368 results on '"Riazuddin, Sheikh"'
Search Results
2. Adipose Tissue and Umbilical Cord Tissue: Potential Sources of Mesenchymal Stem Cells for Liver Fibrosis Treatment
3. Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.
4. Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F
5. Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness.
6. Zinc oxide loaded chitosan-elastin-sodium alginate nanocomposite gel using freeze gelation for enhanced adipose stem cell proliferation and antibacterial properties
7. Priming with caffeic acid enhances the potential and survival ability of human adipose-derived stem cells to counteract hypoxia
8. Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families
9. Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma.
10. Whole genome sequencing data of multiple individuals of Pakistani descent
11. Hydrogel patch with pretreated stem cells accelerates wound closure in diabetic rats
12. Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
13. A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts
14. New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder
15. Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disability
16. Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa.
17. A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred.
18. Standardization of diethylnitrosamine-induced hepatocellular carcinoma rat model with time based molecular assessment
19. A mutation in IFT43 causes non-syndromic recessive retinal degeneration
20. Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
21. Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani FamiliesPakistani RP Study
22. A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes
23. Curcumin preconditioned human adipose derived stem cells co-transplanted with platelet rich plasma improve wound healing in diabetic rats
24. Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features
25. CIB2 regulates mTORC1 signaling and is essential for autophagy and visual function
26. FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.
27. Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases.
28. Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosa
29. Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases.
30. Cassia Angustifolia Primed ASCs Accelerate Burn Wound Healing by Modulation of Inflammatory Response
31. Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice
32. Sarcococca saligna fabricated gold nanoparticles alleviated in vitro oxidative stress and inflammation in human adipose‐derived stem cells
33. Corrigendum to “Priming of adipose-derived stem cells with curcumin prior to cryopreservation preserves their functional potency: Towards an ‘Off-the-shelf’ therapy for burns” [Cryobiology 110 (2023) 69–78]
34. Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome.
35. Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
36. Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families.
37. Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness.
38. Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome Sequencing.
39. Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia
40. A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI)
41. Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two Pedigrees
42. Whole-Exome Sequencing Identifies Novel Variants that Co-segregates with Autosomal Recessive Retinal Degeneration in a Pakistani Pedigree
43. Anti-hepatitis C virus activity and synergistic effect of Nymphaea alba extracts and bioactive constituents in liver infected cells
44. Genetic Epidemiology of Congenital Cataracts and Autosomal Recessive Retinal Degenerations in Pakistan
45. In vitro preconditioning of insulin-producing cells with growth factors improves their survival and ability to release insulin
46. Protective role of vitamin E preconditioning of human dermal fibroblasts against thermal stress in vitro
47. Variants ofLRP2, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy
48. Priming of adipose-derived stem cells with curcumin prior to cryopreservation preserves their functional potency: Towards an ‘Off-the-shelf’ therapy for burns
49. Dual AAV-based PCDH15gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F
50. 7. Cell therapy for liver regeneration
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