نتایج جستجو برای: collagen type vi

تعداد نتایج: 1418081  

Journal: :Journal of Biological Chemistry 1989

Journal: :The Biochemical journal 1989
I A King A Tabiowo P R Fryer F M Pope

The major concanavalin A-binding component in urea/deoxycholate/mercaptoethanol extracts of pig skin was a collagenous disulphide-cross-linked glycopolypeptide with an apparent molecular mass of 150 kDa and a pI of 5.5. Antiserum against the electrophoretically purified glycopolypeptide gave strong dermal staining similar to that seen with fluorescent concanavalin A. Immunocytochemical labellin...

Journal: :Journal of clinical pathology 1993
M Shimizu K Umeda N Sugihara H Yoshio H Ino R Takeda Y Okada I Nakanishi

AIMS To investigate collagen remodelling in the interstitium of the heart in patients with diabetes. METHODS Immunohistochemical study of the biopsied myocardium using type specific anticollagen antibodies (I, III, IV, V, VI) was performed in 12 patients with non-insulin dependent diabetes mellitus and six non-diabetic patients. There was no history of hypertension or coronary artery stenosis...

2017

The collagen type VI-related disorders are nowadays considered to be a continuum of overlapping phenotypes with Bethlem myopathy at the mild end and Ullrich congenital muscular dystrophy (UCMD) at the severe end. In between these phenotypes there are collagen type VI-related limb-girdle muscular dystrophy and myosclerosis myopathy. Most cases of Bethlem myopathy have autosomal dominant inherita...

Journal: :iranian journal of child neurology 0
goknur haliloglu professor of pediatric neurology, hacettepe children’s hospital,ankara, turkey haluk topaloglu md,professor of pediatric neurology,department of child neurology,ankara, turkey

objective ullrich congenital muscular dystrophy is a rather severe type of congenital muscular dystrophy with early onset features related to motor development. in general it is inherited in autosomal recessive principles, however in the western world mostly seen with de novo dominant mutations in the collagen vi genes. milder form of the condition is the bethlem myopathy. there may be overlap ...

Journal: :Journal of clinical pathology 1997
M Iwahashi A Ooshima R Nakano

AIM To obtain insight into the effects of oestrogen on extracellular matrix (ECM) in the postmenopausal endometrium. METHODS The distribution of the components of the ECM, including collagen types I, III, IV, and VI, and laminin, was investigated in the human postmenopausal endometrium by an indirect immunofluorescence method with specific monoclonal antibodies and a polyclonal antibody. Coll...

1998
Kathleen J. Doane Scott J. Howell David E. Birk

RESULTS. At embryonic day 6, these receptors were present in a diffuse pattern on cells within the cornea and juxtacorneal regions, indicating a migratory phenotype. At embryonic day 14, when the stroma is fully differentiated, a3 and NG2 were localized in a punctate pattern on a subset of corneal fibroblasts, whereas /3j was more ubiquitously expressed. Colocalization of NG2 and type VI collag...

Journal: :Current eye research 1992
E Tamm A Baur E Lütjen-Drecoll

The production and spatial organization of connective tissue components in ciliary muscle cell cultures was studied with immunohistochemical and ultrastructural methods. Antibodies against collagen types IV and VI, fibronectin and laminin were used. Laminin stains as pericellular network surrounding individual muscle cells. Type IV collagen shows positive cytoplasmic staining and only small foc...

Journal: :The Biochemical journal 2011
Sofie Symoens Marjolijn Renard Christelle Bonod-Bidaud Delfien Syx Elisabeth Vaganay Fransiska Malfait Sylvie Ricard-Blum Efrat Kessler Lut Van Laer Paul Coucke Florence Ruggiero Anne De Paepe

The predominant form of type V collagen is the [α1(V)]₂α2(V) heterotrimer. Mutations in COL5A1 or COL5A2, encoding respectively the α1(V)- and α2(V)-collagen chain, cause classic EDS (Ehlers-Danlos syndrome), a heritable connective tissue disorder, characterized by fragile hyperextensible skin and joint hypermobility. Approximately half of the classic EDS cases remain unexplained. Type V collag...

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