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

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

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

http://www.wikidata.org/entity/Q28202423

about

sameAs

Nuclear translocation of integrin cytoplasmic domain-associated protein 1 stimulates cellular proliferation.Krit 1 interactions with microtubules and membranes are regulated by Rap1 and integrin cytoplasmic domain associated protein-1 Biomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis Mutations within the MGC4607 gene cause cerebral cavernous malformations CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis Cerebral cavernous malformation protein CCM1 inhibits sprouting angiogenesis by activating DELTA-NOTCH signaling.Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein.Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene Endothelial cell-cell adhesion during zebrafish vascular development Mechanism for KRIT1 Release of ICAP1-Mediated Suppression of Integrin Activation KRIT-1/CCM1 is a Rap1 effector that regulates endothelial cell cell junctions Identification of the Kelch family protein Nd1-L as a novel molecular interactor of KRIT1 Transient receptor potential family members PKD1L3 and PKD2L1 form a candidate sour taste receptor Structural basis for the disruption of the cerebral cavernous malformations 2 (CCM2) interaction with Krev interaction trapped 1 (KRIT1) by disease-associated mutations Pediatric cerebral cavernous malformations: Genetics, pathogenesis, and management.Phosphorylation sites in the cerebral cavernous malformations complex CCM1-ICAP-1 complex controls β1 integrin-dependent endothelial contractility and fibronectin remodeling Interaction-based feature selection and classification for high-dimensional biological data Defective osteoblast function in ICAP-1-deficient mice Cerebral cavernous malformation: new molecular and clinical insights.Recent insights into cerebral cavernous malformations: a complex jigsaw puzzle under construction.Cerebral cavernous malformations: somatic mutations in vascular endothelial cells Defining the functional domain of programmed cell death 10 through its interactions with phosphatidylinositol-3,4,5-trisphosphate.Role of cytoskeletal proteins in cerebral cavernous malformation signaling pathways: a proteomic analysis.Control of cell adhesion dynamics by Rap1 signaling.A mouse model of heritable cerebrovascular disease.Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology.Analysis of conserved residues in the betapat-3 cytoplasmic tail reveals important functions of integrin in multiple tissues.A mechanism of Rap1-induced stabilization of endothelial cell--cell junctions.Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations.ANKS1B Interacts with the Cerebral Cavernous Malformation Protein-1 and Controls Endothelial Permeability but Not Sprouting Angiogenesis.Heart of glass anchors Rasip1 at endothelial cell-cell junctions to support vascular integrity Role of Krev Interaction Trapped-1 in Prostacyclin-Induced Protection against Lung Vascular Permeability Induced by Excessive Mechanical Forces and Thrombin Receptor Activating Peptide 6.Roles for ROS and hydrogen sulfide in the longevity response to germline loss in Caenorhabditis elegans.Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis.Endogenous endothelial cell signaling systems maintain vascular stability.Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration.

P2860

Q24294613-4F1DF39A-F704-48C2-A23C-FAC26BF9721A Q24296474-4485F8A5-62A8-4E2B-BECA-6AF5E4A5D3A7 Q24302790-28C771E1-BFD2-4CFA-976C-BB7DCDDD266B Q24306080-45988642-4F86-44BF-A38E-2F6BD547A2D9 Q24309334-278A34A8-9E6A-491E-B8C3-DC5CB230DA2D Q24338286-81E7936B-A4FE-45A3-A471-D0A5717A8489 Q24530747-7BD785A9-0D87-41B6-93B2-543397DE6959 Q24532144-3FD4DF21-2009-4207-9DE3-2C5111E79A51 Q24532170-C2752088-68C3-4724-BC49-E7A735C783BF Q24533596-C866851A-8885-4E9D-8C18-0437071B64E8 Q24794976-6FC7BC68-92C9-43A1-819E-AA863F9BCFCE Q27005949-D8063D13-1B91-418C-B72A-6764CAA43758 Q27675893-D6B59D24-2557-4467-B613-0FAB0B57D3E8 Q28254336-F2128973-1029-427D-859C-1F2F8B78C443 Q28592808-4BE992D0-2A65-4E94-B197-C712746F52A7 Q28592962-15F62EFF-9B64-4C09-9736-EE86FF23510E Q28650470-4B743261-DACD-4B4B-B762-1505608D7769 Q30363436-D6B09F15-D801-49F4-969D-9240C0E3945E Q30423675-337619A8-F69F-4DA0-B80B-2C7933262FC3 Q30542261-1889F9CF-9850-4008-AE8A-209E94663319 Q30560970-2C72F110-B000-4788-8B2D-6DBA64846A18 Q33287597-5137A660-7DD0-4D01-A1A5-500FE2C97EE0 Q33342264-BBCCE372-5011-4961-8A91-6FF18F970DEC Q33348515-F18CA15D-F685-4496-B966-2B266922ED68 Q33477821-D454A85F-27CC-4D66-8FA0-CFBAEB9A809A Q33644309-7CC1FBA2-9BF7-4EB6-8E51-ABF526BB7865 Q33707224-14B68A3A-FEAC-45C3-B8CC-DD512FA6D188 Q33740476-159E92F9-3037-4186-8871-57AF2DC6D78B Q33789113-AB0092BD-9C17-4714-B594-B5768C1FF5AD Q34621267-FDC89B73-A3C9-44AC-AA3F-C0FACEA23647 Q34846048-A22A4CA1-90B2-4033-B2AE-41E99DEB44B3 Q35102621-1B3D940D-86AD-4C9E-8C54-7635B678C704 Q35103397-86CBC08A-6146-415F-9DEE-B42B4A1AB9F1 Q35876785-076DF6B1-3844-406D-93DB-441727F653B9 Q36520923-2C2058FC-E447-4B3A-BEC3-112550BFAFD2 Q36549093-1553920A-F596-4600-A77B-B0273A56A2FA Q36931039-4E5129EA-D529-40F6-8F20-4F2AD8817599 Q37092450-A270A288-A0FE-467A-ACBA-6B5C49396ED1 Q37231575-4D6AFF3F-09E3-4B6B-BA7D-5B0662DC39FA Q37618688-092CA2D5-76F0-43DA-B932-C064EEDCB0C7

