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Items: 1 to 20 of 79

1.

SM protein Munc18-2 facilitates transition of Syntaxin 11-mediated lipid mixing to complete fusion for T-lymphocyte cytotoxicity.

Spessott WA, Sanmillan ML, McCormick ME, Kulkarni VV, Giraudo CG.

Proc Natl Acad Sci U S A. 2017 Mar 14;114(11):E2176-E2185. doi: 10.1073/pnas.1617981114. Epub 2017 Mar 6.

PMID:
28265073
2.

Hemophagocytic Lymphohistiocytosis in Children: Pathogenesis and Treatment.

Ishii E.

Front Pediatr. 2016 May 13;4:47. doi: 10.3389/fped.2016.00047. eCollection 2016 May 13. Review.

3.

Comparison of Th1/Th2 cytokine profiles between primary and secondary haemophagocytic lymphohistiocytosis.

Chen Y, Wang Z, Luo Z, Zhao N, Yang S, Tang Y.

Ital J Pediatr. 2016 May 21;42(1):50. doi: 10.1186/s13052-016-0262-7.

4.

Approaches to Investigating Complex Genetic Traits in a Large-Scale Inbred Mouse Aging Study.

Sundberg JP, Berndt A, Sundberg BA, Silva KA, Kennedy V, Smith RS, Cooper TK, Schofield PN.

Vet Pathol. 2016 Mar;53(2):456-67. doi: 10.1177/0300985815612556.

5.

Munc18-2 is required for Syntaxin 11 Localization on the Plasma Membrane in Cytotoxic T-Lymphocytes.

Dieckmann NM, Hackmann Y, Aricò M, Griffiths GM.

Traffic. 2015 Dec;16(12):1330-41. doi: 10.1111/tra.12337. Epub 2015 Nov 2.

6.

A Novel Syntaxin 11 Gene (STX11) Mutation c.650T>C, p.Leu217Pro, in a Korean Child With Familial Hemophagocytic Lymphohistiocytosis.

Sultanova AK, Kim SK, Lee JW, Jang PS, Chung NG, Cho B, Park J, Kim Y, Kim M.

Ann Lab Med. 2016 Mar;36(2):170-3. doi: 10.3343/alm.2016.36.2.170.

7.

Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.

Tesi B, Lagerstedt-Robinson K, Chiang SC, Ben Bdira E, Abboud M, Belen B, Devecioglu O, Fadoo Z, Yeoh AE, Erichsen HC, Möttönen M, Akar HH, Hästbacka J, Kaya Z, Nunes S, Patiroglu T, Sabel M, Saribeyoglu ET, Tvedt TH, Unal E, Unal S, Unuvar A, Meeths M, Henter JI, Nordenskjöld M, Bryceson YT.

Genome Med. 2015 Dec 18;7:130. doi: 10.1186/s13073-015-0244-1.

8.

Cytotoxic granule secretion by lymphocytes and its link to immune homeostasis.

de Saint Basile G, Sepulveda FE, Maschalidi S, Fischer A.

F1000Res. 2015 Sep 30;4(F1000 Faculty Rev):930. doi: 10.12688/f1000research.6754.1. eCollection 2015 Sep 30. Review.

9.

Screening assays for primary haemophagocytic lymphohistiocytosis in children presenting with suspected macrophage activation syndrome.

Cruikshank M, Anoop P, Nikolajeva O, Rao A, Rao K, Gilmour K, Eleftheriou D, Brogan PA.

Pediatr Rheumatol Online J. 2015 Nov 16;12 Suppl 1:48. doi: 10.1186/s12969-015-0043-7.

10.

Hemophagocytic lymphohistiocytosis diagnosed by brain biopsy.

Ju HY, Hong CR, Kim SJ, Lee JW, Kim H, Kang HJ, Park KD, Shin HY, Chae JH, Phi JH, Cheon JE, Park SH, Ahn HS.

Korean J Pediatr. 2015 Sep;58(9):358-61. doi: 10.3345/kjp.2015.58.9.358. Epub 2015 Sep 21.

