Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
about
Mst1 and Mst2 kinases: regulations and diseasesMst1 directs Myosin IIa partitioning of low and higher affinity integrins during T cell migrationPrimary immunodeficiency update: Part I. Syndromes associated with eczematous dermatitisMST1-dependent vesicle trafficking regulates neutrophil transmigration through the vascular basement membraneEarly-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency.The transmembrane channel-like protein family and human papillomaviruses: Insights into epidermodysplasia verruciformis and progression to squamous cell carcinoma.MST1/MST2 Protein Kinases: Regulation and Physiologic Roles.Primary immunodeficiencies underlying fungal infectionsCompound heterozygous CORO1A mutations in siblings with a mucocutaneous-immunodeficiency syndrome of epidermodysplasia verruciformis-HPV, molluscum contagiosum and granulomatous tuberculoid leprosy.STK4 regulates TLR pathways and protects against chronic inflammation-related hepatocellular carcinoma.Partial defects of T-cell development associated with poor T-cell function.EVER2 deficiency is associated with mild T-cell abnormalities.Mycobacterium tuberculosis-triggered Hippo pathway orchestrates CXCL1/2 expression to modulate host immune responses.Cytokine immunomodulation for the treatment of infectious diseases: lessons from primary immunodeficiencies.Human Beta-papillomavirus infection and keratinocyte carcinomas.The non-canonical Hippo/Mst pathway in lymphocyte development and functions.Model systems of human papillomavirus-associated disease.Severe Epstein-Barr virus infection in primary immunodeficiency and the normal host.Mst1 Kinase Regulates the Actin-Bundling Protein L-Plastin To Promote T Cell Migration.Identification of LCK mutation in a family with atypical epidermodysplasia verruciformis with T-cell defects and virus-induced squamous cell carcinoma.Successful Curative Therapy With Rituximab and Allogeneic Haematopoietic Stem Cell Transplantation for MALT Lymphoma Associated With STK4-Mutated CD4+ Lymphocytopenia.The genetic basis of seborrhoeic dermatitis: a review.Expanding genetics and phenotypic spectrum of epidermodysplasia verruciformis.The Hippo Pathway: Immunity and Cancer.Primary atopic disorders.YAP/TAZ Activation as a Target for Treating Metastatic Cancer.Epidermodysplasia Verruciformis: Inborn Errors of Immunity to Human Beta-Papillomaviruses.CDG: An Online Server for Detecting Biologically Closest Disease-Causing Genes and its Application to Primary Immunodeficiency.EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency
P2860
Q22001145-B6073100-F5CE-4E33-ACCA-8D7F9C803BD5Q27313904-65BCA3FF-3FDD-49C9-BFD3-28860F997ABDQ28086897-007D9817-65D7-4CCA-95DD-6B9B452F9590Q30827642-F0BD334A-2335-4A97-9FB7-822B6AC9E5E4Q33418786-89142517-D538-48DC-9F68-DA10611ABC12Q33553561-CECC686D-226D-44DB-86C2-4951C4E590D4Q33821181-1B74595B-88BE-427C-AF0B-BBB5AF597F6CQ33902831-A976E268-949E-4D90-822D-5B449710DBB4Q35284909-9B50B14C-0AC1-4515-B0F1-4D1C03065C55Q36266490-E1C14FD6-ECF8-43D8-AF5D-028C66AD3878Q36808097-A25B6F09-1861-4E1E-8788-732CE8443405Q37069081-110BD3B3-4153-4DAC-9BCE-06DB30205450Q37435081-80CF676F-5AA4-494A-8851-3DEBD18FE32CQ38216460-3B68076C-2159-47B2-825B-61FF47D01FEEQ38240647-075F3FA9-148C-4E02-BB52-08EC031551C2Q38285449-3D49C359-5A92-4847-8486-FC6583154CF7Q38604326-359AA658-11AA-4336-BF75-FE5277024EC3Q38982455-366878FF-EB69-4B75-A7E4-A916D8DF201CQ40597463-0833C7E1-19BB-47BF-90CB-D61BDFC3E663Q40710875-22A0B364-DCD0-4604-B999-4AA259F15770Q40761804-61712AD9-2123-4506-A627-178B803A6B9DQ47387957-EC9DCF45-404A-420A-A9A2-A6ADF9C4C4D6Q47954424-CD959044-108D-4583-A16E-960F3BE0FBCDQ52621407-ED2537A8-854D-47B6-BF9E-F098C414557FQ52651330-C6FB6C2C-31FC-4876-8570-039C601DDF68Q54977387-2CA34B36-2B42-4C5F-98FF-D627B255739CQ55346681-6B6D41F1-7B40-4545-BFD2-58BFE8DCFDA5Q55620630-D587A978-B320-4BFE-A4C2-99EA9B015805Q58553724-BCE3E5AC-9AFC-4A54-8A65-DA6DF1CD3F0A
P2860
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
description
2012 nî lūn-bûn
@nan
2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@ast
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@en
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@nl
type
label
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@ast
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@en
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@nl
prefLabel
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@ast
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@en
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@nl
P2093
P2860
P50
P1433
P1476
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
@en
P2093
Amandine Crequer
Aurelia D'Amico
Avinash Abhyankar
Geneviève de Saint-Basile
Gérard Orth
Martine Munzer
P2860
P304
P356
10.1371/JOURNAL.PONE.0044010
P407
P50
P577
2012-08-27T00:00:00Z