Citations for
1STX7, UNC13D
Munc13-4 interacts with syntaxin 7 and regulates late endosomal maturation, endosomal signaling, and TLR9-initiated cellular responses.
He J, Johnson JL, Monfregola J, Ramadass M, Pestonjamasp K, Napolitano G, Zhang J, Catz SD.
Mol Biol Cell 27(3):572-87. doi: 10.1091/mbc.E15-05-0283. Epub 2015 Dec 17. 2016
2UNC13D
Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome.
Aricò M, Boggio E, Cetica V, Melensi M, Orilieri E, Clemente N, Cappellano G, Buttini S, Soluri MF, Comi C, Dufour C, Pende D, Dianzani I, Ellis SR, Pagliano S, Marcenaro S, Ramenghi U, Chiocchetti A, Dianzani U.
PLoS One 8(7):e68045. doi: 10.1371/journal.pone.0068045. Print 2013. 2013
3HPLH3, UNC13D
Defective UNC13D Gene-associated Familial Hemophagocytic Lymphohistiocytosis Triggered by Visceral Leishmaniasis: A Diagnostic Challenge.
Balta G, Azik FM, Gurgey A.
J Pediatr Hematol Oncol Pediatr Hematol Oncol. 2013 Jun 14. [Epub ahead of print] 2013
4HPLH3, UNC13D
Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3.
Entesarian M, Chiang SC, Schlums H, Meeths M, Chan MY, Mya SN, Soh SY, Nordenskjöld M, Henter JI, Bryceson YT.
Br J Haematol 162(3):415-8. doi: 10.1111/bjh.12371. Epub 2013 May 14. No abstract available. 2013
5RAB27A, UNC13D
MUNC13-4 protein regulates the oxidative response and is essential for phagosomal maturation and bacterial killing in neutrophils.
Monfregola J, Johnson JL, Meijler MM, Napolitano G, Catz SD.
J Biol Chem 287(53):44603-18. doi: 10.1074/jbc.M112.414029. Epub 2012 Oct 31. 2012
6UNC13D
Munc13-4 reconstitutes calcium-dependent SNARE-mediated membrane fusion.
Boswell KL, James DJ, Esquibel JM, Bruinsma S, Shirakawa R, Horiuchi H, Martin TF.
J Cell Biol 197(2):301-12. doi: 10.1083/jcb.201109132. 2012
7HPLH3, UNC13D
A novel Dutch mutation in UNC13D reveals an essential role of the C2B domain in munc13-4 function.
Elstak ED, te Loo M, Tesselaar K, van Kerkhof P, Loeffen J, Grivas D, Hennekam E, Boelens JJ, Hoogerbrugge PM, van der Sluijs P, van Gijn ME, van de Corput L.
Pediatr Blood Cancer 58(4):598-605. doi: 10.1002/pbc.23253. Epub 2011 Jul 13. 2012
8UNC13D
Munc13-4 restricts motility of Rab27a-expressing vesicles to facilitate lipopolysaccharide-induced priming of exocytosis in neutrophils.
Johnson JL, Hong H, Monfregola J, Kiosses WB, Catz SD.
J Biol Chem 286(7):5647-56. doi: 10.1074/jbc.M110.184762. Epub 2010 Dec 9. 2011
9HPLH2, HPLH3, HPLH5, PRF1, STXBP2, UNC13D
Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.
Zhang K, Jordan MB, Marsh RA, Johnson JA, Kissell D, Meller J, Villanueva J, Risma KA, Wei Q, Klein PS, Filipovich AH.
Blood 118(22):5794-8. doi: 10.1182/blood-2011-07-370148. Epub 2011 Aug 31. 2011
10UNC13D
Munc13-4 is a limiting factor in the pathway required for platelet granule release and hemostasis.
Ren Q, Wimmer C, Chicka MC, Ye S, Ren Y, Hughson FM, Whiteheart SW.
Blood 116(6):869-77. doi: 10.1182/blood-2010-02-270934. Epub 2010 Apr 30. 2010
11UNC13D, HPLH3
Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
Rudd E, Bryceson YT, Zheng C, Edner J, Wood SM, Ramme K, Gavhed S, GŸrgey A, Hellebostad M, Bechensteen AG, Ljunggren HG, Fadeel B, Nordenskjšld M, Henter JI.
J Med Genet 45(3):134-41. Epub 2007 Nov 9. 2008
12UNC13D, HPLH3
Genetic loci contributing to hemophagocytic lymphohistiocytosis do not confer susceptibility to systemic-onset juvenile idiopathic arthritis.
Donn R, Ellison S, Lamb R, Day T, Baildam E, Ramanan AV.
Arthritis Rheum 58(3):869-74. 2008
13HPLH2, HPLH3, HPLH4, PRF1, STX11, UNC13D
Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.
Horne A, Ramme KG, Rudd E, Zheng C, Wali Y, al-Lamki Z, Gürgey A, Yalman N, Nordenskjöld M, Henter JI.
Br J Haematol 143(1):75-83. Epub 2008 Aug 15. 2008
14DOC2A, UNC13D
Doc2 alpha and Munc13-4 regulate Ca(2+) -dependent secretory lysosome exocytosis in mast cells.
Higashio H, Nishimura N, Ishizaki H, Miyoshi J, Orita S, Sakane A, Sasaki T.
J Immunol 180(7):4774-84. 2008
15PRF1, HPLH2, UNC13D, HPLH3, RAB27A, VCIPD2, STX11, HPLH4
Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
Zur Stadt U, Beutel K, Kolberg S, Schneppenheim R, Kabisch H, Janka G, Hennies HC.
Hum Mutat 27(1):62-8. 2006
16UNC13D, HPLH3
Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes.
Yamamoto K, Ishii E, Sako M, Ohga S, Furuno K, Suzuki N, Ueda I, Imayoshi M, Yamamoto S, Morimoto A, Takada H, Hara T, Imashuku S, Sasazuki T, Yasukawa M.
J Med Genet 41(10):763-7. 2004
17UNC13D
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Feldmann J, Callebaut I, Raposo G, Certain S, Bacq D, Dumont C, Lambert N, Ouachee-Chardin M, Chedeville G, Tamary H, Minard-Colin V, Vilmer E, Blanche S, Le Deist F, Fischer A, de Saint Basile G.
Cell 115(4):461-73. 2003