11.

Hemophagocytic syndrome: a dilemma chasing the intensivists.

Queiroz AF, Benevides GN, Fernandes Ide C, Goes Pde F, Bousso A, Ferreira CR.

Autops Case Rep. 2015 Mar 30;5(1):11-9. doi: 10.4322/acr.2014.044. eCollection 2015 Mar 30.

12.

Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry.

Cetica V, Sieni E, Pende D, Danesino C, De Fusco C, Locatelli F, Micalizzi C, Putti MC, Biondi A, Fagioli F, Moretta L, Griffiths GM, Luzzatto L, Aricò M.

J Allergy Clin Immunol. 2016 Jan;137(1):188-96.e4. doi: 10.1016/j.jaci.2015.06.048. Epub 2015 Sep 2.

13.

STX11 functions as a novel tumor suppressor gene in peripheral T-cell lymphomas.

Yoshida N, Tsuzuki S, Karube K, Takahara T, Suguro M, Miyoshi H, Nishikori M, Shimoyama M, Tsukasaki K, Ohshima K, Seto M.

Cancer Sci. 2015 Oct;106(10):1455-62. doi: 10.1111/cas.12742. Epub 2015 Aug 13.

14.

VAMP8-dependent fusion of recycling endosomes with the plasma membrane facilitates T lymphocyte cytotoxicity.

Marshall MR, Pattu V, Halimani M, Maier-Peuschel M, Müller ML, Becherer U, Hong W, Hoth M, Tschernig T, Bryceson YT, Rettig J.

J Cell Biol. 2015 Jul 6;210(1):135-51. doi: 10.1083/jcb.201411093. Epub 2015 Jun 29.

15.

An Emerging Role for SNARE Proteins in Dendritic Cell Function.

Collins LE, DeCourcey J, Soledad di Luca M, Rochfort KD, Loscher CE.

Front Immunol. 2015 Mar 31;6:133. doi: 10.3389/fimmu.2015.00133. eCollection 2015 Mar 31. Review.

16.

Hemophagocytic lymphohistiocytosis caused by dominant-negative mutations in STXBP2 that inhibit SNARE-mediated membrane fusion.

Spessott WA, Sanmillan ML, McCormick ME, Patel N, Villanueva J, Zhang K, Nichols KE, Giraudo CG.

Blood. 2015 Mar 5;125(10):1566-77. doi: 10.1182/blood-2014-11-610816. Epub 2015 Jan 6.

17.

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding.

Cetica V, Hackmann Y, Grieve S, Sieni E, Ciambotti B, Coniglio ML, Pende D, Gilmour K, Romagnoli P, Griffiths GM, Aricò M.

J Allergy Clin Immunol. 2015 May;135(5):1310-8.e1. doi: 10.1016/j.jaci.2014.08.039. Epub 2014 Oct 11.

18.

Genetic features of late onset primary hemophagocytic lymphohistiocytosis in adolescence or adulthood.

Wang Y, Wang Z, Zhang J, Wei Q, Tang R, Qi J, Li L, Ye L, Wang J, Ye L.

PLoS One. 2014 Sep 18;9(9):e107386. doi: 10.1371/journal.pone.0107386. eCollection 2014 Sep 18.

19.

The biogenesis of lysosomes and lysosome-related organelles.

Luzio JP, Hackmann Y, Dieckmann NM, Griffiths GM.

Cold Spring Harb Perspect Biol. 2014 Sep 2;6(9):a016840. doi: 10.1101/cshperspect.a016840. Review.

20.

Whole-exome sequencing reveals overlap between macrophage activation syndrome in systemic juvenile idiopathic arthritis and familial hemophagocytic lymphohistiocytosis.

Kaufman KM, Linghu B, Szustakowski JD, Husami A, Yang F, Zhang K, Filipovich AH, Fall N, Harley JB, Nirmala NR, Grom AA.

Arthritis Rheumatol. 2014 Dec;66(12):3486-95. doi: 10.1002/art.38793.

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