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A defect in the nuclear translocation of CIITA causes a form of type II bare lymphocyte syndrome
scientific article published on 01 February 1999
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Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
title
A defect in the nuclear translocation of CIITA causes a form of type II bare lymphocyte syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
main subject
Bare lymphocyte syndrome
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author name string
D E Cressman
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
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11 November 2019
K C Chin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
D J Taxman
series ordinal
3
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stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
J P Ting
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
publication date
1 February 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
published in
Immunity
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
volume
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
page(s)
163-171
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
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11 November 2019
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Multiple and persistent viral infections in a patient with bare lymphocyte syndrome
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Karyopherin beta2 mediates nuclear import of a mRNA binding protein
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Two novel mutations in the MHC class II transactivator CIITA in a second patient from MHC class II deficiency complementation group A.
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The MHC class II transactivator (CIITA) requires conserved leucine charged domains for interactions with the conserved W box promoter element.
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Tetrahymena histone acetyltransferase A: a homolog to yeast Gcn5p linking histone acetylation to gene activation
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Class II transactivator regulates the expression of multiple genes involved in antigen presentation
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Class II transactivator (CIITA) is sufficient for the inducible expression of major histocompatibility complex class II genes.
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Importance of acidic, proline/serine/threonine-rich, and GTP-binding regions in the major histocompatibility complex class II transactivator: generation of transdominant-negative mutants
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Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
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A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes
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Genetic evidence for a new type of major histocompatibility complex class II combined immunodeficiency characterized by a dyscoordinate regulation of HLA-D alpha and beta chains
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RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency
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Molecular characterization of major histocompatibility complex class II gene expression and demonstration of antigen-specific T cell response indicate a new phenotype in class II-deficient patients
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Bare lymphocyte syndrome: altered HLA class II expression in B cell lines derived from two patients
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In vivo footprinting of MHC class II genes: bare promoters in the bare lymphocyte syndrome
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Protein import into the nucleus
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1 reference
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Regulation of MHC gene expression
1 reference
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reference URL
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Human MHC class II gene transcription directed by the carboxyl terminus of CIITA, one of the defective genes in type II MHC combined immune deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1074-7613%2800%2980017-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1074-7613(00)80017-5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
PubMed publication ID
10072069
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10072069
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10072069%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 November 2019
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