(Q45119914)

9 December 2017

title

Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A985377

maple syrup urine disease

12 August 2022

main subject

1 reference

2

D P Molden

0 references

author name string

S. D. Skaper

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A985377

12 August 2022

J. E. Seegmiller

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A985377

12 August 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=985377

12 August 2022

publication date

1 August 1976

1 reference

9 December 2017

1 reference

9 December 2017

volume

14

1 reference

9 December 2017

issue

7-8

1 reference

9 December 2017

page(s)

527-539

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00485832

9 December 2017

exact match

0 references

cites work

Studies in maple syrup urine disease

1 reference

12 December 2020

Maple syrup urine disease metabolites studies in cerebellum cultures.

1 reference

12 December 2020

THE DIAGNOSIS OF MAPLE SYRUP URINE DISEASE (BRANCHED- CHAIN KETOACIDURIA) BY THE IN VITRO STUDY OF THE PERIPHERAL LEUKOCYTE

1 reference

12 December 2020

Maple syrup urine disease: branched-chain keto-aciduria

1 reference

12 December 2020

Maple syrup urine disease

1 reference

12 December 2020

The enzyme defect in maple syrup urine disease (branched chain ketoaciduria)

1 reference

12 December 2020

Biochemically Marked Lymphocytoid Lines: Establishment of Lesch-Nyhan Cells

1 reference

12 December 2020

CEREBRAL LIPIDS IN MAPLE SYRUP DISEASE.

1 reference

12 December 2020

Inhibition of brain glutamic acid decarboxylase by phenylalanine, valine, and leucine derivatives: a suggestion concerning the etiology of the neurological defect in phenylketonuria and branched-chain ketonuria.

1 reference

12 December 2020

Inhibition of brain protein synthesis: an approach to the biochemical basis of neurological dysfunction in the amino-acidurias

1 reference

12 December 2020

Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female

1 reference

12 December 2020

Increased concentrations of glycine in hypoxanthine-guanine phosphoribosyltransferase-deficient mouse neuroblastoma cells

1 reference

12 December 2020

Enzyme activity in classical and variant forms of maple syrup urine disease

1 reference

12 December 2020

EFFECT OF AMINO ACIDS ON UPTAKE OF l‐HISTIDINE BY RAT BRAIN SLICES

1 reference

12 December 2020

Influence of alpha-ketoacids on the respiration of brain in vitro.

1 reference

12 December 2020

Defective decarboxylase in branched chain ketoacid oxidase multienzyme complex in classic type of maple syrup urine disease

1 reference

12 December 2020

Brain lipids, proteolipids, and free amino acids in maple syrup urine disease

1 reference

12 December 2020

Intermittent branched chain ketonuria (variant of maple syrup urine disease)

1 reference

12 December 2020

THE METABOLISM OF LEUCINE IN TISSUE CULTURE OF SKIN FIBROBLASTS OF MAPLE-SYRUP-URINE DISEASE

1 reference

12 December 2020

Biochemical studies on branched-chain oxoacid oxidases

1 reference

12 December 2020

Maple syrup disease; isolation and identification of organic acids in the urine

1 reference

12 December 2020

Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency.

1 reference

12 December 2020

A new variant of maple syrup urine disease (branched chain ketoaciduria). Clinical and biochemical evaluation

1 reference

12 December 2020

Serotonin Depletion by Dietary Leucine

1 reference

12 December 2020

A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance.

1 reference

12 December 2020

A study of the transport of 5-hydroxytryptophan and 5-hydroxytryptamine (serotonin) into brain.

1 reference

12 December 2020

Branched chain alpha-keto acid metabolism. I. Isolation, purification, and partial characterization of bovine liver alpha-ketoisocaproic:alpha-keto-beta-methylvaleric acid dehydrogenase

1 reference

12 December 2020

MAPLE SYRUP URINE DISEASE, WITH PARTICULAR REFERENCE TO DIETOTHERAPY

1 reference

12 December 2020

Studies on aromatic amino acid uptake by rat brain in vivo. Uptake of phenylalanine and of tryptophan; inhibition and stereoselectivity in the uptake of tyrosine by brain and muscle.

1 reference

12 December 2020

DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00485832

1 reference

Dimensions Publication ID

9 December 2017

1015398808

0 references

1 reference