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BTD gene
Known as:
BIOTINIDASE
, BTD
National Institutes of Health
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Related topics
1 relation
Biotinidase
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Extension of the single amino acid chelate concept (SAAC) to bifunctional biotin analogues for complexation of the M(CO)3(+1) Core (M = Tc and Re): syntheses, characterization, biotinidase stability…
S. James
,
K. Maresca
,
+4 authors
J. Zubieta
Bioconjugate chemistry
2006
Corpus ID: 36006370
Biotin and avidin form one of the most stable complexes known (K(D) = 10(-15) M(-1)) making this pairing attractive for a variety…
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2006
2006
Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota).
K. Hayakawa
,
Lei Guo
,
+8 authors
Toshiaki Tanaka
Journal of chromatography. B, Analytical…
2006
Corpus ID: 33176821
2004
2004
Identification of alternatively spliced human biotinidase mRNAs and putative localization of endogenous biotinidase.
C. Stanley
,
J. Hymes
,
B. Wolf
Molecular Genetics and Metabolism
2004
Corpus ID: 21840703
2002
2002
Biotinidase catalyzes debiotinylation of histones
T. D. Ballard
,
J. Wolff
,
J. B. Griffin
,
J. Stanley
,
Sandy van Calcar
,
J. Zempleni
European Journal of Nutrition
2002
Corpus ID: 23588570
SummaryBackground Posttranslational modifications of histones play important roles in processes such as regulation of gene…
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2002
2002
Seventeen novel mutations that cause profound biotinidase deficiency.
B. Wolf
,
K. Jensen
,
+15 authors
J. Sykut-Cegielska
Molecular Genetics and Metabolism
2002
Corpus ID: 32265721
Highly Cited
1999
Highly Cited
1999
Is pantetheinase the actual identity of mouse and human vanin‐1 proteins?
B. Maras
,
D. Barra
,
S. Dupré
,
G. Pitari
FEBS Letters
1999
Corpus ID: 25738323
1997
1997
Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States.
K. Norrgard
,
R. Pomponio
,
+4 authors
B. Wolf
Biochemical and Molecular Medicine
1997
Corpus ID: 23875955
Biotinidase deficiency is an autosomal recessive disorder that can result in neurologic and cutaneous symptoms if not treated…
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1994
1994
Localization of serum biotinidase (BTD) to human chromosome 3 in band p25.
H. Cole
,
S. Weremowicz
,
C. Morton
,
B. Wolf
Genomics
1994
Corpus ID: 46290820
Biotinidase (EC 3.5.1.12) recycles the vitamin biotin by catalyzing the hydrolysis of biocytin, the product of biotin-dependent…
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Highly Cited
1986
Highly Cited
1986
Purification and characterization of human serum biotinidase.
J. Chauhan
,
K. Dakshinamurti
Journal of Biological Chemistry
1986
Corpus ID: 30664435
Biotinidase has been purified from human serum to a specific activity of 1900 units/mg protein by a five-step procedure. After…
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1985
1985
Neurologic symptoms of biotinidase deficiency
S. Suchy
,
J. McVoy
,
B. Wolf
Neurology
1985
Corpus ID: 5724362
We found that the activity of biotinidase is much lower in human and rat brain or human CSF than in serum or other tissues that…
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