Literature DB >> 813230

The mucopolysaccharidoses (a review).

A Dorfman, R Matalon.   

Abstract

The mucopolysaccharidoses are a group of genetic diseases characterized by storage of incompletely degraded glycosaminoglycans. Such storage causes marked distortion of many tissues with consequent severe somatic changes and mental retardation. Storage of glycosaminoglycans results from markedly diminished activity of specific hydrolases requisite for the normal degradation of glycosaminoglycans. The specific enzymic defects have been identified in nine different diseases. In some cases evidence has been obtained indicating the existence of additional allelic diseases based on the same enzyme. The knowledge obtained from these studies has made prenatal diagnosis possible and has led to the possibility that therapy may be undertaken utilizing enzyme replacement.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 813230      PMCID: PMC335965          DOI: 10.1073/pnas.73.2.630

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  68 in total

1.  [A NEW DYSOSTOSIS WITH URINARY ELIMINATION OF CHONDROITIN SULFATE B].

Authors:  P MAROTEAUX; B LEVEQUE; J MARIE; M LAMY
Journal:  Presse Med       Date:  1963-09-25       Impact factor: 1.228

2.  Excretion of sulfated mucopolysaccharides in gargoylism (Hurler's syndrome).

Authors:  K MEYER; M M GRUMBACH; A LINKER; P HOFFMAN
Journal:  Proc Soc Exp Biol Med       Date:  1958-02

3.  A newly recognized forme fruste of Hurler's disease (gargoylism).

Authors:  H G SCHEIE; G W HAMBRICK; L A BARNESS
Journal:  Am J Ophthalmol       Date:  1962-05       Impact factor: 5.258

4.  Isolation and identification of keratosulphate in urine of patients affected by Morquio-Ullrich disease.

Authors:  V PEDRINI; L LENNZI; V ZAMBOTTI
Journal:  Proc Soc Exp Biol Med       Date:  1962 Aug-Sep

5.  Sickle cell anemia a molecular disease.

Authors:  L PAULING; H A ITANO
Journal:  Science       Date:  1949-11-25       Impact factor: 47.728

6.  A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes.

Authors:  S Hickman; E F Neufeld
Journal:  Biochem Biophys Res Commun       Date:  1972-11-15       Impact factor: 3.575

7.  Structure of the "keratosulfate-like" material in liver from a patient with G M1 -gangliosidosis ( -D-galactosidase deficiency).

Authors:  G C Tsay; G Dawson
Journal:  Biochem Biophys Res Commun       Date:  1973-06-08       Impact factor: 3.575

8.  Structure of pig skin dermatan sulfate. 2. Demonstration of sulfated iduronic acid residues.

Authors:  A Malmström; L A Fransson
Journal:  Eur J Biochem       Date:  1971-02-01

9.  The Hunter syndrome in a 46 XX girl.

Authors:  A Milunsky; E F Neufeld
Journal:  N Engl J Med       Date:  1973-01-11       Impact factor: 91.245

10.  Clinical and probable genetic heterogeneity within mucopolysaccharidosis. II. Report of a family with a mild form.

Authors:  J R Lichtenstein; G L Bilbrey; V A McKusick
Journal:  Johns Hopkins Med J       Date:  1972-12
View more
  30 in total

Review 1.  Oxidative depolymerization of polysaccharides by reactive oxygen/nitrogen species.

Authors:  Jinyou Duan; Dennis L Kasper
Journal:  Glycobiology       Date:  2010-10-28       Impact factor: 4.313

2.  Taiwan National Newborn Screening Program by Tandem Mass Spectrometry for Mucopolysaccharidoses Types I, II, and VI.

Authors:  Min-Ju Chan; Hsuan-Chieh Liao; Michael H Gelb; Chih-Kuang Chuang; Mei-Ying Liu; Hsiao-Jan Chen; Shu-Min Kao; Hsiang-Yu Lin; You-Hsin Huang; Arun Babu Kumar; Naveen Kumar Chennamaneni; Nagendar Pendem; Shuan-Pei Lin; Chuan-Chi Chiang
Journal:  J Pediatr       Date:  2018-11-06       Impact factor: 4.406

3.  Spondyloepiphyseal dysplasias and bilateral legg-calvé-perthes disease: diagnostic considerations for mucopolysaccharidoses.

Authors:  Nancy J Mendelsohn; Timothy Wood; Rebecca A Olson; Renee Temme; Susan Hale; Haoyue Zhang; Lisa Read; Klane K White
Journal:  JIMD Rep       Date:  2013-05-09

4.  Characterization of proteins structurally related to human N-acetyl-beta-D-glucosaminidase.

Authors:  M Carroll
Journal:  Biochem J       Date:  1978-07-01       Impact factor: 3.857

5.  Biochemical and genetic factors in the heat inactivation of murine beta-glucuronidase.

Authors:  K Herrup; R J Mullen
Journal:  Biochem Genet       Date:  1977-08       Impact factor: 1.890

6.  A new variety of spondyloepiphyseal dysplasia characterized by punctate corneal dystrophy and abnormal dermal collagen fibrils.

Authors:  P H Byers; K A Holbrook; J G Hall; P Bornstein; J W Chandler
Journal:  Hum Genet       Date:  1978-01-19       Impact factor: 4.132

7.  Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.

Authors:  R M Shull; R J Munger; E Spellacy; C W Hall; G Constantopoulos; E F Neufeld
Journal:  Am J Pathol       Date:  1982-11       Impact factor: 4.307

8.  Suramin-induced storage disease. Mucopolysaccharidosis.

Authors:  G Constantopoulos; S Rees; B G Cragg; J A Barranger; R O Brady
Journal:  Am J Pathol       Date:  1983-11       Impact factor: 4.307

9.  [Influence of glycosaminoglycan synthesis of cultured cornea stroma cells by variation of culture condition].

Authors:  H Bleckmann; H Kresse
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1979-06-15

10.  Morphologic and biochemical studies of canine mucopolysaccharidosis I.

Authors:  R M Shull; R G Helman; E Spellacy; G Constantopoulos; R J Munger; E F Neufeld
Journal:  Am J Pathol       Date:  1984-03       Impact factor: 4.307

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.