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3-methylglutaric acid
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Meglutol
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
3-Methylglutaric acid as a 13C solid-state NMR standard.
D. Barich
,
E. Gorman
,
M. Zell
,
E. Munson
Solid state nuclear magnetic resonance
2006
Corpus ID: 39921557
The calibration of a solid-state NMR spectrometer requires setting the magic angle, setting the reference and decoupler…
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Review
2004
Review
2004
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)
P. Barth
,
R. Wanders
,
P. Vreken
,
E. Janssen
,
J. Lam
,
F. Baas
Journal of Inherited Metabolic Disease
2004
Corpus ID: 11545874
X-linked cardioskeletal myopathy, neutropenia and abnormal mitochondria (MIM 302060) (synonyms: Barth syndrome, 3…
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Highly Cited
2004
Highly Cited
2004
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract
P. Reynier
,
P. Amati-Bonneau
,
+13 authors
D. Bonneau
Journal of Medical Genetics
2004
Corpus ID: 122110
Hereditary optic atrophy is a generic term that refers to a heterogeneous group of genetic disorders for which several modes of…
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Highly Cited
2002
Highly Cited
2002
3-Methylglutaconic aciduria type I is caused by mutations in AUH.
L. Ijlst
,
F. J. Loupatty
,
J. Ruiter
,
M. Duran
,
W. Lehnert
,
R. Wanders
American journal of human genetics
2002
Corpus ID: 725517
3-Methylglutaconic aciduria type I is an autosomal recessive disorder clinically characterized by various symptoms ranging from…
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Highly Cited
2001
Highly Cited
2001
Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews.
Y. Anikster
,
R. Kleta
,
A. Shaag
,
W. Gahl
,
O. Elpeleg
American journal of human genetics
2001
Corpus ID: 14708299
Type III 3-methylglutaconic aciduria (MGA) (MIM 258501) is a neuro-ophthalmologic syndrome that consists of early-onset bilateral…
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2001
2001
3-Hydroxy-3-methylglutaric aciduria in an Italian patient is caused by a new nonsense mutation in the HMGCL gene.
S. Funghini
,
E. Pasquini
,
+4 authors
E. Zammarchi
Molecular genetics and metabolism
2001
Corpus ID: 10891117
3-Hydroxy-3-methylglutaric aciduria is a rare autosomal recessive inborn error of metabolism caused by deficiency of the…
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Highly Cited
1998
Highly Cited
1998
Selective inhibition of the bacterial peptidoglycan biosynthesis by the new types of liposidomycins.
K. Kimura
,
Y. Ikeda
,
+4 authors
K. Isono
The Journal of antibiotics
1998
Corpus ID: 27374656
We examined the inhibitory activity against bacterial peptidoglycan biosynthesis, mammalian glycoprotein biosynthesis and growth…
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Highly Cited
1982
Highly Cited
1982
Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism.
M. Durán
,
F. Beemer
,
A. S. Tibosch
,
L. Bruinvis
,
D. Ketting
,
S. K. Wadman
The Journal of pediatrics
1982
Corpus ID: 43081831
Two brothers, aged 7 and 5 years, who excreted large amounts of the leucine metabolites 3-methylglutaconic acid, 3-methylglutaric…
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Highly Cited
1976
Highly Cited
1976
The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria.
K. Faull
,
P. Bolton
,
B. Halpern
,
J. Hammond
,
D. Danks
Clinica chimica acta; international journal of…
1976
Corpus ID: 45223874
Abstract The urinary organic acid profile of 3-hydroxy-3-methylglutaric aciduria contains excessive amounts of 3-methylglutaconic…
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1976
1976
3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria.
S. Wysocki
,
S. Wilkinson
,
R. Hähnel
,
C. Wong
,
P. Panegyres
Clinica chimica acta; international journal of…
1976
Corpus ID: 9028473
1. A baby with severe metabolic acidosis was found to excrete abnormal amounts of 3-methylcrotonic acid, 3-methylglutaconic acid…
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