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Items: 16

1.

Genetic models reveal origin, persistence and non-redundant functions of IL-17-producing γδ T cells.

Sandrock I, Reinhardt A, Ravens S, Binz C, Wilharm A, Martins J, Oberdörfer L, Tan L, Lienenklaus S, Zhang B, Naumann R, Zhuang Y, Krueger A, Förster R, Prinz I.

J Exp Med. 2018 Dec 3;215(12):3006-3018. doi: 10.1084/jem.20181439. Epub 2018 Nov 19.

PMID:
30455268
2.

Publisher Correction: Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection.

Ravens S, Schultze-Florey C, Raha S, Sandrock I, Drenker M, Oberdörfer L, Reinhardt A, Ravens I, Beck M, Geffers R, von Kaisenberg C, Heuser M, Thol F, Ganser A, Förster R, Koenecke C, Prinz I.

Nat Immunol. 2018 Sep;19(9):1037. doi: 10.1038/s41590-018-0054-x.

PMID:
29449629
3.

Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection.

Ravens S, Schultze-Florey C, Raha S, Sandrock I, Drenker M, Oberdörfer L, Reinhardt A, Ravens I, Beck M, Geffers R, von Kaisenberg C, Heuser M, Thol F, Ganser A, Förster R, Koenecke C, Prinz I.

Nat Immunol. 2017 Apr;18(4):393-401. doi: 10.1038/ni.3686. Epub 2017 Feb 20. Erratum in: Nat Immunol. 2018 Feb 14;:.

PMID:
28218745
4.

Interleukin-23-Dependent γ/δ T Cells Produce Interleukin-17 and Accumulate in the Enthesis, Aortic Valve, and Ciliary Body in Mice.

Reinhardt A, Yevsa T, Worbs T, Lienenklaus S, Sandrock I, Oberdörfer L, Korn T, Weiss S, Förster R, Prinz I.

Arthritis Rheumatol. 2016 Oct;68(10):2476-86. doi: 10.1002/art.39732.

5.

MicroRNA-181a/b-1 Is Not Required for Innate γδ NKT Effector Cell Development.

Sandrock I, Ziętara N, Łyszkiewicz M, Oberdörfer L, Witzlau K, Krueger A, Prinz I.

PLoS One. 2015 Dec 16;10(12):e0145010. doi: 10.1371/journal.pone.0145010. eCollection 2015.

6.

γδ T cells come to stay: Innate skin memory in the Aldara model.

Prinz I, Sandrock I.

Eur J Immunol. 2015 Nov;45(11):2994-7. doi: 10.1002/eji.201546033. Epub 2015 Oct 12.

7.

A clonotypic Vγ4Jγ1/Vδ5Dδ2Jδ1 innate γδ T-cell population restricted to the CCR6⁺CD27⁻ subset.

Kashani E, Föhse L, Raha S, Sandrock I, Oberdörfer L, Koenecke C, Suerbaum S, Weiss S, Prinz I.

Nat Commun. 2015 Mar 13;6:6477. doi: 10.1038/ncomms7477.

PMID:
25765849
8.

Critical role for miR-181a/b-1 in agonist selection of invariant natural killer T cells.

Ziętara N, Łyszkiewicz M, Witzlau K, Naumann R, Hurwitz R, Langemeier J, Bohne J, Sandrock I, Ballmaier M, Weiss S, Prinz I, Krueger A.

Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7407-12. doi: 10.1073/pnas.1221984110. Epub 2013 Apr 15.

9.

Development of interleukin-17-producing γδ T cells is restricted to a functional embryonic wave.

Haas JD, Ravens S, Düber S, Sandrock I, Oberdörfer L, Kashani E, Chennupati V, Föhse L, Naumann R, Weiss S, Krueger A, Förster R, Prinz I.

Immunity. 2012 Jul 27;37(1):48-59. doi: 10.1016/j.immuni.2012.06.003. Epub 2012 Jul 5.

10.

Aberrant DNA methylation characterizes juvenile myelomonocytic leukemia with poor outcome.

Olk-Batz C, Poetsch AR, Nöllke P, Claus R, Zucknick M, Sandrock I, Witte T, Strahm B, Hasle H, Zecca M, Stary J, Bergstraesser E, De Moerloose B, Trebo M, van den Heuvel-Eibrink MM, Wojcik D, Locatelli F, Plass C, Niemeyer CM, Flotho C; European Working Group of Myelodysplastic Syndromes in Childhood (EWOG-MDS).

Blood. 2011 May 5;117(18):4871-80. doi: 10.1182/blood-2010-08-298968. Epub 2011 Mar 15.

11.

Methylation of the PTEN gene CpG island is infrequent in juvenile myelomonocytic leukemia: Comments on "PTEN deficiency is a common defect in juvenile myelomonocytic leukemia" [Leuk. Res. 2009;33:671-677 (Epub 2008 November 17)].

Batz C, Sandrock I, Niemeyer CM, Flotho C.

Leuk Res. 2009 Nov;33(11):1578-9; author reply 1580. doi: 10.1016/j.leukres.2009.04.040. Epub 2009 May 31. No abstract available.

PMID:
19487024
12.

The DNA methyltransferase inhibitors azacitidine, decitabine and zebularine exert differential effects on cancer gene expression in acute myeloid leukemia cells.

Flotho C, Claus R, Batz C, Schneider M, Sandrock I, Ihde S, Plass C, Niemeyer CM, Lübbert M.

Leukemia. 2009 Jun;23(6):1019-28. doi: 10.1038/leu.2008.397. Epub 2009 Feb 5.

PMID:
19194470
13.

Association of HAX1 deficiency with neurological disorder.

Rezaei N, Chavoshzadeh Z, R Alaei O, Sandrock I, Klein C.

Neuropediatrics. 2007 Oct;38(5):261-3. doi: 10.1055/s-2008-1062704.

PMID:
18330843
14.

Large granular lymphocyte proliferation and revertant mosaicism: two rare events in a Wiskott-Aldrich syndrome patient.

Boztug K, Baumann U, Ballmaier M, Webster D, Sandrock I, Jacobs R, Lion T, Preuner S, Germeshausen M, Hansen G, Welte K, Klein C.

Haematologica. 2007 Mar;92(3):e43-5.

15.

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Schäffer AA, Rathinam C, Boztug K, Schwinzer B, Rezaei N, Bohn G, Melin M, Carlsson G, Fadeel B, Dahl N, Palmblad J, Henter JI, Zeidler C, Grimbacher B, Welte K.

Nat Genet. 2007 Jan;39(1):86-92. Epub 2006 Dec 24.

PMID:
17187068
16.

Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2.

Jung J, Bohn G, Allroth A, Boztug K, Brandes G, Sandrock I, Schäffer AA, Rathinam C, Köllner I, Beger C, Schilke R, Welte K, Grimbacher B, Klein C.

Blood. 2006 Jul 1;108(1):362-9. Epub 2006 Mar 14.

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