P2860

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

http://www.wikidata.org/entity/Q28202423

description

2002 nî lūn-bûn

@nan

2002 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu

name

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@ast

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@en

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@nl

type

label

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@ast

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@en

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@nl

prefLabel

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@ast

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@en

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@nl

P1433

Q28202423-2469CE04-4F04-44E8-B4EA-2E8F98D67834

P1476

Q28202423-820DE94E-0945-4987-B363-2BAE53D4D576

P2093

Q28202423-48E133D6-B78D-40FC-B08C-7966D73A6FC7

Q28202423-6F009D42-A865-4EAC-A2D3-53D14AC5748B

Q28202423-D2A7C069-966A-4EE5-A245-E25B3C662048

Q28202423-D56C56C1-C23E-4876-A34C-3D20504E3816

Q28202423-DFBBB7A6-AF0A-40F1-92B8-C47A14AF5A0C

P304

Q28202423-A7259EC2-A7FE-4CD2-AA60-3C128F44707C

P31

Q28202423-3B104D48-DBA4-4C79-AD26-37894B9CB768

P3181

Q28202423-7563B4A7-B07B-472E-9F85-C48741176A44

P356

Q28202423-EC4C6BC1-B84A-4EDE-8F42-B314A7DCBE6E

P407

Q28202423-8C895C19-BFE6-4A4D-9998-AD76CAEAD6BD

P433

Q28202423-907C522B-E609-48E3-A493-F50D176DDC96

P478

Q28202423-D7E67E99-59F2-43CE-B42C-FE84C3CE0A1E

P577

Q28202423-F4E2567F-F5C4-4A86-B76E-329E16C7C6E2

P5875

Q28202423-EAC8B395-FB67-42E2-9DDD-76B8F1479390

P698

Q28202423-2ABA89B4-CB95-485C-A559-199FC5F4FB0D

P921

Q28202423-9ADB8450-F2B0-4FC9-9361-94694D470965

P3181

P356

P1433

Human Molecular Genetics

P1476

KRIT1 association with the int ...... formations (CCM1) pathogenesis

@en

P2093

Douglas A Marchuk

http://www.w3.org/2001/XMLSchema#string

Erica A Golemis

http://www.w3.org/2001/XMLSchema#string

Ilya G Serebriiskii

http://www.w3.org/2001/XMLSchema#string

Jon S Zawistowski

http://www.w3.org/2001/XMLSchema#string

Maximilian F Lee

http://www.w3.org/2001/XMLSchema#string

P304

389-96

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

3531296

http://www.w3.org/2001/XMLSchema#string

P356

10.1093/HMG/11.4.389

http://www.w3.org/2001/XMLSchema#string

P407

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

11

http://www.w3.org/2001/XMLSchema#string

P577

2002-02-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

277682779

http://www.w3.org/2001/XMLSchema#string

P698

11854171

http://www.w3.org/2001/XMLSchema#string

P921