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IMPDH1 gene
Known as:
IMPDH1
, IMP (Inosine Monophosphate) Dehydrogenase 1 Gene
, INOSINE-5-PRIME-MONOPHOSPHATE DEHYDROGENASE, TYPE I
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This gene plays a role in the regulation of cell growth.
National Institutes of Health
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Related topics
Related topics
5 relations
Narrower (1)
IMPDH1 wt Allele
IMPDH1, human
LEBER CONGENITAL AMAUROSIS 11
Nucleotide Metabolism
Oxidation-Reduction
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Genetic variations in the HGPRT, ITPA, IMPDH1, IMPDH2, and GMPS genes in Japanese individuals.
Mutsumi Kudo
,
Yuka Saito
,
+7 authors
M. Hiratsuka
Drug Metabolism and Pharmacokinetics
2009
Corpus ID: 30230517
Thiopurines (such as azathioprine and 6-mercaptopurine) are widely used for the treatment of patients suffering from malignancies…
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2009
2009
Expression of IMPDH1 is regulated in response to mycophenolate concentration.
S. Bremer
,
N. T. Vethe
,
H. Rootwelt
,
S. Bergan
International Immunopharmacology
2009
Corpus ID: 42770120
2007
2007
Further evidence of autosomal-dominant Leber congenital amaurosis caused by heterozygous CRX mutation
Panfeng Wang
,
Xiangming Guo
,
Qingjiong Zhang
Graefe's Archive for Clinical and Experimental…
2007
Corpus ID: 35041816
Dear Editor: Leber congenital amaurosis (LCA; OMIM 204000) is the earliest and most severe form of inherited retinal dystrophy…
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2005
2005
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
Y. Wada
,
M. Sandberg
,
T. L. McGee
,
Melissa A. Stillberger
,
E. Berson
,
T. Dryja
Investigative Ophthalmology and Visual Science
2005
Corpus ID: 16343708
PURPOSE To determine the frequency of mutations in IMPDH1 among patients with autosomal dominant retinitis pigmentosa (RP), to…
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Review
2005
Review
2005
Clinical Phenotype in a Swedish Family with a Mutation in the IMPDH1 Gene
Patrik Schatz
,
V. Ponjavic
,
S. Andreasson
,
T. L. McGee
,
T. Dryja
,
M. Abrahamson
Ophthalmic Genetics
2005
Corpus ID: 33839722
Purpose: Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) have recently been discovered to cause a form of…
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2003
2003
Genetic, ophthalmic, morphometric and histopathological analysis of the Retinopathy Globe Enlarged (rge) chicken.
C. Inglehearn
,
D. Morrice
,
+11 authors
D. Burt
Molecular Vision
2003
Corpus ID: 19392776
PURPOSE To identify the locus responsible for rge (retinopathy globe enlarged) in chickens and further characterise the rge…
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2003
2003
On the role of IMPDH1 in retinal degeneration.
A. Kennan
,
A. Aherne
,
+5 authors
A. Kennan
Advances in Experimental Medicine and Biology
2003
Corpus ID: 33287584
To date twelve loci have been associated with the autosomal dominant form of Retinitis Pigmentosa (adRP). The genes at eleven of…
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1994
1994
Assignment of the human type I IMP dehydrogenase gene (IMPDH1) to chromosome 7q31.3-q32).
J. Gu
,
K. Kaiser-Rogers
,
K. Rao
,
B. Mitchell
Genomics
1994
Corpus ID: 36795863
Two phage lambda clones that contain the 5' portion of the human type I inosine 5'-monophosphate dehydrogenase (IMPDH, EC 1.1.1…
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1991
1991
Isolation and sequence of a cDNA encoding mouse IMP dehydrogenase.
A. A. Tiedeman
,
J. Smith
Gene
1991
Corpus ID: 34264259
Highly Cited
1987
Highly Cited
1987
Inosine monophosphate dehydrogenase and myeloid cell maturation.
R. Knight
,
J. Mangum
,
D. Lucas
,
D. Cooney
,
E. Khan
,
D. Wright
Blood
1987
Corpus ID: 14105808
In previous studies of purine ribonucleotide metabolism in the human myeloid leukemia cell line HL-60, we observed that there is…
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