Equilibrative nucleoside transporter 3 deficiency perturbs lysosome function and macrophage homeostasis. (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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Dhaya Seshasayee

3

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Yung-Hsiang Chen

4

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Xiao Ding

5

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Zhonghua Lin

6

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Eric Suto

7

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Zhiyu Huang

8

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Wyne P Lee

9

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Hyunjoo Park

10

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Min Xu

11

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Mei Sun

12

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Linda Rangell

13

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Jeff L Lutman

14

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Sheila Ulufatu

15

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Eric Stefanich

16

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Cecile Chalouni

17

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Meredith Sagolla

18

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Lauri Diehl

19

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Paul Fielder

20

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Brian Dean

21

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Mercedesz Balazs

22

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Flavius Martin

23

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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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volume

335

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issue

6064

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page(s)

89-92

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13 May 2018

The equilibrative nucleoside transporter family, SLC29

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

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Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function

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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Expanding the clinical spectrum of SLC29A3 gene defects

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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