نتایج جستجو برای: maroteaux

تعداد نتایج: 191  

Journal: :Human molecular genetics 2013
Krista A Geister Michelle L Brinkmeier Minnie Hsieh Susan M Faust I Jill Karolyi Joseph E Perosky Kenneth M Kozloff Marco Conti Sally A Camper

We discovered a new spontaneous mutant allele of Npr2 named peewee (pwe) that exhibits severe disproportionate dwarfism and female infertility. The pwe phenotype is caused by a four base-pair deletion in exon 3 that generates a premature stop codon at codon 313 (L313X). The Npr2(pwe/pwe) mouse is a model for the human skeletal dysplasia acromesomelic dysplasia, Maroteaux type (AMDM). We conduct...

Journal: :Molecular genetics and metabolism 2007
Elena Garrido Amparo Chabás Maria Josep Coll Mariana Blanco Carmen Domínguez Daniel Grinberg Lluïsa Vilageliu Bru Cormand

Maroteaux-Lamy syndrome, or mucopolysaccharidosis VI (MPS VI), is an autosomal recessive lysosomal storage disorder caused by a deficiency of N-acetylgalactosamine-4-sulfatase or arylsulfatase B (ARSB). We aimed to analyze the spectrum of mutations responsible for the disorder in Spanish and Argentinian patients, not previously studied. We identified all the ARSB mutant alleles, nine of them no...

Journal: :Blood 1998
G L Vanham G Penne C Vereecken J Vingerhoets L Kestens

involves the fibroblast growth-factor receptor 3 gene. Blood 10:4062, 1997 9. Tavormina PL, Shiang R, Thompson LM, Zhu YZ, Wilkin DJ, Lachman RS, Wilcox WR, Rimoin DL, Cohn DH, Wasmuth JJ: Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nat Genet 9:321, 1995 10. Caligaris-Cappio F, Bergui L, Gregoretti MG, Gaidano G, Gaboli M, Schena...

Journal: :Journal of medical genetics 1971
R M Bannerman G B Ingall J F Mohn

The syndrome of short stature inherited as an X-linked recessive trait was first reported by Jacobsen (1939) who described one family under the title 'hereditary osteochondrodystrophia deformans'. Three more pedigrees were studied by Maroteaux, Lamy, and Bernard (1957), who proposed the name dysplasia spondyloepiphysaire tardive, or spondyloepiphyseal dysplasia tarda (SDT). These authors also d...

Journal: :The Biochemical journal 1990
J A Taylor G J Gibson D A Brooks J J Hopwood

The biosynthesis and maturation of N-acetylgalactosamine-4-sulphatase (4-sulphatase) was studied in normal fibroblasts and in fibroblasts from patients with either mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) or multiple sulphatase deficiency (MSD). Fibroblasts were incubated in culture medium containing [3H]leucine or [35S]methionine, and radiolabelled 4-sulphatase was isola...

Journal: :Molecular genetics and metabolism 2015
Yew Sing Choy Kaustuv Bhattacharya Shanti Balasubramaniam Michael Fietz Antony Fu Anita Inwood Dong-Kyu Jin Ok-Hwa Kim Motomichi Kosuga Young Hee Kwun Hsiang-Yu Lin Shuan-Pei Lin Nancy J Mendelsohn Torayuki Okuyama Hasri Samion Adeline Tan Akemi Tanaka Verasak Thamkunanon Meow-Keong Thong Teck-Hock Toh Albert D Yang Jim McGill

Mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy syndrome) is caused by deficient activity of the enzyme, N-acetylgalactosamine-4-sulfatase, resulting in impaired degradation of the glycosaminoglycan dermatan sulfate. Patients experience a range of manifestations including joint contractures, short stature, dysostosis multiplex, coarse facial features, decreased pulmonary function, cardiac abno...

Journal: :Journal of medical genetics 1971
M H Shokeir C S Houston C F Awen

Asphyxiating thoracic dystrophy of the newborn is a rare skeletal abnormality. Though the disease is generalized in distribution, the cartilaginous thoracic cage bears the brunt, with the results that the chest is narrow and immobile. The outcome is usually fatal early in the neonatal period. Less frequently the patients survive with severely impaired respiratory function only to succumb to rep...

2006
C. F. AWEN

Asphyxiating thoracic dystrophy of the newborn is a rare skeletal abnormality. Though the disease is generalized in distribution, the cartilaginous thoracic cage bears the brunt, with the results that the chest is narrow and immobile. The outcome is usually fatal early in the neonatal period. Less frequently the patients survive with severely impaired respiratory function only to succumb to rep...

2009
Regina P El Dib Gregory M Pastores

INTRODUCTION Mucopolysaccharidosis type VI (MPS VI, Maroteaux-Lamy syndrome) is an autosomal recessive lysosomal storage disorder, characterized primarily by skeletal dysplasia and joint contracture. It is caused by a deficiency of N-acetylgalactosamine-4-sulfatase (arylsulfatase B), for which a recombinant formulation (galsulfase) is available as replacement therapy. OBJECTIVE To evaluate th...

Journal: :The Journal of Experimental Medicine 1970
B. Shannon Danes J. E. Scott Alexander G. Bearn

Staining with Alcian blue in various concentrations of magnesium chloride (alcianophilia) has been found to be a useful supplement to metachromatic staining to detect increased cellular concentrations of glycosaminoglycans (mucopolysaccharides). In many instances alcianophilia at 0.3 M MgCl(2) is more specific than metachromasia and does not give "false positives" sometimes found in normal indi...

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