Pages that link to "Q24680145"
Jump to navigation
Jump to search
The following pages link to The expression of mutant epidermal keratin cDNAs transfected in simple epithelial and squamous cell carcinoma lines (Q24680145):
Displaying 50 items.
- Demonstration of the pathogenic effect of point mutated keratin 9 in vivo (Q22009458) (← links)
- Dissection of protein linkage between keratins and pinin, a protein with dual location at desmosome-intermediate filament complex and in the nucleus (Q22254091) (← links)
- The nonhelical tail domain of keratin 14 promotes filament bundling and enhances the mechanical properties of keratin intermediate filaments in vitro (Q24291939) (← links)
- Molecular characterization of the body site-specific human epidermal cytokeratin 9: cDNA cloning, amino acid sequence, and tissue specificity of gene expression (Q24305039) (← links)
- A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein (Q24306295) (← links)
- Keratin 16 and keratin 17 mutations cause pachyonychia congenita (Q24307427) (← links)
- The human gene encoding cytokeratin 20 and its expression during fetal development and in gastrointestinal carcinomas (Q24312239) (← links)
- A splice site mutation in the gene of the human type I hair keratin hHa1 results in the expression of a tailless keratin isoform (Q24314762) (← links)
- Mouse differentiation-specific keratins 1 and 10 require a preexisting keratin scaffold to form a filament network (Q24337663) (← links)
- Isolation, sequence, and differential expression of a human K7 gene in simple epithelial cells (Q24338645) (← links)
- Extensive size polymorphism of the human keratin 10 chain resides in the C-terminal V2 subdomain due to variable numbers and sizes of glycine loops (Q24563316) (← links)
- Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity (Q24606047) (← links)
- Posttranslational regulation of keratins: degradation of mouse and human keratins 18 and 8 (Q24634036) (← links)
- Filensin: a new vimentin-binding, polymerization-competent, and membrane-associated protein of the lens fiber cell (Q24644180) (← links)
- Making a connection: direct binding between keratin intermediate filaments and desmosomal proteins (Q24651318) (← links)
- Breaking the connection: displacement of the desmosomal plaque protein desmoplakin from cell-cell interfaces disrupts anchorage of intermediate filament bundles and alters intercellular junction assembly (Q24671724) (← links)
- Insights into the dynamic properties of keratin intermediate filaments in living epithelial cells (Q24681167) (← links)
- Defining keratin protein function in skin epithelia: epidermolysis bullosa simplex and its aftermath (Q26852211) (← links)
- A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering (Q28186252) (← links)
- Network antibodies identify nuclear lamin B as a physiological attachment site for peripherin intermediate filaments (Q28262899) (← links)
- Mutations in a keratin 6 isomer (K6c) cause a type of focal palmoplantar keratoderma (Q28270725) (← links)
- PKN associates and phosphorylates the head-rod domain of neurofilament protein (Q28277817) (← links)
- Functional analysis of desmoplakin domains: specification of the interaction with keratin versus vimentin intermediate filament networks (Q28298571) (← links)
- Assembly properties of dominant and recessive mutations in the small mouse neurofilament (NF-L) subunit (Q28512783) (← links)
- Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival (Q28592841) (← links)
- Expression of NF-L and NF-M in fibroblasts reveals coassembly of neurofilament and vimentin subunits (Q28592927) (← links)
- Discovery of keratin function and role in genetic diseases: the year that 1991 was. (Q30355097) (← links)
- Peripherin expression in hippocampal neurons induced by muscle soluble factor(s). (Q30442260) (← links)
- Dynamic relationship of focal contacts and hemidesmosome protein complexes in live cells (Q30494806) (← links)
- Identification of novel principles of keratin filament network turnover in living cells (Q30579430) (← links)
- Steady state dynamics of intermediate filament networks (Q30798792) (← links)
- Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis (Q30990411) (← links)
- cDNA cloning, expression, and assembly characteristics of mouse keratin 16. (Q31971352) (← links)
- Some neural intermediate filaments contain both peripherin and the neurofilament proteins (Q33303511) (← links)
- The use of biosensor technology for the engineering of antibodies and enzymes (Q33682947) (← links)
- Dynamic aspects of intermediate filament networks in BHK-21 cells (Q33831655) (← links)
- Tissue-specific and differentiation-specific expression of a human K14 keratin gene in transgenic mice (Q33840379) (← links)
- Defining the properties of the nonhelical tail domain in type II keratin 5: insight from a bullous disease-causing mutation (Q33914435) (← links)
- Dominant maternal-effect mutations causing embryonic lethality in Caenorhabditis elegans (Q33956624) (← links)
- Sorting out IF networks: consequences of domain swapping on IF recognition and assembly (Q34000890) (← links)
- The 'ins' and 'outs' of intermediate filament organization. (Q34040282) (← links)
- The Molecular Genetics of Keratin Disorders (Q34189864) (← links)
- The Two Size Alleles of Human Keratin 1 Are Due to a Deletion in the Glycine-Rich Carboxyl-Terminal V2 Subdomain (Q34207557) (← links)
- Molecular interactions in paracrystals of a fragment corresponding to the alpha-helical coiled-coil rod portion of glial fibrillary acidic protein: evidence for an antiparallel packing of molecules and polymorphism related to intermediate filament s (Q34535291) (← links)
- Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses (Q34591440) (← links)
- The importance of intramolecular ion pairing in intermediate filaments (Q34805039) (← links)
- Renal cells express different forms of vimentin: the independent expression alteration of these forms is important in cell resistance to osmotic stress and apoptosis (Q34847839) (← links)
- Truncated desmin in PtK2 cells induces desmin-vimentin-cytokeratin coprecipitation, involution of intermediate filament networks, and nuclear fragmentation: a model for many degenerative diseases (Q35118655) (← links)
- The molecular biology of intermediate filament proteins (Q35317711) (← links)
- The role of protein domains in the assembly process of intermediate filaments (Q35420432) (← links)