(Q35156173)

English

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

oligodendrocyte

1 reference

based on heuristic

inferred from title

author name string

David Cheishvili

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Paula Dietrich

2

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Channa Maayan

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Aviel Even

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Miguel Weil

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Ioannis Dragatsis

6

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Aharon Razin

7

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

language of work or name

0 references

publication date

23 April 2014

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

e94612

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

copyright license

Creative Commons Attribution 4.0 International

23 April 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Phosphatidylserine increases IKBKAP levels in a humanized knock-in IKBKAP mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

IKAP/Elp1 is required in vivo for neurogenesis and neuronal survival, but not for neural crest migration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Deletion of exon 20 of the Familial Dysautonomia gene Ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Expression of myelin genes: comparative analysis of Oli-neu and N20.1 oligodendroglial cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Chemical inducers and transcriptional markers of oligodendrocyte differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Central autonomic dysfunction with defective lacrimation; report of five cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Hereditary sensory and autonomic neuropathies: types II, III, and IV

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Elongator complex: how many roles does it play?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Functional genomic analysis of oligodendrocyte differentiation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Elevated levels of two tRNA species bypass the requirement for elongator complex in transcription and exocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Optic neuropathies in inherited metabolic disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Familial dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Human Elongator facilitates RNA polymerase II transcription through chromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Purification and characterization of the human elongator complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

CNS myelination and PLP gene dosage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Biology of oligodendrocyte and myelin in the mammalian central nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

The I kappa B kinase (IKK) complex is tripartite and contains IKK gamma but not IKAP as a regular component.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Oligodendrocyte lineage and the motor neuron connection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Myelin-associated glycoprotein binding to gangliosides. Structural specificity and functional implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Neuron-oligodendroglial interactions during central nervous system development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Lines of murine oligodendroglial precursor cells immortalized by an activated neu tyrosine kinase show distinct degrees of interaction with axons in vitro and in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

Spinal Cord Changes in Familial Dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

The Sural Nerve in Familial Dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

28 July 2018

In vivo analysis of kallikrein-related peptidase 6 (KLK6) function in oligodendrocyte development and the expression of myelin proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Neuroimaging supports central pathology in familial dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

The temporal profile of genomic responses and protein synthesis in ischemic tolerance of the rat brain induced by repeated hyperbaric oxygen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Transcription impairment and cell migration defects in elongator-depleted cells: implication for familial dysautonomia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Structure and function of the myelin proteins: current status and perspectives in relation to multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Elp1p, the yeast homolog of the FD disease syndrome protein, negatively regulates exocytosis independently of transcriptional elongation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Comparative analysis detects dependencies among the 5' splice-site positions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

A novel specific role for I kappa B kinase complex-associated protein in cytosolic stress signaling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Cloning, characterization, and genomic structure of the mouse Ikbkap gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Genomic organization and chromosomal localization of the mouse IKBKAP gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Familial dysautonomia is caused by mutations of the IKAP gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

IKAP is a scaffold protein of the IkappaB kinase complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Axonal swellings and degeneration in mice lacking the major proteolipid of myelin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Evidence that the homeodomain protein Gtx is involved in the regulation of oligodendrocyte myelination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3997429

27 September 2018

Elongator, a Multisubunit Component of a Novel RNA Polymerase II Holoenzyme for Transcriptional Elongation

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0094612

21 January 2018

Incidence of familial dysautonomia in Israel 1977-1981

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative studies of dorsal root ganglia and neuropathologic observations on spinal cords in familial dysautonomia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ApoD, a glia-derived apolipoprotein, is required for peripheral nerve functional integrity and a timely response to injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial dysautonomia in a non-Jewish girl, with histological evidence of progression in the sural nerve

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative sensory testing of thermal and vibratory perception in familial dysautonomia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The re-expression of the homeodomain transcription factor Gtx during remyelination of experimentally induced demyelinating lesions in young and old rat brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Optic neuropathy in familial dysautonomia

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peripheral nerve abnormalities in the Riley-Day syndrome. Findings in a sural nerve biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IKAP localizes to membrane ruffles with filamin A and regulates actin cytoskeleton organization and cell migration

1 reference

https://pubmed.ncbi.nlm.nih.gov/24760006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0094612

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

2014PLoSO...994612C

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

ResearchGate publication ID

0 references

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