Pages that link to "Q34136058"
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The following pages link to Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract (Q34136058):
Displaying 50 items.
- Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q (Q24295954) (← links)
- Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts (Q24299315) (← links)
- A novel HSF1-mediated death pathway that is suppressed by heat shock proteins (Q24306081) (← links)
- Association and regulation of heat shock transcription factor 4b with both extracellular signal-regulated kinase mitogen-activated protein kinase and dual-specificity tyrosine phosphatase DUSP26 (Q24313003) (← links)
- Crystallin gene mutations in Indian families with inherited pediatric cataract (Q24336750) (← links)
- CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20q (Q24337564) (← links)
- The EPHA2 gene is associated with cataracts linked to chromosome 1p (Q24658268) (← links)
- cataract 5 multiple types (Q27674895) (← links)
- Development of gene and stem cell therapy for ocular neurodegeneration (Q28081549) (← links)
- A deletion mutation in the ?A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family (Q28181790) (← links)
- Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataract (Q28260863) (← links)
- Regulation of HSF1 Function in the Heat Stress Response: Implications in Aging and Disease (Q28307651) (← links)
- Analysis of HSF4 binding regions reveals its necessity for gene regulation during development and heat shock response in mouse lenses (Q28508550) (← links)
- Developmentally dictated expression of heat shock factors: exclusive expression of HSF4 in the postnatal lens and its specific interaction with alphaB-crystallin heat shock promoter (Q28565640) (← links)
- HSF4 is required for normal cell growth and differentiation during mouse lens development (Q28584804) (← links)
- Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice (Q28589395) (← links)
- A novel mouse HSF3 has the potential to activate nonclassical heat-shock genes during heat shock (Q28594783) (← links)
- Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging (Q29614783) (← links)
- A novel HSF4 gene mutation causes autosomal-dominant cataracts in a Chinese family. (Q30360281) (← links)
- Targeted deletion of Hsf1, 2, and 4 genes in mice (Q30454339) (← links)
- A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract. (Q33323353) (← links)
- Removal of Hsf4 leads to cataract development in mice through down-regulation of gamma S-crystallin and Bfsp expression (Q33410189) (← links)
- Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening (Q33580207) (← links)
- Global gene expression analysis of lenses from different mouse strains and in the alpha3Cx46 knockout mouse (Q33608352) (← links)
- From caveman companion to medical innovator: genomic insights into the origin and evolution of domestic dogs (Q33646440) (← links)
- Whole-Genome Analysis Reveals That Active Heat Shock Factor Binding Sites Are Mostly Associated with Non-Heat Shock Genes in Drosophila melanogaster (Q33802678) (← links)
- Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3) (Q33816508) (← links)
- A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract (Q33916470) (← links)
- A missense mutation in CRYBA4 associated with congenital cataract and microcornea. (Q33933693) (← links)
- HSF4 mutation p.Arg116His found in age-related cataracts and in normal populations produces childhood lamellar cataract in transgenic mice. (Q34052848) (← links)
- Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation (Q34079601) (← links)
- A murine world without HSFs: meeting report (Q34133502) (← links)
- A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family (Q34217327) (← links)
- PDSM, a motif for phosphorylation-dependent SUMO modification (Q34248164) (← links)
- Cat-Map: putting cataract on the map (Q34248597) (← links)
- A Chinese family with progressive childhood cataracts and IVS3+1G>A CRYBA3/A1 mutations (Q34366283) (← links)
- Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations (Q34426860) (← links)
- The genetics of eye disorders in the dog (Q34495471) (← links)
- Expression of the HSF4 DNA binding domain-EGFP hybrid gene recreates early childhood lamellar cataract in transgenic mice (Q34511170) (← links)
- Regulation of the mammalian heat shock factor 1. (Q34548551) (← links)
- Autosomal recessive juvenile onset cataract associated with mutation in BFSP1. (Q34602323) (← links)
- Role of heat-shock factor 2 in cerebral cortex formation and as a regulator of p35 expression (Q34649131) (← links)
- Clinical and experimental advances in congenital and paediatric cataracts. (Q34699906) (← links)
- Rapid and cost-effective molecular diagnosis using exome sequencing of one proband with autosomal dominant congenital cataract (Q34718407) (← links)
- Molecular parameters of hyperthermia for radiosensitization (Q34990657) (← links)
- A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree (Q35024318) (← links)
- Dealing with misfolded proteins: examining the neuroprotective role of molecular chaperones in neurodegeneration. (Q35096762) (← links)
- A recurrent missense mutation in GJA3 associated with autosomal dominant cataract linked to chromosome 13q (Q35189316) (← links)
- Investigation of crystallin genes in familial cataract, and report of two disease associated mutations. (Q35591625) (← links)
- Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene (Q35592854) (← links)