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hydroxymethylbilane
Known as:
21H-biline-2,7,12,17-tetrapropanoic acid, 3,8,13,18-tetrakis(carboxymethyl)-5,10,15,22,23,24-hexahydro-19-(hydroxymethyl)-
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Uroporphyrinogens
Narrower (1)
preuroporphyrinogen
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Use of a universal hydroxymethylbilane synthase (HMBS)-based PCR as an endogenous internal control and to enable typing of mammalian DNAs
Lanjing Wei
,
P. Kelly
,
+5 authors
Chengming Wang
Applied Microbiology and Biotechnology
2014
Corpus ID: 17136292
There is a need for an endogenous internal control (EIC) for PCRs to monitor the quality and quantity of DNA in test samples. We…
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2009
2009
Role of two nutritional hepatic markers (insulin‐like growth factor 1 and transthyretin) in the clinical assessment and follow‐up of acute intermittent porphyria patients
Constance Delaby
,
Jordi To-figueras
,
J. Deybach
,
R. Casamitjana
,
H. Puy
,
Carmen Herrero
Journal of Internal Medicine
2009
Corpus ID: 39696671
Objective. Acute intermittent porphyria (AIP) is caused by a deficiency of hydroxymethylbilane synthase. Clinical manifestations…
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2003
2003
A new synthesis of porphobilinogen analogues, inhibitors of hydroxymethylbilane synthase.
Raef A Ahmed
,
F. Leeper
Organic and biomolecular chemistry
2003
Corpus ID: 20001928
Two analogues of porphobilinogen, the 6-methyl and 6,11-ethano derivatives, have been made by a new synthetic route and the 6…
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2000
2000
Two deletion mutations in the hydroxymethylbilane synthase gene in two unrelated Japanese patients with acute intermittent porphyria
N. Maeda
,
Y. Horie
,
+5 authors
M. Kondo
Journal of Human Genetics
2000
Corpus ID: 3255653
AbstractAcute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of…
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1997
1997
Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthase.
P. Ong
,
W. Lanyon
,
+4 authors
J. Connor
Molecular and Cellular Probes
1997
Corpus ID: 25430398
Acute intermittent porphyria (AIP) is an inborn error of haem biosynthesis caused by a variety of mutations in the gene coding…
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1995
1995
Uroporphyrinogen-III synthase: molecular cloning, nucleotide sequence, expression of a mouse full-length cDNA, and its localization on mouse chromosome 7.
Weiming Xu
,
Christine A. Kozak
,
Robert J. Desnick
Genomics
1995
Corpus ID: 35563122
Highly Cited
1991
Highly Cited
1991
Studies on the mechanism of hydroxymethylbilane synthase concerning the role of arginine residues in substrate binding.
M. Lander
,
A. Pitt
,
P. Alefounder
,
D. Bardy
,
C. Abell
,
A. Battersby
Biochemical Journal
1991
Corpus ID: 35358528
The role of conserved arginine residues in hydroxymethylbilane synthase was investigated by replacing these residues in the…
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Highly Cited
1987
Highly Cited
1987
Purification and properties of uroporphyrinogen III synthase from human erythrocytes.
S. Tsai
,
D. Bishop
,
R. Desnick
Journal of Biological Chemistry
1987
Corpus ID: 22183333
1986
1986
Assaying erythrocyte haem biosynthetic enzyme activities by high-performance liquid chromatography with the advanced automated sample processor.
C. Lim
,
F. Li
,
J. Rideout
,
D. Wright
,
T. Peters
Journal of Chromatography A
1986
Corpus ID: 24090019
Highly Cited
1985
Highly Cited
1985
Purification and properties of uroporphyrinogen III synthase (co-synthetase) from Euglena gracilis.
Graham J. HARTt
,
A. Battersby
Biochemical Journal
1985
Corpus ID: 8449230
Uroporphyrinogen III synthase (co-synthetase) purified from Euglena gracilis is a monomer of Mr 38 500 by gel-filtration studies…
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