232 results on '"Khan, Shaheen N."'
Search Results
2. Protective role of vitamin E preconditioning of human dermal fibroblasts against thermal stress in vitro
3. N-Acetyl cysteine protects diabetic mouse derived mesenchymal stem cells from hydrogen-peroxide-induced injury: A novel hypothesis for autologous stem cell transplantation
4. Diazoxide preconditioning of endothelial progenitor cells from streptozotocin-induced type 1 diabetic rats improves their ability to repair diabetic cardiomyopathy
5. Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
6. Vitamin E protects chondrocytes against hydrogen peroxide-induced oxidative stress in vitro
7. Lovastatin protects chondrocytes derived from Wharton’s jelly of human cord against hydrogen-peroxide-induced in vitro injury
8. Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48
9. Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p
10. A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness
11. Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family
12. A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosa
13. Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79
14. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3
15. Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3
16. DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1
17. A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1
18. Tricellulin is a tight-junction protein necessary for hearing
19. Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
20. Mutations of MYO6 are associated with recessive deafness, DFNB37. (Report)
21. Mesenchymal stem cells conditioned with glucose depletion augments their ability to repair-infarcted myocardium
22. Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
23. Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice
24. Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families
25. Ectopia Lentis in a Consanguineous Pakistani Family and a Novel Locus on Chromosome 8q
26. mutation Spectrum of MYO7A and Evaluation of a Novel Nonsyndromic Deafness DFNB2 Allele with Residual Function
27. Mutations of the RDXGene Cause Nonsyndromic Hearing Loss at the DFNB24 Locus
28. A New Locus for Nonsyndromic Deafness DFNB51 Maps to Chromosome 11p13-p12
29. Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment
30. Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis
31. Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
32. Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy
33. Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p
34. Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1
35. Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family
36. A new locus for autosomal recessive congenital cataract identified in a Pakistani family
37. Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma
38. Human neonatal stem cell‐derived skin substitute improves healing of severe burn wounds in a rat model.
39. Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
40. Human amniotic membrane as differentiating matrix for in vitro chondrogenesis.
41. Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.
42. Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse.
43. Serum from CCl 4 -induced acute rat injury model induces differentiation of ADSCs towards hepatic cells and reduces liver fibrosis.
44. Transplantation of stromal-derived factor 1α and basic fibroblast growth factor primed insulin-producing cells reverses hyperglycaemia in diabetic rats.
45. Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
46. Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases.
47. Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases.
48. Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts.
49. Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
50. Adipose stem cells differentiated chondrocytes regenerate damaged cartilage in rat model of osteoarthritis.
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