Shaheen N Khan

Shaheen N Khan

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Shaheen N Khan

Publications by authors named "Shaheen N Khan"

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

Cell Biol Int 2019 Feb;43(2):147-157

National Center of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1002/cbin.11072DOI Listing
February 2019

Human amniotic membrane as differentiating matrix for in vitro chondrogenesis.

Regen Med 2018 10 9;13(7):821-832. Epub 2018 Oct 9.

Centre of Excellence in Molecular Biology, 87 West Canal Bank Road, Thokar Niazbaig Lahore, Punjab, 53700 Pakistan.

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https://www.futuremedicine.com/doi/10.2217/rme-2018-0017
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http://dx.doi.org/10.2217/rme-2018-0017DOI Listing
October 2018

Whole genome sequencing data for two individuals of Pakistani descent.

Sci Data 2018 09 11;5:180174. Epub 2018 Sep 11.

The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

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http://www.nature.com/articles/sdata2018174
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http://dx.doi.org/10.1038/sdata.2018.174DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137601PMC
September 2018

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

J Biosci 2018 Sep;43(4):649-659

National Centre of Excellence in Molecular Biology, University of Punjab, 87-West Canal Bank Road, Lahore, Pakistan.

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September 2018

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

J Med Genet 2018 07 23;55(7):479-488. Epub 2018 Mar 23.

Department of Otorhinolaryngology Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1136/jmedgenet-2017-105221DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232856PMC
July 2018

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

PLoS Genet 2018 03 28;14(3):e1007297. Epub 2018 Mar 28.

Laboratory of Molecular Genetics, Department of Otorhinolaryngology-Head & Neck Surgery, School of Medicine University of Maryland, Baltimore, MD, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1007297DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891075PMC
March 2018

Protective role of vitamin E preconditioning of human dermal fibroblasts against thermal stress in vitro.

Life Sci 2017 Sep 3;184:1-9. Epub 2017 Jul 3.

National Centre of Excellence in Molecular Biology, 87-West Canal Bank Road, University of the Punjab, Lahore, Pakistan; Allama Iqbal Medical College, University of Health Sciences, Lahore, Pakistan; Shaheed Zulfiqar Ali Bhutto Medical University (SZABMU), Islamabad, Pakistan. Electronic address:

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http://dx.doi.org/10.1016/j.lfs.2017.07.002DOI Listing
September 2017

Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosa.

Hum Genome Var 2016 17;3:16036. Epub 2016 Nov 17.

The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

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http://dx.doi.org/10.1038/hgv.2016.36DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112436PMC
November 2016

Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.

Hum Mutat 2016 10 21;37(10):991-1003. Epub 2016 Aug 21.

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, 20892.

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http://dx.doi.org/10.1002/humu.23042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5021573PMC
October 2016

Adipose stem cells differentiated chondrocytes regenerate damaged cartilage in rat model of osteoarthritis.

Cell Biol Int 2016 May 21;40(5):579-88. Epub 2016 Mar 21.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1002/cbin.10596DOI Listing
May 2016

N-Acetyl cysteine protects diabetic mouse derived mesenchymal stem cells from hydrogen-peroxide-induced injury: A novel hypothesis for autologous stem cell transplantation.

J Chin Med Assoc 2016 Mar 26;79(3):122-9. Epub 2016 Feb 26.

The University of Lahore, Defence Road Campus, Lahore, Pakistan; National Center of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan; Allama Iqbal Medical College/Jinnah Hospital Complex, University of Health Sciences, Lahore, Pakistan.

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http://dx.doi.org/10.1016/j.jcma.2015.09.005DOI Listing
March 2016

Diazoxide preconditioning of endothelial progenitor cells improves their ability to repair the infarcted myocardium.

Cell Biol Int 2015 Nov 7;39(11):1251-63. Epub 2015 Jul 7.

National Centre of Excellence in Molecular Biology, 87-West Canal Bank Road, University of Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1002/cbin.10498DOI Listing
November 2015

In Vitro Differentiation Potential of Human Placenta Derived Cells into Skin Cells.

Stem Cells Int 2015 1;2015:841062. Epub 2015 Jul 1.

National Center of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan ; Allama Iqbal Medical College, Lahore, Pakistan.

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http://www.hindawi.com/journals/sci/2015/841062/
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http://dx.doi.org/10.1155/2015/841062DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4502554PMC
August 2015

Phenotypic variability associated with the D226N allele of IMPDH1.

