Pages that link to "Q34262977"

The following pages link to A mutation in the gene for type III procollagen (COL3A1) in a family with aortic aneurysms (Q34262977):

Displaying 50 items.

• Genetic causes of aortic aneurysms. Unlearning at least part of what the textbooks say (Q24630440) ‎ (← links)
• Haploinsufficiency of the murine Col3a1 locus causes aortic dissection: a novel model of the vascular type of Ehlers-Danlos syndrome (Q28507740) ‎ (← links)
• G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination (Q28512264) ‎ (← links)
• Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development (Q28588213) ‎ (← links)
• Ehlers-Danlos syndrome type IV with a unique point mutation in COL3A1 and familial phenotype of myocardial infarction without organic coronary stenosis (Q31902090) ‎ (← links)
• Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IV (Q33594086) ‎ (← links)
• The substitution of glycine 661 by arginine in type III collagen produces mutant molecules with different thermal stabilities and causes Ehlers-Danlos syndrome type IV (Q33595705) ‎ (← links)
• Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV (Q33597264) ‎ (← links)
• Etiologic factors of acute aortic dissection in children and young adults (Q33851335) ‎ (← links)
• Hydrolyzed eggshell membrane immobilized on phosphorylcholine polymer supplies extracellular matrix environment for human dermal fibroblasts. (Q33906757) ‎ (← links)
• Loss of Col3a1, the gene for Ehlers-Danlos syndrome type IV, results in neocortical dyslamination (Q34123887) ‎ (← links)
• GPR56 and the developing cerebral cortex: cells, matrix, and neuronal migration (Q34301363) ‎ (← links)
• Genes and abdominal aortic aneurysm (Q34683905) ‎ (← links)
• Sequencing of cDNA from 50 unrelated patients reveals that mutations in the triple-helical domain of type III procollagen are an infrequent cause of aortic aneurysms (Q34731356) ‎ (← links)
• Parental somatic and germ-line mosaicism for a multiexon deletion with unusual endpoints in a type III collagen (COL3A1) allele produces Ehlers-Danlos syndrome type IV in the heterozygous offspring (Q35194635) ‎ (← links)
• Substitution of aspartate for glycine 1018 in the type III procollagen (COL3A1) gene causes type IV Ehlers-Danlos syndrome: the mutated allele is present in most blood leukocytes of the asymptomatic and mosaic mother. (Q35195812) ‎ (← links)
• Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus (Q35196278) ‎ (← links)
• Aortic dissection and aortic aneurysm surgery: Clinical observations, experimental investigations, and statistical analyses part II (Q35197160) ‎ (← links)
• Small leucine-rich proteoglycans exhibit unique spatiotemporal expression profiles during cardiac valve development (Q35566074) ‎ (← links)
• Novel insights into the function and dynamics of extracellular matrix in liver fibrosis (Q35622533) ‎ (← links)
• A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection. (Q35643001) ‎ (← links)
• Decreased vascular smooth muscle cell density in medial degeneration of human abdominal aortic aneurysms. (Q35763570) ‎ (← links)
• The pivotal role of matrix metalloproteinases in the development of human abdominal aortic aneurysms. (Q35763818) ‎ (← links)
• Induction of aneurysms in the rat by a stenosing cotton ligature around the inter-renal aorta. (Q36028219) ‎ (← links)
• Pathogenesis of Acquired Aneurysms of the Abdominal Aorta (Q36233174) ‎ (← links)
• Extracellular matrix remodeling: the common denominator in connective tissue diseases. Possibilities for evaluation and current understanding of the matrix as more than a passive architecture, but a key player in tissue failure (Q36672445) ‎ (← links)
• Surgery insight: the dilated ascending aorta--indications for surgical intervention (Q36830720) ‎ (← links)
• Mutations in Collagen Genes as a Cause of Rare and Perhaps Common Diseases of Connective Tissue (Q37043691) ‎ (← links)
• Genetics of ischaemic stroke; single gene disorders (Q37244585) ‎ (← links)
• Valve replacement options in the setting of an ascending aortic aneurysm. (Q37572800) ‎ (← links)
• The importance of extracellular matrix for cell function and in vivo likeness. (Q38321523) ‎ (← links)
• Clinical recognition of aortic dissection. (Q40485851) ‎ (← links)
• The perivascular connective matrix (Q40616929) ‎ (← links)
• Collagens and their abnormalities in a wide spectrum of diseases (Q40853815) ‎ (← links)
• Molecular genetics of Alport syndrome (Q40876120) ‎ (← links)
• Pathogenesis of abdominal aortic aneurysms--cellular and biochemical mechanisms (Q41288569) ‎ (← links)
• Basement-membrane stromal relationships: interactions between collagen fibrils and the lamina densa (Q41452411) ‎ (← links)
• Diagnosis and treatment of diseases of the aorta (Q41618136) ‎ (← links)
• Epidemiology and potential for prevention of abdominal aortic aneurysm (Q41720738) ‎ (← links)
• Abnormalities in the Biosynthesis of Type III Procollagen in Cultured Skin Fibroblasts from Two Patients with Multiple Aneurysms (Q41972017) ‎ (← links)
• A functional variant of the collagen type III alpha1 gene modify risk of sporadic intracranial aneurysms (Q43500373) ‎ (← links)
• Type III collagen mutations cause fragile cerebral arteries (Q47574480) ‎ (← links)
• Thoracic aortic rupture and aortopulmonary fistulation in the Friesian horse: histomorphologic characterization (Q49074922) ‎ (← links)
• Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. (Q52345694) ‎ (← links)
• Unrestricted usage of immunoglobulin heavy chain genes in B cells infiltrating the wall of atherosclerotic abdominal aortic aneurysms (Q56891639) ‎ (← links)
• Genetic variants of collagen III and abdominal aortic aneurysm (Q56891862) ‎ (← links)
• A novel COL3A1 gene mutation in patient with aortic dissected aneurysm and cervical artery dissections (Q57577872) ‎ (← links)
• Temperature sensitivity of aberrant RNA splicing with a mutation in theG+5 position of intron 37 of the gene for type III procollagen from a patient with Ehlers-Danlos syndrome type IV (Q57784105) ‎ (← links)
• A 15 base-pair AT-rich variable number tandem repeat in the type III procollagen gene (COL3A1) as an informative marker for 2q31-2q32.3 (Q57784115) ‎ (← links)
• Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases. (Q65950306) ‎ (← links)