Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 68

1.

Identification of CP77 as the third orthopoxvirus SAMD9 and SAMD9L inhibitor with a unique specificity for a rodent SAMD9L.

Zhang F, Meng X, Townsend MB, Satheshkumar PS, Xiang Y.

J Virol. 2019 Mar 27. pii: JVI.00225-19. doi: 10.1128/JVI.00225-19. [Epub ahead of print]

PMID:
30918078
2.

A novel SAMD9 variant identified in patient with MIRAGE syndrome: Further defining syndromic phenotype and review of previous cases.

Perisa MP, Rose MJ, Varga E, Kamboj MK, Spencer JD, Bajwa RPS.

Pediatr Blood Cancer. 2019 Mar 21:e27726. doi: 10.1002/pbc.27726. [Epub ahead of print]

PMID:
30900330
3.

Measles Virus-Based Treatments Trigger a Pro-inflammatory Cascade and a Distinctive Immunopeptidome in Glioblastoma.

Rajaraman S, Canjuga D, Ghosh M, Codrea MC, Sieger R, Wedekink F, Tatagiba M, Koch M, Lauer UM, Nahnsen S, Rammensee HG, Mühlebach MD, Stevanovic S, Tabatabai G.

Mol Ther Oncolytics. 2018 Dec 31;12:147-161. doi: 10.1016/j.omto.2018.12.010. eCollection 2019 Mar 29.

4.

SAMD9 is a (epi-) genetically regulated anti-inflammatory factor activated in RA patients.

He P, Wu LF, Bing PF, Xia W, Wang L, Xie FF, Lu X, Lei SF, Deng FY.

Mol Cell Biochem. 2019 Feb 4. doi: 10.1007/s11010-019-03499-7. [Epub ahead of print]

PMID:
30715670
5.
6.

SOX2 participates in spermatogenesis of Zhikong scallop Chlamys farreri.

Liang S, Liu D, Li X, Wei M, Yu X, Li Q, Ma H, Zhang Z, Qin Z.

Sci Rep. 2019 Jan 11;9(1):76. doi: 10.1038/s41598-018-35983-3.

7.

Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.

Csillag B, Ilencikova D, Meissl M, Webersinke G, Laccone F, Narumi S, Haas O, Duba HC.

Pediatr Blood Cancer. 2019 Apr;66(4):e27589. doi: 10.1002/pbc.27589. Epub 2018 Dec 19.

PMID:
30565860
8.

[Association between SAMD9/SAMD9L and hematological malignancies].

Narumi S, Hasegawa T.

Rinsho Ketsueki. 2018;59(11):2475-2480. doi: 10.11406/rinketsu.59.2475. Japanese.

PMID:
30531146
9.

MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.

Shima H, Hayashi M, Tachibana T, Oshiro M, Amano N, Ishii T, Haruna H, Igarashi M, Kon M, Fukuzawa R, Tanaka Y, Fukami M, Hasegawa T, Narumi S.

PLoS One. 2018 Nov 7;13(11):e0206184. doi: 10.1371/journal.pone.0206184. eCollection 2018.

10.

Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes.

Nagata Y, Narumi S, Guan Y, Przychodzen BP, Hirsch CM, Makishima H, Shima H, Aly M, Pastor V, Kuzmanovic T, Radivoyevitch T, Adema V, Awada H, Yoshida K, Li S, Sole F, Hanna R, Jha BK, LaFramboise T, Ogawa S, Sekeres MA, Wlodarski MW, Cammenga J, Maciejewski JP.

Blood. 2018 Nov 22;132(21):2309-2313. doi: 10.1182/blood-2017-05-787390. Epub 2018 Oct 15. No abstract available.

PMID:
30322869
11.

[Progress in research of the pathogenesis of childhood MDS/MPN].

Yoshida K.

Rinsho Ketsueki. 2018;59(10):2284-2289. doi: 10.11406/rinketsu.59.2284. Japanese.

PMID:
30305537
12.

Myelodysplastic syndromes in children.

Galaverna F, Ruggeri A, Locatelli F.

Curr Opin Oncol. 2018 Nov;30(6):402-408. doi: 10.1097/CCO.0000000000000488.

PMID:
30222640
13.

Human Host Range Restriction of the Vaccinia Virus C7/K1 Double Deletion Mutant Is Mediated by an Atypical Mode of Translation Inhibition.

Sivan G, Glushakow-Smith SG, Katsafanas GC, Americo JL, Moss B.

J Virol. 2018 Nov 12;92(23). pii: e01329-18. doi: 10.1128/JVI.01329-18. Print 2018 Dec 1.

PMID:
30209174
14.
15.

Monosomy 7 in Pediatric Myelodysplastic Syndromes.

Wlodarski MW, Sahoo SS, Niemeyer CM.

Hematol Oncol Clin North Am. 2018 Aug;32(4):729-743. doi: 10.1016/j.hoc.2018.04.007. Review.

PMID:
30047423
16.

Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes.

Wong JC, Bryant V, Lamprecht T, Ma J, Walsh M, Schwartz J, Del Pilar Alzamora M, Mullighan CG, Loh ML, Ribeiro R, Downing JR, Carroll WL, Davis J, Gold S, Rogers PC, Israels S, Yanofsky R, Shannon K, Klco JM.

JCI Insight. 2018 Jul 26;3(14). pii: 121086. doi: 10.1172/jci.insight.121086. eCollection 2018 Jul 26.

17.

Quantitative Proteomic Analysis of Cell Responses to Electroporation, a Classical Gene Delivery Approach.

Zhao M, Zhao D, Ma Y, Hu Z, Wei Z.

Proteomics. 2018 Aug;18(16):e1800127. doi: 10.1002/pmic.201800127. Epub 2018 Aug 6.

PMID:
30035351
18.

The enigma of monosomy 7.

Inaba T, Honda H, Matsui H.

Blood. 2018 Jun 28;131(26):2891-2898. doi: 10.1182/blood-2017-12-822262. Epub 2018 Apr 3. Review.

PMID:
29615405
19.

SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.

Davidsson J, Puschmann A, Tedgård U, Bryder D, Nilsson L, Cammenga J.

Leukemia. 2018 May;32(5):1106-1115. doi: 10.1038/s41375-018-0074-4. Epub 2018 Feb 25. Review.

20.

A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing.

Kim YM, Seo GH, Kim GH, Ko JM, Choi JH, Yoo HW.

BMC Med Genet. 2018 Mar 5;19(1):35. doi: 10.1186/s12881-018-0546-4.

Supplemental Content

Loading ...
Support Center