Ophthalmology 2015 Feb 13;122(2):429-31. Epub 2014 Nov 13.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address:

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http://dx.doi.org/10.1016/j.ophtha.2014.07.057DOI Listing
February 2015

Mesenchymal Stem Cells Pretreated with HGF and FGF4 Can Reduce Liver Fibrosis in Mice.

Stem Cells Int 2015 20;2015:747245. Epub 2015 Jan 20.

National Centre of Excellence in Molecular Biology, 87 West Canal Bank Road, Thokar Niaz Baig, Lahore 53700, Pakistan.

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http://downloads.hindawi.com/journals/sci/2015/747245.pdf
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http://www.hindawi.com/journals/sci/2015/747245/
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http://dx.doi.org/10.1155/2015/747245DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320872PMC
February 2015

An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humans.

PLoS Genet 2013 5;9(9):e1003774. Epub 2013 Sep 5.

Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1003774DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764207PMC
March 2014

Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy.

Mol Vis 2013 19;19:1554-64. Epub 2013 Jul 19.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716412PMC
September 2013

Vitamin E protects chondrocytes against hydrogen peroxide-induced oxidative stress in vitro.

Inflamm Res 2013 Aug 31;62(8):781-9. Epub 2013 May 31.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Lahore, 53700, Pakistan.

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http://dx.doi.org/10.1007/s00011-013-0635-yDOI Listing
August 2013

Lovastatin protects chondrocytes derived from Wharton's jelly of human cord against hydrogen-peroxide-induced in vitro injury.

Cell Tissue Res 2013 Mar 28;351(3):433-43. Epub 2012 Dec 28.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Lahore, Pakistan.

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http://dx.doi.org/10.1007/s00441-012-1540-3DOI Listing
March 2013

Mesenchymal stem cells and Interleukin-6 attenuate liver fibrosis in mice.

J Transl Med 2013 Mar 26;11:78. Epub 2013 Mar 26.

National Center of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Lahore, Pakistan.

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http://dx.doi.org/10.1186/1479-5876-11-78DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636128PMC
March 2013

Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment.

J Transl Med 2012 Dec 5;10:243. Epub 2012 Dec 5.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1186/1479-5876-10-243DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543338PMC
December 2012

USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.

J Hum Genet 2012 Oct 21;57(10):633-7. Epub 2012 Jun 21.

Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

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http://dx.doi.org/10.1038/jhg.2012.79DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596105PMC
October 2012

Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities.

Cell Biol Int 2012 Aug;36(8):747-53

National Center of Excellence in Molecular Biology, 87 West Canal Bank Road, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1042/CBI20110183DOI Listing
August 2012

Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis.

J Transl Med 2012 Apr 25;10:75. Epub 2012 Apr 25.

National Center of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1186/1479-5876-10-75DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419634PMC
April 2012

Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice.

J Cell Mol Med 2011 Jul 11;15(7):1515-27. Epub 2009 Dec 11.

National Center of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Lahore, Pakistan.

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http://dx.doi.org/10.1111/j.1582-4934.2009.00998.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823196PMC
July 2011

Molecular and clinical studies of X-linked deafness among Pakistani families.

J Hum Genet 2011 Jul 2;56(7):534-40. Epub 2011 Jun 2.

National Center of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1038/jhg.2011.55DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143270PMC
July 2011

In-vitro model systems to study Hepatitis C Virus.

Genet Vaccines Ther 2011 Apr 6;9. Epub 2011 Apr 6.

Division of Molecular Medicine, National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1186/1479-0556-9-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3083322PMC
April 2011

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.

BMC Med Genet 2011 Feb 9;12:21. Epub 2011 Feb 9.

Laboratory of Molecular Genetics, Division of Pediatric Otolaryngology Head & Neck Surgery, Cincinnati Children's Hospital Research Foundation, and University of Cincinnati, College of Medicine, Cincinnati, OH, USA.

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http://dx.doi.org/10.1186/1471-2350-12-21DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042908PMC
February 2011

Growth factor preconditioning increases the function of diabetes-impaired mesenchymal stem cells.

Stem Cells Dev 2011 Jan 12;20(1):67-75. Epub 2010 Oct 12.

National Center of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1089/scd.2009.0397DOI Listing
January 2011

Enhanced hepatic differentiation of mesenchymal stem cells after pretreatment with injured liver tissue.

Differentiation 2011 Jan 12;81(1):42-8. Epub 2010 Oct 12.

