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Biotinidase
Known as:
Biocytin Hydrolase
, Biotinidase [Chemical/Ingredient]
, Hydrolase, Biocytin
An enzyme which catalyzes the release of BIOTIN from biocytin. In human, defects in the enzyme are the cause of the organic acidemia MULTIPLE…
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National Institutes of Health
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Related topics
Related topics
20 relations
Broader (1)
Amidohydrolases
BTD gene
Biotinidase Deficiency
Biotinidase deficiency:Imp:Pt:Bld.dot:Nom
Biotinidase:CCnc:Pt:Bld.dot:Qn
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Correlations of Plasma Biotinidase Levels with Hepatic Synthetic Functions in Children with Chronic Liver Diseases
T. Saleem
,
H. Eltalawy
,
+4 authors
Hussein M. Eldeeb
2017
Corpus ID: 79582102
Aims: Certain liver diseases can cause decreased synthesis of liver proteins or enzymes, including biotinidase, thereby reducing…
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2015
2015
Análise do promotor, 5’UTR e éxon 1 do gene BTD em pacientes brasileiros com deficiência de biotinidase.
S. E. Lima
2015
Corpus ID: 90422473
→ Na deficiência de biotinidase (DB), doença de herança autossômica recessiva, estão prejudicadas a absorção e a reutilização da…
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2014
2014
Deficiencia de la actividad de biotinidasa en la población de recién nacidos del Hospital Materno Infantil Ramón Sardá
S. Parsehian
,
María I. Otegui
,
+4 authors
L. Bay
2014
Corpus ID: 73019221
Biotinidase’s Deficiency is an autosomal recessive disorder of metabolism caused by the absence or deficiency of the enzyme. The…
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Review
2013
Review
2013
An update on diagnostic value of biotinidase: From liver damage tocancer: Minireview.
M. Faith
,
P. Abraham
2013
Corpus ID: 13813615
The discovery of biotinidase (BTD) deficiency, an inherited biotin-responsive disorder has increased the interest in biotinidase…
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2010
2010
Triagem neonatal para deficiencia de biotinidase no estado de Minas Gerais
Marilis Tissot Lara
2010
Corpus ID: 203817785
Introducao: a deficiencia de biotinidase e uma doenca metabolica hereditaria, com heranca autossomica recessiva, causada por…
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2006
2006
Leigh syndrome: an uncommon manifestation caused by biotinidase-deficiency
D. Pohl
,
K. Brockmann
,
H. Rustenbeck
,
F. Hanefeld
2006
Corpus ID: 80557366
2000
2000
Clinical chemistry devices; classification of the biotinidase test system. Food and Drug Administration, HHS. Final rule.
Federal register
2000
Corpus ID: 25015000
The Food and Drug Administration (FDA) is classifying the biotinidase test system into class II (special controls). The special…
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1993
1993
Déficit en biotinidase. Une encéphalopathie progressive curable par la biotine.
B. Héron
,
A. Gautier
,
O. Dulac
,
G. Ponsot
1993
Corpus ID: 69124289
BACKGROUND: Multiple carboxylase deficiency is a rare cause of progressive encephalopathy. There are 2 forms: the neonatal-onset…
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Review
1989
Review
1989
Vitamins and inherited human errors of metabolism.
C. Bachmann
International journal for vitamin and nutrition…
1989
Corpus ID: 9886681
Vitamin therapy for inborn errors of metabolism has been used in thiamin-responsive maple syrup urine disease, homocystinuria…
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1969
1969
Biocytin-Sepharoseカラムを用いるAvidinの1工程による精製, Cuatrecasas, P., Wilchek, M., Biochem. Biophys. Res. Comm. 38,235,1968
高田
1969
Corpus ID: 83453857