Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome (Q24652922)

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English	Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome	scientific article

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instance of

scholarly article

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title

Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome (English)

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main subject

clinical chemistry

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author name string

A Ri Cho

series ordinal

1

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Keum Jin Yang

series ordinal

2

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Yoonsun Bae

series ordinal

3

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Young Yil Bahk

series ordinal

4

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Eunmin Kim

series ordinal

5

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Hyungnam Lee

series ordinal

6

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Jeong Ki Kim

series ordinal

7

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Wonsang Park

series ordinal

8

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Hyanshuk Rhim

series ordinal

9

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Soo Young Choi

series ordinal

10

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Tsuneo Imanaka

series ordinal

11

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Sungdae Moon

series ordinal

12

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Jongbok Yoon

series ordinal

13

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Sungjoo Kim Yoon

series ordinal

14

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language of work or name

English

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publication date

30 June 2009

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published in

Experimental and Molecular Medicine

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volume

41

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issue

6

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page(s)

381-6

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cites work

The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome

1 reference

stated in

PubMed Central

reference URL

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7 April 2017

TIP120A associates with cullins and modulates ubiquitin ligase activity

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7 April 2017

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants

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PubMed Central

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7 April 2017

Construction and characterization of a normalized cDNA library

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PubMed Central

reference URL

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7 April 2017

Genotypic heterogeneity and clinical phenotype in triple A syndrome: a review of the NIH experience 2000-2005

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PubMed Central

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7 April 2017

Molecular cloning and characterization of AAAS-V2, a novel splice variant of human AAAS

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PubMed Central

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7 April 2017

Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene

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PubMed Central

reference URL

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7 April 2017

Mutant WD-repeat protein in triple-A syndrome

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PubMed Central

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7 April 2017

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster

1 reference

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PubMed Central

reference URL

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7 April 2017

Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins

1 reference

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PubMed Central

reference URL

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retrieved

28 September 2017

Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima

1 reference

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reference URL

https://pubmed.ncbi.nlm.nih.gov/19322026

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.3858/EMM.2009.41.6.043

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Dimensions Publication ID

1034133506

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PMC publication ID

2705858

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PubMed publication ID

19322026

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ResearchGate publication ID

24234855

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