Found: 40
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Adipose stem cells differentiated chondrocytes regenerate damaged cartilage in rat model of osteoarthritis.
- Published in:
- Cell Biology International, 2016, v. 40, n. 5, p. 579, doi. 10.1002/cbin.10596
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- Publication type:
- Article
Diazoxide preconditioning of endothelial progenitor cells improves their ability to repair the infarcted myocardium.
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- Cell Biology International, 2015, v. 39, n. 11, p. 1251, doi. 10.1002/cbin.10498
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- Publication type:
- Article
Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities.
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- Cell Biology International, 2012, v. 36, n. 8, p. 747, doi. 10.1042/CBI20110183
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- Publication type:
- Article
IGF-1 and G-CSF complement each other in BMSC migration towards infarcted myocardium in a novel in vitro model
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- Cell Biology International, 2009, v. 33, n. 6, p. 650, doi. 10.1016/j.cellbi.2009.03.002
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- Publication type:
- Article
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.
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- Journal of Human Genetics, 2013, v. 58, n. 9, p. 641, doi. 10.1038/jhg.2013.85
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- Article
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.
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- Journal of Human Genetics, 2013, v. 58, n. 2, p. 102, doi. 10.1038/jhg.2012.143
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- Publication type:
- Article
USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.
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- Journal of Human Genetics, 2012, v. 57, n. 10, p. 633, doi. 10.1038/jhg.2012.79
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- Publication type:
- Article
Molecular and clinical studies of X-linked deafness among Pakistani families.
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- Journal of Human Genetics, 2011, v. 56, n. 10, p. 752, doi. 10.1038/jhg.2011.89
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- Article
Molecular and clinical studies of X-linked deafness among Pakistani families.
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- Journal of Human Genetics, 2011, v. 56, n. 7, p. 534, doi. 10.1038/jhg.2011.55
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- Publication type:
- Article
Preconditioning diabetic mesenchymal stem cells with myogenic medium increases their ability to repair diabetic heart.
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- Stem Cell Research & Therapy, 2013, v. 4, n. 3, p. 1, doi. 10.1186/scrt207
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- Publication type:
- Article
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse.
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- PLoS Genetics, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pgen.1007297
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- Publication type:
- Article
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
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- Human Genetics, 2007, v. 122, n. 5, p. 445, doi. 10.1007/s00439-007-0418-z
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- Publication type:
- Article
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3.
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- Human Genetics, 2007, v. 120, n. 6, p. 789, doi. 10.1007/s00439-006-0275-1
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- Publication type:
- Article
A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype.
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- European Journal of Human Genetics, 2013, v. 21, n. 8, p. 844, doi. 10.1038/ejhg.2012.257
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- Publication type:
- Article
Mesenchymal stem cells conditioned with glucose depletion augments their ability to repair-infarcted myocardium.
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- Journal of Cellular & Molecular Medicine, 2012, v. 16, n. 10, p. 2518, doi. 10.1111/j.1582-4934.2012.01568.x
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- Publication type:
- Article
Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice.
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- Journal of Cellular & Molecular Medicine, 2011, v. 15, n. 7, p. 1515, doi. 10.1111/j.1582-4934.2009.00998.x
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- Publication type:
- Article
Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases.
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- Molecular Vision, 2016, v. 22, p. 1
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- Publication type:
- Article
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases.
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- Molecular Vision, 2016, v. 22, p. 1
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- Publication type:
- Article
FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.
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- Nature Communications, 2016, v. 7, n. 4, p. 1, doi. 10.1038/ncomms10953
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- Publication type:
- Article
In vitro preconditioning of insulin-producing cells with growth factors improves their survival and ability to release insulin.
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- Journal of Biosciences, 2018, v. 43, n. 4, p. 649, doi. 10.1007/s12038-018-9796-8
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- Publication type:
- Article
In-vitro model systems to study Hepatitis C Virus.
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- Genetic Vaccines & Therapy, 2011, v. 9, n. 1, p. 7, doi. 10.1186/1479-0556-9-7
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- Publication type:
- Article
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
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- PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167562
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- Publication type:
- Article
Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts.
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- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0162620
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- Publication type:
- Article
Stromal cell derived factor-1alpha protects stem cell derived insulin-producing cells from glucotoxicity under high glucose conditions in-vitro and ameliorates drug induced diabetes in rats.
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- Journal of Translational Medicine, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1479-5876-11-115
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- Publication type:
- Article
Mesenchymal stem cells and Interleukin-6 attenuate liver fibrosis in mice.
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- Journal of Translational Medicine, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1479-5876-11-78
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- Publication type:
- Article
Stromal cell derived factor-1alpha protects stem cell derived insulin-producing cells from glucotoxicity under high glucose conditions in-vitro and ameliorates drug induced diabetes in rats.
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- 2013
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- Publication type:
- journal article
Mesenchymal stem cells and Interleukin-6 attenuate liver fibrosis in mice.
- Published in:
- 2013
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- Publication type:
- journal article
Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment.
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- Journal of Translational Medicine, 2012, v. 10, n. 1, p. 243, doi. 10.1186/1479-5876-10-243
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- Publication type:
- Article
Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis.
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- Journal of Translational Medicine, 2012, v. 10, n. 1, p. 75, doi. 10.1186/1479-5876-10-75
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- Publication type:
- Article
Human neonatal stem cell‐derived skin substitute improves healing of severe burn wounds in a rat model.
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- Cell Biology International, 2019, v. 43, n. 2, p. 147, doi. 10.1002/cbin.11072
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- Publication type:
- Article
In Vitro Differentiation Potential of Human Placenta Derived Cells into Skin Cells.
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- Stem Cells International, 2015, v. 2015, p. 1, doi. 10.1155/2015/841062
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- Publication type:
- Article
Mesenchymal Stem Cells Pretreated with HGF and FGF4 Can Reduce Liver Fibrosis in Mice.
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- Stem Cells International, 2015, v. 2015, p. 1, doi. 10.1155/2015/747245
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- Publication type:
- Article
An Alteration in ELMOD3, an Arl2 GTPase-Activating Protein, Is Associated with Hearing Impairment in Humans.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 9, p. 1, doi. 10.1371/journal.pgen.1003774
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- Publication type:
- Article
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
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- Human Mutation, 2019, v. 40, n. 1, p. 53, doi. 10.1002/humu.23666
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- Publication type:
- Article
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
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- Human Mutation, 2016, v. 37, n. 10, p. 991, doi. 10.1002/humu.23042
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- Article
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
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- Human Mutation, 2008, v. 29, n. 4, p. 502, doi. 10.1002/humu.20677
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- Publication type:
- Article
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus.
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- Human Mutation, 2007, v. 28, n. 5, p. 417, doi. 10.1002/humu.20469
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- Publication type:
- Article
Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
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- 2017
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- Publication type:
- Correction Notice
Genetic Analysis through OtoSeq of Pakistani Families Segregating Prelingual Hearing Loss.
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- Otolaryngology-Head & Neck Surgery, 2013, v. 149, n. 3, p. 478, doi. 10.1177/0194599813493075
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- Publication type:
- Article
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.
- Published in:
- BMC Medical Genetics, 2011, v. 12, n. 1, p. 21, doi. 10.1186/1471-2350-12-21
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- Publication type:
- Article