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Scholar Results 1 - 10 of about 101 related to Majid: Tissue inhibitor of metalloproteinase-3 differentially binds to components of Bruch’s.... (0.07 sec) 

Tissue inhibitor of metalloproteinase-3 differentially binds to components of Bruch's …

- nih.gov
MA Majid, VA Smith, FJ Matthews, AC Newby, … - British Journal of Ophthalmology, 2006 - bjo.bmj.com
Background: Sorsby's fundus dystrophy (SFD) is caused by mutations in tissue
inhibitor of metalloproteinase (TIMP)-3 and, with the exception of early onset,
is similar to age-related macular degeneration. The pathological features ...
Cited by 2 - Related articles - BL Direct - All 7 versions

Keratoconus: matrix metalloproteinase-2 activation and TIMP modulation


VA Smith, FJ Matthews, MA Majid, SD Cook - BBA-Molecular Basis of Disease, 2006 - Elsevier
Keratoconus is an ocular condition that causes corneal thinning, cone formation
and scarring. In view of a hypothesis that activated MMP-2 may initiate or
facilitate disease progression, the MMP-2/TIMP systems of stromal cells ...
Cited by 5 - Related articles - All 4 versions

Sorsby's fundus dystrophy mutant tissue inhibitors of metalloproteinase-3 induce apoptosis of …


MA Majid, VA Smith, DL Easty, AH Baker, AC … - FEBS letters, 2002 - Elsevier
C-terminal domain tissue inhibitor of metalloproteinases-3 (TIMP-3) mutations
cause the rare hereditary blindness Sorsby's fundus dystrophy (SFD), which
involves loss of retinal pigment epithelial (RPE) cells. Since wild-type ...
Cited by 15 - Related articles - All 6 versions

Adenovirus mediated gene delivery of tissue inhibitor of metalloproteinases-3 induces death …

- bmj.com
MA Majid, VA Smith, DL Easty, AH Baker, AC … - British Medical Journal, 2002 - bjo.bmj.com
Background: Sorsby's fundus dystrophy (SFD) and age related macular degeneration
(ARMD) are retinal diseases associated with a high level of accumulation of
mutant and wild type TIMP-3, respectively, in Bruch's membrane. The ...
Cited by 21 - Related articles - BL Direct - All 8 versions

TIMP-3, collagen, and elastin immunohistochemistry and histopathology of Sorsby's fundus …

- iovs.org
NH Chong, RA Alexander, T Gin, AC Bird, PJ … - Investigative ophthalmology & visual science, 2000 - ARVO
METHODS. The eyes of an SFD donor with a confirmed TIMP-3 mutation were examined
using histologic techniques demonstrating connective tissue, calcium, and lipid.
Immunohistochemical analyses were performed using antibodies against ...
Cited by 34 - Related articles - BL Direct - All 4 versions

[CITATION] TIMP-3 accumulation in Bruch's membrane and drusen in eyes from normal and age-related …


M Kamei, SS Apte, ME Rayborn, H Lewis, JG … - Degenerative Retinal Diseases, 1997
Cited by 7 - Related articles

Sorsby's fundus dystrophy mutations impair turnover of TIMP-3 by retinal pigment epithelial …

- oxfordjournals.org
KP Langton, N McKie, BM Smith, NJ Brown, … - Human Molecular Genetics, 2005 - Oxford Univ Press
Sorsby's fundus dystrophy (SFD) is an autosomal dominant degenerative disease of
the retina, caused by mutations in exon 5 of the gene for tissue inhibitor of
metalloproteinases-3 (TIMP-3). The mechanism by which these mutations give ...
Cited by 7 - Related articles - BL Direct - All 5 versions

[CITATION] Perspectives for TNF-alpha-targeting therapies http://arthritis-research. com/content/4/S3/ …


HM Lorenz, JR Kalden - ARTHRITIS RESEARCH, 2002 - CURRENT SCIENCE LTD.,
Cited by 1 - Related articles - BL Direct

Matrix bound SFD mutant TIMP-3 is more stable than wild type TIMP-3


MA Majid, VA Smith, AC Newby, AD Dick - British Journal of Ophthalmology, 2007 - bjo.bmj.com
Methods: COS-7 cells were transfected with plasmids containing wild type, Ser
181, Gly-167, Ser-156, and Tyr-168 TIMP-3 cDNA. The cells and their matrices
were subsequently harvested and homogenised. After measuring the bound wild ...
Related articles - BL Direct - All 5 versions

Expression of mutant and wild-type TIMP3 in primary gingival fibroblasts from Sorsby's …


CE Arris, DJ Bevitt, J Mohamed, Z Li, KP … - BBA-Molecular Basis of Disease, 2003 - Elsevier
Gingival fibroblast cell lines were derived from Sorsby's fundus dystrophy (SFD)
patients carrying the S181C TIMP3 and the E139X TIMP3 mutations. These cell
lines were grown in culture to study expression of the wild-type and mutant ...
Cited by 6 - Related articles - All 6 versions


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