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IDUA gene
Known as:
IDURONIDASE, ALPHA-L
, IDUA
, ALPHA-L-IDURONIDASE
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This gene plays a role in glycosaminoglycan metabolism.
National Institutes of Health
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Related topics
Related topics
3 relations
Carbohydrate Metabolism
Hydrolysis
L-Iduronidase
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
Enzyme replacement therapy started at birth improves outcome in difficult-to-treat organs in mucopolysaccharidosis I mice.
G. Baldo
,
F. Q. Mayer
,
+7 authors
R. Giugliani
Molecular Genetics and Metabolism
2013
Corpus ID: 39161711
Highly Cited
2012
Highly Cited
2012
The designer aminoglycoside NB84 significantly reduces glycosaminoglycan accumulation associated with MPS I-H in the Idua-W392X mouse.
Dan Wang
,
V. Belakhov
,
+5 authors
K. Keeling
Molecular Genetics and Metabolism
2012
Corpus ID: 9453963
Highly Cited
2011
Highly Cited
2011
Reversal of lysosomal storage in brain of adult MPS-I mice with intravenous Trojan horse-iduronidase fusion protein.
R. Boado
,
E. Hui
,
Jeff Zhiqiang Lu
,
Qing-hui Zhou
,
W. Pardridge
Molecular Pharmaceutics
2011
Corpus ID: 10576391
A mouse model of mucopolysaccharidosis (MPS) type I, which is null for the lysosomal enzyme, α-L-iduronidase (IDUA), is treated…
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Highly Cited
2010
Highly Cited
2010
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation.
Dan Wang
,
Charu Shukla
,
+4 authors
K. Keeling
Molecular Genetics and Metabolism
2010
Corpus ID: 46080953
Highly Cited
2008
Highly Cited
2008
Genetic engineering of a lysosomal enzyme fusion protein for targeted delivery across the human blood‐brain barrier
R. Boado
,
Yun Zhang
,
Yu-feng Zhang
,
Chun‐fang Xia
,
Yuntao Wang
,
W. Pardridge
Biotechnology and Bioengineering
2008
Corpus ID: 21131059
Mucopolysaccharidosis Type I, Hurler's Syndrome, is a lysosomal storage disorder that affects the brain. The missing enzyme, α‐L…
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Highly Cited
2005
Highly Cited
2005
Gene therapy for a mucopolysaccharidosis type I murine model with lentiviral-IDUA vector.
C. Di Domenico
,
G. Villani
,
+4 authors
P. di Natale
Human Gene Therapy
2005
Corpus ID: 25167904
Mucopolysaccharidosis type I is a lysosomal disease due to mutations in the IDUA gene, resulting in deficiency of alpha-L…
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1999
1999
Identification and characterization of the molecular lesion causing mucopolysaccharidosis type I in cats.
X. He
,
C. M. Li
,
+4 authors
E. Schuchman
Molecular Genetics and Metabolism
1999
Corpus ID: 35942225
Mucopolysaccharidosis Type I (MPS I) is the lysosomal storage disease caused by the deficient activity of alpha-L-iduronidase…
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1998
1998
Identifying the Source of Mean and Volatility Spillovers in Irish Equities: A Multivariate GARCH Analysis*
Liam A. Gallagher
,
C. Twomey
1998
Corpus ID: 17758129
This paper, using a multivariate VAR-GARCH analysis, examines the role of the UK stock market in the price behaviour of the ten…
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1996
1996
Mapping Disease Risk Estimates Based on Small Numbers: An Assessment of Empirical Bayes Techniques*
D. Pringle
1996
Corpus ID: 55104677
Choropleth maps are frequently used to analyse spatial variations in the risk of a disease. In such maps the relative risk is…
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Highly Cited
1994
Highly Cited
1994
The gene for achondroplasia maps to the telomeric region of chromosome 4p
M. Velinov
,
S. Slaugenhaupt
,
I. Stoilov
,
C. Scott
,
J. Gusella
,
P. Tsipouras
Nature Genetics
1994
Corpus ID: 33378465
Achondroplasia is the most common type of genetic dwarfism. It is characterized by disproportionate short stature and other…
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