(Q28589444)

English

Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome

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scholarly article

1 reference

Europe PubMed Central

24 June 2017

Mice lacking the nuclear pore complex protein ALADIN show female infertility but fail to develop a phenotype resembling human triple A syndrome (English)

1 reference

Europe PubMed Central

24 June 2017

Achalasia, adrenocortical insufficiency, alacrimia

1 reference

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

4

object named as

Angela M Kaindl

1 reference

Europe PubMed Central

24 June 2017

6

object named as

Paul Verkade

1 reference

Europe PubMed Central

24 June 2017

author name string

Angela Huebner

1

1 reference

Europe PubMed Central

24 June 2017

Philipp Mann

2

1 reference

Europe PubMed Central

24 June 2017

Elvira Rohde

3

1 reference

Europe PubMed Central

24 June 2017

Martin Witt

5

1 reference

Europe PubMed Central

24 June 2017

Sibylle Jakubiczka

7

1 reference

Europe PubMed Central

24 June 2017

Mario Menschikowski

8

1 reference

Europe PubMed Central

24 June 2017

Gisela Stoltenburg-Didinger

9

1 reference

Europe PubMed Central

24 June 2017

Katrin Koehler

10

1 reference

Europe PubMed Central

24 June 2017

language of work or name

0 references

publication date

1 March 2006

1 reference

Europe PubMed Central

24 June 2017

Molecular and Cellular Biology

1 reference

Europe PubMed Central

24 June 2017

26

1 reference

Europe PubMed Central

24 June 2017

5

1 reference

Europe PubMed Central

24 June 2017

1879-1887

1 reference

Europe PubMed Central

24 June 2017

The triple A syndrome is due to mutations in ALADIN, a novel member of the nuclear pore complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

Proteomic analysis of the mammalian nuclear pore complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

Disruption of the FG nucleoporin NUP98 causes selective changes in nuclear pore complex stoichiometry and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

Triple A syndrome--clinical aspects and molecular genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

Mutant WD-repeat protein in triple-A syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

G2 arrest and impaired nucleocytoplasmic transport in mouse embryos lacking the proto-oncogene CAN/Nup214

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

17 March 2017

The nuclear pore complex: a jack of all trades?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

29 September 2017

The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

29 September 2017

Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

29 September 2017

ACTH resistance syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

29 September 2017

Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

29 September 2017

Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

29 September 2017

Disrupted compaction of CNS myelin in an OSP/Claudin-11 and PLP/DM20 double knockout mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

27 November 2018

Abnormal anxiety-related behavior in serotonin transporter null mutant mice: the influence of genetic background

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

27 November 2018

The use of behavioral test batteries: effects of training history.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430267

27 November 2018

Generation and analysis of interleukin-4 deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive observational assessment: Ia. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Drug effects on motor coordination

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucocorticoid and Partial Mineralocorticoid Deficiency Associated with Achalasia*

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Individual motor activity--relationships to dopaminergic responses

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenocorticotropin insensitivity syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16479006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.26.5.1879-1887.2006

1 reference

Europe PubMed Central

24 June 2017

0 references

1 reference

Europe PubMed Central

24 June 2017

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