(Q33530133)

English

Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease

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scholarly article

1 reference

Europe PubMed Central

27 July 2017

Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease (English)

1 reference

Europe PubMed Central

27 July 2017

12

object named as

Peter Devilee

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Margaret A Knowles

13

object named as

Margaret A Knowles

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David Tannahill

object named as

David Tannahill

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object named as

Neil V Morgan

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Paul Gissen

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Eamonn R Maher

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Richard C Trembath

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Richard C Trembath

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Erol Kismet

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27 July 2017

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Vedat Köseoğlu

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Europe PubMed Central

27 July 2017

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Shanaz Pasha

1 reference

Europe PubMed Central

27 July 2017

author name string

Mark R Morris

2

1 reference

Europe PubMed Central

27 July 2017

Hakan Cangul

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Europe PubMed Central

27 July 2017

Diane Gleeson

4

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Europe PubMed Central

27 July 2017

Anna Straatman-Iwanowska

5

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Europe PubMed Central

27 July 2017

Nicholas Davies

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Europe PubMed Central

27 July 2017

Stephen Keenan

7

1 reference

Europe PubMed Central

27 July 2017

Fatimah Rahman

9

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Europe PubMed Central

27 July 2017

Dean Gentle

10

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Europe PubMed Central

27 July 2017

Maaike P G Vreeswijk

11

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Europe PubMed Central

27 July 2017

Serdar Ceylaner

14

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Europe PubMed Central

27 July 2017

Carlos Dalence

16

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27 July 2017

Hans-Christoph Rossbach

19

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27 July 2017

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5 February 2010

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Europe PubMed Central

27 July 2017

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Europe PubMed Central

27 July 2017

6

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27 July 2017

2

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Europe PubMed Central

27 July 2017

e1000833

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Europe PubMed Central

27 July 2017

copyright license

Creative Commons Attribution 4.0 International

5 February 2010

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April 2022 Public Data File from Crossref

copyright status

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Facilitated mitochondrial import of antiviral and anticancer nucleoside drugs by human equilibrative nucleoside transporter-3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

The H syndrome is caused by mutations in the nucleoside transporter hENT3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Effect of adenosine on the growth of human T-lymphocyte leukemia cell line MOLT-4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Intracellularly transported adenosine induces apoptosis in HuH-7 human hepatoma cells by downregulating c-FLIP expression causing caspase-3/-8 activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Molecular determinants of substrate selectivity of a novel organic cation transporter (PMAT) in the SLC29 family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Succinate dehydrogenase and fumarate hydratase: linking mitochondrial dysfunction and cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Growth inhibitory effect and apoptosis induced by extracellular ATP and adenosine on human gastric carcinoma cells: involvement of intracellular uptake of adenosine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Transcriptional link between blood and bone: the stem cell leukemia gene and its +19 stem cell enhancer are active in bone cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Adenosine induces apoptosis in the human gastric cancer cells via an intrinsic pathway relevant to activation of AMP-activated protein kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

The netrin-1 receptors UNC5H are putative tumor suppressors controlling cell death commitment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Nucleoside analogues in the therapy of Langerhans cell histiocytosis: a survey of members of the histiocyte society and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Histiocytosis--an introduction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Histiocytes and histiocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2816679

21 June 2018

Faisalabad histiocytosis mimics Rosai-Dorfman disease: brothers with lymphadenopathy, intrauterine fractures, short stature, and sensorineural deafness.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000833

21 January 2018

SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000833

21 January 2018

Functional characterization of novel human and mouse equilibrative nucleoside transporters (hENT3 and mENT3) located in intracellular membranes

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000833

21 January 2018

Histiocytosis syndromes in children. Writing Group of the Histiocyte Society

1 reference

https://pubmed.ncbi.nlm.nih.gov/20140240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sinus histiocytosis with massive lymphadenopathy in three brothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/20140240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human equilibrative nucleoside transporter (ENT) family of nucleoside and nucleobase transporter proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/20140240

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1000833

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

1 reference

Europe PubMed Central

27 July 2017

ResearchGate publication ID

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