National Center of Excellence in Molecular Biology, 87-West Canal Bank Road, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1016/j.diff.2010.08.005DOI Listing
January 2011

Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

Am J Hum Genet 2011 Jan 23;88(1):19-29. Epub 2010 Dec 23.

Laboratory of Molecular Genetics, Division of Pediatric Otolaryngology Head & Neck Surgery, Cincinnati Children's Hospital Research Foundation, and the Department of Otolaryngology, College of Medicine, University of Cincinnati, OH, 45229 USA.

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http://dx.doi.org/10.1016/j.ajhg.2010.11.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014371PMC
January 2011

Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family.

Br J Ophthalmol 2010 Aug 10;94(8):1094-9. Epub 2010 Jun 10.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87 West Canal Bank Road, Lahore 53700, Pakistan.

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http://dx.doi.org/10.1136/bjo.2009.171892DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393880PMC
August 2010

Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.

Am J Hum Genet 2010 Mar 18;86(3):378-88. Epub 2010 Feb 18.

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.

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http://dx.doi.org/10.1016/j.ajhg.2010.01.030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833391PMC
March 2010

Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family.

Mol Vis 2010 Mar 24;16:511-7. Epub 2010 Mar 24.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846848PMC
March 2010

A new locus for autosomal recessive congenital cataract identified in a Pakistani family.

Mol Vis 2010 Feb 16;16:240-5. Epub 2010 Feb 16.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822550PMC
February 2010

IGF-1 and G-CSF complement each other in BMSC migration towards infarcted myocardium in a novel in vitro model.

Cell Biol Int 2009 Jun 13;33(6):650-7. Epub 2009 Mar 13.

National Center of Excellence in Molecular Biology (CEMB), University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1016/j.cellbi.2009.03.002DOI Listing
June 2009

Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.

Mol Vis 2008 3;14:2002-9. Epub 2008 Nov 3.

National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2579935PMC
March 2009

Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.

Hum Mutat 2008 Apr;29(4):502-11

Section on Human Genetics, Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Maryland 20850, USA.

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http://dx.doi.org/10.1002/humu.20677DOI Listing
April 2008

The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.

Hum Genet 2007 Dec 10;122(5):445-50. Epub 2007 Aug 10.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Thokar Niaz Baig, Lahore, 53700, Pakistan.

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http://dx.doi.org/10.1007/s00439-007-0418-zDOI Listing
December 2007

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

Hum Genet 2007 Feb 26;120(6):789-93. Epub 2006 Oct 26.

National Center of Excellence in Molecular Biology, University of Punjab, 87-West Canal Bank Road, Thokar Niaz Baig, Lahore, Pakistan.

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http://dx.doi.org/10.1007/s00439-006-0275-1DOI Listing
February 2007

Tricellulin is a tight-junction protein necessary for hearing.

Am J Hum Genet 2006 Dec 31;79(6):1040-51. Epub 2006 Oct 31.

Section on Human Genetics, Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.

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http://dx.doi.org/10.1086/510022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1698716PMC
December 2006

Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.

Am J Hum Genet 2006 Jan 21;78(1):137-43. Epub 2005 Nov 21.

Section on Human Genetics, Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health (NIH), Rockville, MD 20850, USA.

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http://dx.doi.org/10.1086/499164DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1380211PMC
January 2006

DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1.

Hum Genet 2005 Apr 12;116(5):407-12. Epub 2005 Feb 12.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Thokar Niaz Baig, Lahore, 53700 Pakistan.

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http://dx.doi.org/10.1007/s00439-004-1247-yDOI Listing
April 2005

A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.

Hum Genet 2005 Jan 6;116(1-2):17-22. Epub 2004 Nov 6.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Thokar Niaz Baig, Lahore 53700, Pakistan.

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http://dx.doi.org/10.1007/s00439-004-1205-8DOI Listing
January 2005

Molecular characterization of alpha-thalassemia in Pakistan.

Hemoglobin 2003 Aug;27(3):161-6

Centre for Applied Molecular Biology, University of the Punjab, Thokar Niaz Baig, Lahore, Pakistan.

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http://dx.doi.org/10.1081/hem-120023379DOI Listing
August 2003

Mutations of MYO6 are associated with recessive deafness, DFNB37.

Am J Hum Genet 2003 May 8;72(5):1315-22. Epub 2003 Apr 8.

Section on Human Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1180285PMC
http://dx.doi.org/10.1086/375122DOI Listing
May 2003