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GM01391 Fibroblast

Description:

HURLER SYNDROME

Affected:

Yes

Sex:

Female

Age:

9 MO (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Lysosomal Storage Diseases
Class Disorders of Carbohydrate Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race White
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; alpha-L-iduronidase deficiency; unaffected mother (GM01392) and father (GM01393) also in repository.

Characterizations

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Passage Frozen 6
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 
L-iduronidase According to the submitter, biochemical test results for this subject showed decreased enzyme activity. EC Number: 3.2.1.76
 

Phenotypic Data

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Remarks Clinically affected; alpha-L-iduronidase deficiency; unaffected mother (GM01392) and father (GM01393) also in repository.

Publications

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Prince WS, McCormick LM, Wendt DJ, Fitzpatrick PA, Schwartz KL, Aguilera AI, Koppaka V, Christianson TM, Vellard MC, Pavloff N, Lemontt JF, Qin M, Starr CM, Bu G, Zankel TC, Lipoprotein receptor binding, cellular uptake and lysosomal delivery of fusions between the receptor-associated protein (RAP) and alpha-L-iduronidase or acid alpha-glucosidase. J Biol ChemEpub ahead of print: 2004
PubMed ID: 15170390
 
Hansell EJ, Frisch SM, Tremble P, Murnane JP, Werb Z, Simian virus 40 transformation alters the actin cytoskeleton, expression of matrix metalloproteinases and inhibitors of metalloproteinases, and invasive behavior of normal and ataxia- telangiectasia human skin fibroblasts. Biochem Cell Biol73:373-89 1995
PubMed ID: 8703410
 
Di Natale P, Murino P, Pontarelli G, Salvatore D, Andria G, Sanfilippo B syndrome (MPS III B): altered residual alpha-N- acetylglucosaminidase activity in an unusual sibship. Clin Chim Acta122:135-43 1982
PubMed ID: 6809360
 
Tietze F, Butler JD, Elevated cystine levels in cultured skin fibroblasts from patients with I-cell disease. Pediatr Res13:1350-5 1979
PubMed ID: 523195

External Links

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dbSNP dbSNP ID: 10399
GEO GEO Accession No: GSM1266965
GEO Accession No: GSM1267046
GEO Accession No: GSM651172
GEO Accession No: GSM651173
NCBI GTR 607014 HURLER SYNDROME
OMIM 607014 HURLER SYNDROME
Omim Description HURLER SYNDROME

Images

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View pedigree 

Culture Protocols

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Passage Frozen 6
Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Heat Inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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