MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells

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Craniofacial anomalies associated with hypospadias. Description of a hospital based population in South America.Clearance of a persistent picornavirus infection is associated with enhanced pro-apoptotic and cellular immune responses.

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Q38937792-170D91FC-F921-46A3-A69E-534C5E182E95 Q47563315-2F8BFBD3-AE7B-4046-8C1F-95A4C436A04D

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MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells

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http://www.wikidata.org/entity/Q56112082

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wetenschappelijk artikel

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наукова стаття, опублікована у квітні 2015

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MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

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MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

@nl

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Item

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MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

@en

MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

@nl

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MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

@en

MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

@nl

P1476

MID2 can substitute for MID1 a ...... granules in cytotoxic T cells

@en

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Ann K. Hansen

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

Germana Meroni

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

Lasse Boding

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

Niels Ødum

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

Trine B. Levring

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P2860

MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development

The tripartite motif family identifies cell compartments.

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4.

TRIM family proteins and their emerging roles in innate immunity

X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum

MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation

FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules.

Shouts, whispers and the kiss of death: directional secretion in T cells

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682-687

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scholarly article

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10.1111/APM.12402

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

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123

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Anders Woetmann

Carsten Geisler

Charlotte Menné Bonefeld

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2015-04-30T00:00:00Z

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25924778

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exocytosis

MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells

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MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921