperglycaemia in diabetic rats.

Transplantation of stromal-derived factor 1α and basic fibroblast growth factor primed insulin-producing cells reverses hyperglycaemia in diabetic rats.

Journal: Growth factors (Chur, Switzerland)

Published: August 25, 2017

Showing 1-12 of 62

Last Updated: 09/26/2026