The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3 (Q24294330)

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English	The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3	scientific article

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scholarly article

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The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3 (English)

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NGG1 interacting factor 3 like 1

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GOA release 2020-03-11

Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta

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GOA release 2020-03-11

positive regulation of transcription, DNA-templated

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GOA release 2020-03-11

MLX interacting protein-like

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GOA release 2020-03-11

Williams-Beuren syndrome

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based on heuristic

inferred from title

Alexandre Reymond

4

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2

object named as

Cédric Howald

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Stilianos Antonarakis

object named as

Stylianos E Antonarakis

3

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1

object named as

Giuseppe Merla

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language of work or name

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publication date

15 July 2004

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Human Molecular Genetics

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13

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14

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1505-14

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Dietary regulation of gene expression: enzymes involved in carbohydrate and lipid metabolism

1 reference

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21 January 2018

Regulation of the expression of lipogenic enzyme genes by carbohydrate

1 reference

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21 January 2018

Guidelines for human gene nomenclature

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Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein

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Carbohydrate responsive element-binding protein (ChREBP): a key regulator of glucose metabolism and fat storage

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WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network

1 reference

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21 January 2018

WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog

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21 January 2018

A glucose-responsive transcription factor that regulates carbohydrate metabolism in the liver

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The interplay between Mad and Myc in proliferation and differentiation

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Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?

1 reference

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Xylulose 5-phosphate mediates glucose-induced lipogenesis by xylulose 5-phosphate-activated protein phosphatase in rat liver

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The role of SREBP-1c in nutritional regulation of lipogenic enzyme gene expression

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Mlx is the functional heteromeric partner of the carbohydrate response element-binding protein in glucose regulation of lipogenic enzyme genes

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Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

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Natural history of Williams syndrome: physical characteristics

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Williams-Beuren syndrome: genes and mechanisms

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Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder

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A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

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Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

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MondoA, a novel basic helix-loop-helix-leucine zipper transcriptional activator that constitutes a positive branch of a max-like network

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How do 14-3-3 proteins work?-- Gatekeeper phosphorylation and the molecular anvil hypothesis

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Isolation and characterization of a novel human gene, NIF3L1, and its mouse ortholog, Nif3l1, highly conserved from bacteria to mammals

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Identification and characterization of NIF3L1 BP1, a novel cytoplasmic interaction partner of the NIF3L1 protein

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The role of transcriptional corepressor Nif3l1 in early stage of neural differentiation via cooperation with Trip15/CSN2

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14-3-3 proteins: structure, function, and regulation

1 reference

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14-3-3 proteins: regulation of subcellular localization by molecular interference

1 reference

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Leptomycin B inactivates CRM1/exportin 1 by covalent modification at a cysteine residue in the central conserved region

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A novel heterodimerization domain, CRM1, and 14-3-3 control subcellular localization of the MondoA-Mlx heterocomplex.

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NESbase version 1.0: a database of nuclear export signals

1 reference

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Identification of additional transcripts in the Williams-Beuren syndrome critical region

1 reference

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21 January 2018

Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome

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Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis.

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Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice

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Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

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Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion.

1 reference

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Mechanisms by which carbohydrates regulate expression of genes for glycolytic and lipogenic enzymes.

1 reference

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Glucose regulation of gene transcription

1 reference

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Cytoplasmic localization of human cdc25C during interphase requires an intact 14-3-3 binding site

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Regulation of histone deacetylase 4 by binding of 14-3-3 proteins

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Identification of a signal-responsive nuclear export sequence in class II histone deacetylases

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Regulation of histone deacetylase 4 and 5 and transcriptional activity by 14-3-3-dependent cellular localization

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Nuclear localization of Cdc25 is regulated by DNA damage and a 14-3-3 protein

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Specific interaction between 14-3-3 isoforms and the human CDC25B phosphatase

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Transcriptional activation by yeast PDR1p is inhibited by its association with NGG1p/ADA3p.

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Histone-like TAFs within the PCAF histone acetylase complex

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Mechanism for fatty acid "sparing" effect on glucose-induced transcription: regulation of carbohydrate-responsive element-binding protein by AMP-activated protein kinase

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The tripartite motif family identifies cell compartments

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A role for Hsc70 in regulating nucleocytoplasmic transport of a temperature-sensitive p53 (p53Val-135)

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Carbohydrate regulation of hepatic gene expression. Evidence against a role for the upstream stimulatory factor

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based on heuristic

inferred from DOI database lookup

Physiological and molecular mechanisms involved in nutritional regulation of fatty acid synthesis

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7 January 2021

based on heuristic

inferred from DOI database lookup

Williams-Beuren syndrome: a model of recurrent genomic mutation

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1093/HMG/DDH163

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

release_rjtllszz2nc5heclgwcesgb53u

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https://api.fatcat.wiki/v0/release/rjtllszz2nc5heclgwcesgb53u

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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