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

Stem cells and development, 2011-01, Vol.20 (1), p.67

2011

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

Journal of translational medicine, 2013-03, Vol.11 (1), p.78-78, Article 78

2013

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

Cell biology international, 2012-08, Vol.36 (8), p.747-753

2012

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

Journal of cellular and molecular medicine, 2011-07, Vol.15 (7), p.1515-1527

2011

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

PLoS genetics, 2018-03, Vol.14 (3), p.e1007297

2018

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Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis

Journal of translational medicine, 2012-04, Vol.10 (1), p.75-75, Article 75

2012

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Tricellulin Is a Tight-Junction Protein Necessary for Hearing

American journal of human genetics, 2006-12, Vol.79 (6), p.1040-1051

2006

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Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

American journal of human genetics, 2010-03, Vol.86 (3), p.378-388

2010

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Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

American journal of human genetics, 2009-05, Vol.84 (5), p.664-671

2009

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FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Nature communications, 2016-04, Vol.7 (1), p.10953-10953, Article 10953

2016

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Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

PloS one, 2016-11, Vol.11 (11), p.e0162620-e0162620

2016

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Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

American journal of human genetics, 2014-01, Vol.94 (1), p.144-152

2014

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Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families

Investigative ophthalmology & visual science, 2017-04, Vol.58 (4), p.2218-2238

2017

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A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa

American journal of human genetics, 2010-05, Vol.86 (5), p.805-812

2010

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

PLoS genetics, 2013-09, Vol.9 (9), p.e1003774-e1003774

2013

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Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

PloS one, 2016-12, Vol.11 (12), p.e0167562

2016

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

Stem Cells International, 2015-01, Vol.2015, p.747245-12

2015

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

Cell biology international, 2016-05, Vol.40 (5), p.579-588

2016

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Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

PloS one, 2017-03, Vol.12 (3), p.e0173719-e0173719

2017

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

Journal of translational medicine, 2012-12, Vol.10 (1), p.243-243, Article 243

2012

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

Inflammation research, 2013-08, Vol.62 (8), p.781-789

2013

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

Cell and tissue research, 2013-03, Vol.351 (3), p.433-443

2013

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Phenotypic Variability Associated with the D226N Allele of IMPDH1

Ophthalmology (Rochester, Minn.), 2015-02, Vol.122 (2), p.429-431

2015

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A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness

American journal of human genetics, 2010-10, Vol.87 (4), p.523-531

2010

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Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss

Human genetics, 2015-04, Vol.134 (4), p.423-437

2015

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

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

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

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

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

Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis

Tricellulin Is a Tight-Junction Protein Necessary for Hearing

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families

A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa

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

Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

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

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

Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

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

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

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

Phenotypic Variability Associated with the D226N Allele of IMPDH1

A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss

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