Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 protein (Q39860393)

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scientific article published on June 2009

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English	Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 protein	scientific article published on June 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 protein (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

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Programmed cell death 10b

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GOA release 2020-03-11

Programmed cell death 10a

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GOA release 2020-03-11

cerebral cavernous malformation 3

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inferred from title

Benjamin M Hogan

3

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author name string

Katrin Voss

1

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Europe PubMed Central

PubMed publication ID

15 September 2017

Sonja Stahl

2

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Europe PubMed Central

PubMed publication ID

15 September 2017

Joerg Reinders

4

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Europe PubMed Central

PubMed publication ID

15 September 2017

Elisa Schleider

5

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Europe PubMed Central

PubMed publication ID

15 September 2017

Stefan Schulte-Merker

6

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Europe PubMed Central

PubMed publication ID

15 September 2017

Ute Felbor

7

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Europe PubMed Central

PubMed publication ID

15 September 2017

language of work or name

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publication date

1 June 2009

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Europe PubMed Central

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15 September 2017

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Europe PubMed Central

PubMed publication ID

15 September 2017

30

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Europe PubMed Central

PubMed publication ID

15 September 2017

6

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Europe PubMed Central

PubMed publication ID

15 September 2017

1003-1011

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Europe PubMed Central

PubMed publication ID

15 September 2017

Interaction between krit1 and malcavernin: implications for the pathogenesis of cerebral cavernous malformations.

1 reference

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21 January 2018

Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis

1 reference

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7 January 2021

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Krit 1 interactions with microtubules and membranes are regulated by Rap1 and integrin cytoplasmic domain associated protein-1

1 reference

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7 January 2021

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Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations

1 reference

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7 January 2021

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Zebrafish VEGF receptors: a guideline to nomenclature

1 reference

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7 January 2021

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Cloning of MASK, a novel member of the mammalian germinal center kinase III subfamily, with apoptosis-inducing properties

1 reference

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7 January 2021

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Large-scale mapping of human protein-protein interactions by mass spectrometry

1 reference

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7 January 2021

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Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion.

1 reference

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7 January 2021

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KRIT-1/CCM1 is a Rap1 effector that regulates endothelial cell cell junctions

1 reference

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A PP2A phosphatase high density interaction network identifies a novel striatin-interacting phosphatase and kinase complex linked to the cerebral cavernous malformation 3 (CCM3) protein

1 reference

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7 January 2021

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Mutations in apoptosis-related gene, PDCD10, cause cerebral cavernous malformation 3.

1 reference

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7 January 2021

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Proteomic identification of the cerebral cavernous malformation signaling complex

1 reference

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Caspase activation of mammalian sterile 20-like kinase 3 (Mst3). Nuclear translocation and induction of apoptosis

1 reference

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Cellular and molecular analyses of vascular tube and lumen formation in zebrafish.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

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A transgene-assisted genetic screen identifies essential regulators of vascular development in vertebrate embryos

1 reference

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7 January 2021

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Regulation of cardiovascular development and integrity by the heart of glass-cerebral cavernous malformation protein pathway

1 reference

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Genetics of cavernous angiomas

1 reference

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Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus

1 reference

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Deletions in CCM2 are a common cause of cerebral cavernous malformations

1 reference

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7 January 2021

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Inhibition of cell migration by autophosphorylated mammalian sterile 20-like kinase 3 (MST3) involves paxillin and protein-tyrosine phosphatase-PEST

1 reference

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7 January 2021

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PDCD10 interacts with Ste20-related kinase MST4 to promote cell growth and transformation via modulation of the ERK pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

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santa and valentine pattern concentric growth of cardiac myocardium in the zebrafish

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

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Cell motility: Golgi signalling shapes up to ship out.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

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SOK1 translocates from the Golgi to the nucleus upon chemical anoxia and induces apoptotic cell death.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

based on heuristic

inferred from DOI database lookup

A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

based on heuristic

inferred from DOI database lookup

YSK1 is activated by the Golgi matrix protein GM130 and plays a role in cell migration through its substrate 14-3-3zeta

1 reference

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7 January 2021

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Profiling phosphoproteins of yeast mitochondria reveals a role of phosphorylation in assembly of the ATP synthase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

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Cerebral cavernous malformation: new molecular and clinical insights

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

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Towards a proteome-scale map of the human protein–protein interaction network

1 reference

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7 January 2021

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Cloning and characterization of a human STE20-like protein kinase with unusual cofactor requirements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteome analysis of Apis mellifera royal jelly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20996

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex

1 reference

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7 January 2021

based on heuristic

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Rac-MEKK3-MKK3 scaffolding for p38 MAPK activation during hyperosmotic shock.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

CCM3 mutations are uncommon in cerebral cavernous malformations

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

The cerebral cavernous malformation signaling pathway promotes vascular integrity via Rho GTPases

1 reference

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7 January 2021

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inferred from DOI database lookup

Recognizing and defining true Ras binding domains I: biochemical analysis

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7 January 2021

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KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesis

1 reference

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inferred from DOI database lookup

CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis

1 reference

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Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation

1 reference

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7 January 2021

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Identifiers

10.1002/HUMU.20996

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

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