899 results on '"Riazuddin, Sheikh"'
Search Results
102. DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1
103. A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1
104. Tricellulin is a tight-junction protein necessary for hearing
105. Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
106. Field evaluation and risk assessment of transgenic indica basmati rice
107. Efficacy of intravenous infusions of UC-derived MSCs for the treatment of COVID-19: A structured summary of a phase II double blinded, randomized controlled clinical trial
108. Genomewide significant linkage to stuttering on chromosome 12
109. CIB2 regulates autophagy via Rheb-mTORC1 signaling axis
110. Homozygous and heterozygous disruptions of ANK3
111. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC
112. Mutations of MYO6 are associated with recessive deafness, DFNB37. (Report)
113. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome
114. Mesenchymal stem cells conditioned with glucose depletion augments their ability to repair-infarcted myocardium
115. Expression of multiple insecticidal genes confers broad resistance against a range of different rice pests
116. Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q
117. Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus. (Report)
118. Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33
119. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes
120. Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
121. Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice
122. Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families
123. Are variants in sex hormone metabolizing genes associated with stuttering?
124. Development of NSAID ‐loaded nano‐composite scaffolds for skin tissue engineering applications
125. Epigallocatechin-3-gallate protects Wharton's jelly derived mesenchymal stem cells against in vitro heat stress
126. RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability
127. Antioxidant pretreatment enhances umbilical cord derived stem cells survival in response to thermal stress in vitro
128. Haplotype analysis of two X-chromosome STR clusters in the Pakistani population
129. Ectopia Lentis in a Consanguineous Pakistani Family and a Novel Locus on Chromosome 8q
130. Screening, diagnosis and genetic study of breast cancer patients in Pakistan
131. Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family
132. Vitamin E preconditioning alleviates in vitro thermal stress in cultured human epidermal keratinocytes
133. Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly
134. Mutations in the Lysosomal Enzyme-Targeting Pathway and Persistent Stuttering
135. Contributors
136. Identification of Genes Causing Autosomal Recessive Retinitis Pigmentosa
137. Effect of age of seedling and phytohormones on micropropagation of indica rice (Oryza sativa L.) from Meristem Culture.
138. Studies on the expression of marker genes in chickpea
139. mutation Spectrum of MYO7A and Evaluation of a Novel Nonsyndromic Deafness DFNB2 Allele with Residual Function
140. Biallelic in-frame deletion of SOX4is associated with developmental delay, hypotonia and intellectual disability
141. Mutational Spectrum of MYO15A: The Large N-Terminal Extension of Myosin XVA Is Required for Hearing†‡
142. Mutations of the RDXGene Cause Nonsyndromic Hearing Loss at the DFNB24 Locus
143. Mutations of human TMHS cause recessively inherited non-syndromic hearing loss
144. A New Locus for Nonsyndromic Deafness DFNB51 Maps to Chromosome 11p13-p12
145. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
146. Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
147. Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment
148. Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis
149. Comparison of Anti-HCV Activity of Multiple Punica granatum Extracts and Fractions in Virus-infected Human Hepatocytes
150. Human neonatal stem cell-derived skin substitute improves healing of severe burn wounds in a rat model
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