(Q53394564)

13 May 2018

title

Equilibrative nucleoside transporter 3 deficiency perturbs lysosome function and macrophage homeostasis. (English)

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13 May 2018

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Chia-Lin Hsu

1

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author name string

Weiyu Lin

2

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13 May 2018

Dhaya Seshasayee

3

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13 May 2018

Yung-Hsiang Chen

4

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13 May 2018

Xiao Ding

5

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13 May 2018

Zhonghua Lin

6

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13 May 2018

Eric Suto

7

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13 May 2018

Zhiyu Huang

8

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13 May 2018

Wyne P Lee

9

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13 May 2018

Hyunjoo Park

10

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13 May 2018

Min Xu

11

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13 May 2018

Mei Sun

12

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13 May 2018

Linda Rangell

13

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13 May 2018

Jeff L Lutman

14

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13 May 2018

Sheila Ulufatu

15

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13 May 2018

Eric Stefanich

16

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13 May 2018

Cecile Chalouni

17

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13 May 2018

Meredith Sagolla

18

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13 May 2018

Lauri Diehl

19

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13 May 2018

Paul Fielder

20

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13 May 2018

Brian Dean

21

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13 May 2018

Mercedesz Balazs

22

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13 May 2018

Flavius Martin

23

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13 May 2018

language of work or name

English

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publication date

15 December 2011

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13 May 2018

number of pages

4

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based on heuristic

inferred from page(s)

published in

Science

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13 May 2018

volume

335

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13 May 2018

issue

6064

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13 May 2018

page(s)

89-92

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13 May 2018

The equilibrative nucleoside transporter family, SLC29

cites work

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Nucleoside transporter proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

The macrophage marches on its phagosome: dynamic assays of phagosome function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Common and uncommon pathogenic cascades in lysosomal storage diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Lysosomal transport disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

The cell biology of lysosomal storage disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

A mouse knockout library for secreted and transmembrane proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Lysosomal fusion and SNARE function are impaired by cholesterol accumulation in lysosomal storage disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Human equilibrative nucleoside transporter-3 (hENT3) spectrum disorder mutations impair nucleoside transport, protein localization, and stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Effect of weak bases on the intralysosomal pH in mouse peritoneal macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Macrophage colony stimulating factor: not just for macrophages anymore! A gateway into complex biologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Macrophages specifically regulate the concentration of their own growth factor in the circulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

The Cbl protooncoprotein stimulates CSF-1 receptor multiubiquitination and endocytosis, and attenuates macrophage proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

A case of H syndrome showing immunophenotye similarities to Rosai-Dorfman disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

Expanding the clinical spectrum of SLC29A3 gene defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1213682

21 January 2018

Identifiers

DOI

10.1126/SCIENCE.1213682

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13 May 2018

PubMed ID

22174130

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13 May 2018