Mutations in ABCB6 cause dyschromatosis universalis hereditaria (Q28594264)

GOA release 2020-03-11

Jun Wang

20

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Mingyan Fang

object named as

Mingyan Fang

11

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Yang Huanming

18

object named as

Huanming Yang

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31 January 2017

Caie Zhang

1

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31 January 2017

Duanzhuo Li

2

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31 January 2017

Jianguo Zhang

3

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31 January 2017

Xingping Chen

4

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31 January 2017

Mi Huang

5

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31 January 2017

Stephen Archacki

6

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31 January 2017

Yuke Tian

7

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31 January 2017

Weiping Ren

8

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31 January 2017

Aihua Mei

9

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31 January 2017

Qingyan Zhang

10

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31 January 2017

Zheng Su

12

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31 January 2017

Ye Yin

13

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31 January 2017

Dongxian Liu

14

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31 January 2017

Yingling Chen

15

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31 January 2017

Xiukun Cui

16

1 reference

31 January 2017

Chang Li

17

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31 January 2017

Qing Wang

19

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31 January 2017

Mugen Liu

21

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31 January 2017

Yunhua Deng

Journal of Investigative Dermatology

22

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31 January 2017

language of work or name

English

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publication date

1 September 2013

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31 January 2017

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31 January 2017

133

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31 January 2017

2221–2228

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31 January 2017

9

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31 January 2017

Malignant effusions and immunogenic tumour-derived exosomes

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria: report of a case and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria: an electron microscopic examination

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Shifting the paradigm: the putative mitochondrial protein ABCB6 resides in the lysosomes of cells and in the plasma membrane of erythrocytes

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Identification of a mammalian mitochondrial porphyrin transporter

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

MTABC3, a novel mitochondrial ATP-binding cassette protein involved in iron homeostasis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Rab27a and Rab27b control different steps of the exosome secretion pathway

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Exosomes--vesicular carriers for intercellular communication

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Human pigmentation genes: identification, structure and consequences of polymorphic variation

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

A lumenal domain-dependent pathway for sorting to intralumenal vesicles of multivesicular endosomes involved in organelle morphogenesis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

ATP-dependent mitochondrial porphyrin importer ABCB6 protects against phenylhydrazine toxicity.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

https://api.crossref.org/works/10.1038%2FJID.2013.145

1 reference

7 January 2021

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Dyschromatosis universalis hereditaria: two cases in a Chinese family

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

ABCB6 mutations cause ocular coloboma

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

Involvement of dynein and spectrin with early melanosome transport and melanosomal protein trafficking

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021

A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2013.145

7 January 2021