Pages that link to "Q24323565"
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The following pages link to Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome (Q24323565):
Displaying 50 items.
- Collagen type IV alpha 1 chain (Q21130061) (← links)
- Novel COL4A1 mutations associated with HANAC syndrome: A role for the triple helical CB3[IV] domain (Q24298807) (← links)
- Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency (Q24300862) (← links)
- Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly (Q28281096) (← links)
- Cerebral microhemorrhages: mechanisms, consequences, and prevention (Q30235220) (← links)
- The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature. (Q30900506) (← links)
- Posterior fossa involvement in the diagnosis of adult-onset inherited leukoencephalopathies (Q31087193) (← links)
- New information on the genetics of stroke (Q34664010) (← links)
- Von Willebrand factor inhibits mature smooth muscle gene expression through impairment of Notch signaling (Q35005989) (← links)
- Stroke Genetics Update: 2011 (Q35602462) (← links)
- COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke (Q35671528) (← links)
- De novo and inherited mutations in COL4A2, encoding the type IV collagen α2 chain cause porencephaly (Q35671540) (← links)
- Molecular and Genetic Analyses of Collagen Type IV Mutant Mouse Models of Spontaneous Intracerebral Hemorrhage Identify Mechanisms for Stroke Prevention (Q35835524) (← links)
- COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage (Q35910809) (← links)
- Extracellular matrix and matrix receptors in blood-brain barrier formation and stroke (Q36351793) (← links)
- ER stress and basement membrane defects combine to cause glomerular and tubular renal disease resulting from Col4a1 mutations in mice (Q36627721) (← links)
- HANAC Syndrome Col4a1 Mutation Causes Neonate Glomerular Hyperpermeability and Adult Glomerulocystic Kidney Disease (Q36746050) (← links)
- Stroke-related translational research. (Q36953709) (← links)
- Advances in genetics 2010. (Q37242531) (← links)
- Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association (Q37251490) (← links)
- Basement membrane components are key players in specialized extracellular matrices (Q37739297) (← links)
- Aetiological diagnosis of ischaemic stroke in young adults (Q37802044) (← links)
- Review: molecular genetics and pathology of hereditary small vessel diseases of the brain. (Q37808273) (← links)
- Cell-matrix interactions in muscle disease (Q37944530) (← links)
- COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets (Q38036904) (← links)
- Cerebral microbleeds: a guide to detection and clinical relevance in different disease settings (Q38109534) (← links)
- The collagenopathies: review of clinical phenotypes and molecular correlations (Q38171408) (← links)
- Monogenic causes of stroke: now and the future (Q38513520) (← links)
- Genotype-phenotype correlations in pathology caused by collagen type IV alpha 1 and 2 mutations (Q38994280) (← links)
- Association of COL4A1 gene polymorphisms with cerebral palsy in a Chinese Han population (Q40989170) (← links)
- Embryo genome profiling by single-cell sequencing for successful preimplantation genetic diagnosis in a family harboring COL4A1 c.1537G>A; p.G513S mutation (Q41504446) (← links)
- Hereditary connective tissue diseases in young adult stroke: a comprehensive synthesis (Q41786268) (← links)
- Normal immunofluorescence pattern of skin basement membranes in a family with porencephaly due to COL4A1 G749S mutation (Q41926916) (← links)
- Migraine and stroke (Q41941867) (← links)
- Bidirectional encroachment of collagen into the tunica media in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (Q42013247) (← links)
- HANAC Col4a1 Mutation in Mice Leads to Skeletal Muscle Alterations due to a Primary Vascular Defect (Q42044259) (← links)
- Genetic Variations of COL4A1 gene and Intracerebral Hemorrhage risk: A case-control Study in Chinese Han Population (Q47717219) (← links)
- Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage? (Q48819583) (← links)
- Basement Membrane Defects in Genetic Kidney Diseases. (Q49455564) (← links)
- Neonatal stroke and haematuria: Answers. (Q53754759) (← links)
- Next generation sequencing uncovers a missense mutation in COL4A1 as the cause of familial retinal arteriolar tortuosity. (Q54191604) (← links)
- A novel mutation in COL4A1 gene: a possible cause of early postnatal cerebrovascular events. (Q54288815) (← links)
- Brain vascular heterogeneity: implications for disease pathogenesis and design of in vitro blood-brain barrier models. (Q55032220) (← links)
- 4-Sodium phenyl butyric acid has both efficacy and counter-indicative effects in the treatment of Col4a1 disease (Q57803015) (← links)
- Neurologic phenotypes associated with / mutations: Expanding the spectrum of disease (Q58568761) (← links)
- Cerebral Small Vessel Disease Clinical, Neuropsychological, and Radiological Phenotypes, Histopathological Correlates, and Described Genotypes: A Review (Q59103391) (← links)
- Assessment of complementarity of WGCNA and NERI results for identification of modules associated to schizophrenia spectrum disorders (Q61817393) (← links)
- Familial retinal arteriolar tortuosity and quantification of vascular tortuosity using swept-source optical coherence tomography angiography (Q64119012) (← links)
- Genetic Variations of COL4A1 Gene and Intracerebral Hemorrhage Outcome: A Cohort Study in a Chinese Han Population (Q87868482) (← links)
- Inflammatory pathways are central to posterior cerebrovascular artery remodelling prior to the onset of congenital hypertension (Q88348980) (← links)