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Scholar Results 1 - 10 of about 101 related to Chen: Distribution of the collagen IV isoforms in human Bruch’s membrane. (0.15 sec) 

Distribution of the collagen IV isoforms in human Bruch's membrane

- nih.gov
L Chen, N Miyamura, Y Ninomiya, JT Handa - British Journal of Ophthalmology, 2003 - bjo.bmj.com
Results: In Bruch's membrane, the α1(IV) and α2(IV) chains were identified in
retinal pigment epithelial (10/18 = 55%) and choriocapillaris basement membranes
(18/18 = 100%); the α3(IV), α4(IV), and α5(IV) chains were also found in ...
Cited by 10 - Related articles - BL Direct - All 6 versions

Distribution of the collagen IV isoforms in human Bruch's membrane


LCNMY Ninomiya, JT Handa - 英国眼科学杂志, 2003 - journal.shouxi.net
Results: In Bruch's membrane, the 1(IV) and 2(IV) chains were identified in
retinal pigment epithelial (10/18 = 55%) and choriocapillaris basement membranes
(18/18 = 100%); the 3(IV), 4(IV), and 5(IV) chains were also found in the ...
Related articles - Cached

Distribution of the collagen IV isoforms in human Bruch $# x02019; s membrane


L Chen, N Miyamura, Y Ninomiya, JT Handa - The British Journal of Ophthalmology, 2003 - ukpmc.ac.uk
Results: In Bruch's membrane, the α1(IV) and α2(IV) chains were identified in
retinal pigment epithelial (10/18 = 55%) and choriocapillaris basement membranes
(18/18 = 100%); the α3(IV), α4(IV), and α5(IV) chains were also found in ...
Related articles

Symmetrical reduced retinal thickness in a patient with Alport syndrome


T Usui, M Ichibe, S Hasegawa, A Miki, E Baba … - Retina, 2004 - journals.lww.com
Limited macular translocation is an effective surgical procedure for subfoveal
choroidal neovascularization (CNV) of less than one disk diameter without
requir- ing large retinotomies.1– 4 However, various postoper- ative ...
Cited by 5 - Related articles - All 2 versions

The use of ocular abnormalities to diagnose X-linked Alport syndrome in children


KW Zhang, D Colville, R Tan, C Jones, SI … - Pediatric Nephrology, 2008 - Springer
Abstract The diagnosis of X-linked Alport syndrome is often difficult, but the
demonstration of lenticonus and retinopathy may facilitate the diagnosis in
adult patients. The aim of this study was to determine the diagnostic ...
Cited by 5 - Related articles - All 3 versions

Intermolecular reducible cross-links in rat glomerular basement membrane


VY Wu, MP Cohen - Kidney and Blood Pressure Research, 1983 - content.karger.com
Glomerular basement membrane (GBM) was purified from adult rats and treated with
tritiated borohyride for analysis of the reducible cross-links. After acid
hydrolysis, samples were subjected, with and without prior gel filtration ...
Cited by 2 - Related articles - All 5 versions

[CITATION] New functions for non-collagenous domains of basement membrane collagens


N Ortega, Z Werb - J. Cell. Biol, 2002
Cited by 2 - Related articles

Partial characterization of the heteropolysaccharide associated with the 7S domain of type …


JRA Leushner - Biochemistry and Cell Biology, 1987 - article.pubs.nrc-cnrc.gc.ca
Nous avons noté une certaine microhétérogénéité quant à l'addition de
résidus de fucose et d'acide sialique. L'analyse des composants polypeptidiques
de la fraction 7S après traitement avec une endoglycosidase suggère que ...
Cited by 3 - Related articles - Cached - All 3 versions

Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport …

- oxfordjournals.org
EA Shaw, D Colville, YY Wang, KW Zhang, H … - Nephrology Dialysis Transplantation, 2007 - ERA-EDTA
Results. Ten males and nine females with X-linked Alport syndrome and seven with
autosomal recessive disease were studied. Of the 26 patients, 16 had central
retinopathy (62%), and 19 patients had peripheral retinopathy (74%). The ...
Cited by 10 - Related articles - BL Direct - All 4 versions

[CITATION] Disorders of the basement membrane: hereditary nephritis


FA Flinter - Inherited Disorders of the Kidney: Investigation and …, 1998 - Oxford University Press, USA
Cited by 4 - Related articles


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