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出版物地质文摘英文(3)	Springer电子图书(4326)	NATURE电子期刊(5625)	ACS电子期刊(17630)
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在“Wiley电子期刊”中，命中：1,510条，耗时：小于0.01 秒

在所有数据库中总计命中：755,413条

1.Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4

作者：Tobias Herold ; Klaus H. Metzeler ; Sebastian Vosberg ; Luise Hartmann ; Vindi Jurinovic ; Sabrina Opatz ; Nikola P. Konstandin ; Stephanie Schneider ; Evelyn Zellmeier ; Bianka Ksienzyk ; Alexander Graf ; Stefan Krebs ; Helmut Blum ; Maria Cristina Sauerland ; Thomas Bü ; chner ; Wolfgang E. Berdel ; Bernhard J. Wö ; rmann ; Ulrich Mansmann ; Wolfgang Hiddemann ; Stefan K. Bohlander ; Karsten Spiekermann and Philipp A. Greif

刊名：Genes, Chromosomes and Cancer

出版年：2017

2.METTL14 suppresses the metastatic potential of hepatocellular carcinoma by modulating N⁶‐methyladenosine‐dependent primary MicroRNA processing

作者：Jin‐zhao Ma ; Fu Yang ; Chuan‐chuan Zhou ; Feng Liu ; Ji‐hang Yuan ; Fang Wang ; Tian‐tian Wang ; Qing‐guo Xu ; Wei‐ping Zhou ; Shu‐han Sun

刊名：Hepatology

出版年：2017

3.Participation of TLR2 and TLR4 in Cytokines Production by Patients with Symptomatic and Asymptomatic Chronic Chagas Disease

作者：L. D. Mendes da Silva ; M. Gatto ; M. Miziara de Abreu Teodoro ; M. de Assis Golim ; &Eacute ; . A. Pelisson Nunes da Costa ; F. Capel Tavares Carvalho ; D. Ramos Rodrigues ; P. Câ ; mara Marques Pereira ; Â ; . M. Victoriano de Campos Soares and S. A. Calvi

刊名：Scandinavian Journal of Immunology

出版年：2017

4.KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connection

作者：Lauren Badalato ; Sali M. K. Farhan ; Allison A. Dilliott ; Care4Rare Canada Consortium ; Dennis E. Bulman ; Robert A. Hegele and Sharan L. Goobie

刊名：American Journal of Medical Genetics Part A

出版年：2017

5.Poor outcomes associated with +der(22)t(9;22) and −9/9p in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia receiving chemotherapy plus a tyrosine kinase inhibitor

作者：Nicholas J. Short ; Hagop M. Kantarjian ; Koji Sasaki ; Farhad Ravandi ; Heidi Ko ; C. Cameron Yin ; Guillermo Garcia-Manero ; Jorge E. Cortes ; Rebecca Garris ; Susan M. O'Brien ; Keyur Patel ; Maria Khouri ; Deborah Thomas ; Nitin Jain ; Tapan M. Kadia ; Naval G. Daver ; Christopher B. Benton ; Ghayas C. Issa ; Marina Konopleva and Elias Jabbour

刊名：American Journal of Hematology

出版年：2017

6.Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene

作者：Lucia Nacci ; Roberto Valli ; Rita Maria Pinto ; Marco Zecca ; Marco Cipolli ; Jacopo Morini ; Simone Cesaro ; Emanuela Boveri ; Vittorio Rosti ; Paola Corti ; Maura Ambroni ; Francesco Pasquali ; Cesare Danesino ; Emanuela Maserati and Antonella Minelli

刊名：Genes, Chromosomes and Cancer

出版年：2017

7.GATA3 expression in primary vulvar Paget disease: a potential pitfall leading to misdiagnosis of pagetoid urothelial intraepithelial neoplasia

作者：Diogo Morbeck ; Aline C Tregnago ; Glauco Baiocchi Netto ; Carlos Sacomani ; Patricia M Peresi ; Cynthia T Os&oacute ; rio ; Luciana Schutz ; Stephania M Bezerra ; Louise de Brot and Isabela W Cunha

刊名：Histopathology

出版年：2017

8.A de novo missense mutation in the inositol 1,4,5-triphosphate receptor type 1 gene causing severe pontine and cerebellar hypoplasia: Expanding the phenotype of ITPR1-related spinocerebellar ataxia's

作者：Tessa van Dijk ; Peter Barth ; Liesbeth Reneman ; Bart Appelhof ; Frank Baas and Bwee Tien Poll-The

刊名：American Journal of Medical Genetics Part A

出版年：2017

9.FOXP1 is a regulator of quiescence in healthy human CD4⁺ T cells and is constitutively repressed in T cells from patients with lymphoproliferative disorders

作者：Soizic Garaud ; Florence Roufosse ; Pushpamali De Silva ; Chunyan Gu-Trantien ; Jean-Nicolas Lodewyckx ; Hugues Duvillier ; Sarah Dedeurwaerder ; Martin Bizet ; Matthieu Defrance ; Franç ; ois Fuks ; Franç ; oise Bex and Karen Willard-Gallo

刊名：European Journal of Immunology

出版年：2017

10.Identification of C12orf4 as a gene for autosomal recessive intellectual disability

作者：A.K. Philips ; M. Pinelli ; C.I. de Bie ; A. Mustonen ; T. Mä ; ä ; ttä ; H.H. Arts ; K. Wu ; R. Roepman ; J.S. Moilanen ; S. Raza ; T. Varilo ; G. Scala ; S. Cocozza ; C. Gilissen ; K.L.I. van Gassen and I. Jä ; rvelä

刊名：Clinical Genetics

出版年：2017

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