Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality. - Wikidata - awgldk - TriplyDB

Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality.

Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality.

http://www.wikidata.org/entity/Q37560138

about

Response to letter to the editor of Carcinogenesis by Pira et al., 2017.A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.

P2860

Q46164705-B79A0C13-D61B-424A-AF48-8067AD78AFB3 Q48109687-E872B29E-E3D6-4742-96D9-F4B3F98B54EA

P2860

Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality.

http://www.wikidata.org/entity/Q37560138

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 26 October 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@en

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@nl

type

label

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@en

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@nl

prefLabel

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@en

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@nl

P1433

Q37560138-8D990E52-E910-4B80-8D16-CC578B276558

P1476

Q37560138-BE1A77D7-C258-4A5D-9B4C-A6C739B023D0

P2093

Q37560138-0F080623-F1D1-43B5-971D-BB5730E0FD96

Q37560138-2A311BDF-1C01-452A-A8C3-DE9AB6585C9D

Q37560138-74060AF8-631F-48E6-98C6-77B6DA1DC494

Q37560138-9C458F2F-2D0D-4039-A767-5A7CBF143D1B

Q37560138-A24EA3B2-4DAF-4682-9A30-F02A1D0FA09D

Q37560138-B147301C-3A52-4BE4-9B1B-3149499B7088

Q37560138-B9B4FD00-5A55-4BF4-9541-D10DD3267091

P2860

Q37560138-06BCA290-4257-4512-8B03-81AF15C8AB16

Q37560138-12646EFA-0072-4A4A-9D47-14ED49B04B02

Q37560138-14D68241-128B-4982-82FF-15FF0B80C759

Q37560138-19037447-C6A8-4A9E-A77E-D024B4527FD6

Q37560138-1B0259CA-548C-49F8-A63D-15D430AE7FAA

Q37560138-1B601619-3219-41FD-B34E-652110B0C75A

Q37560138-267BC497-CE7B-43D1-8B0C-C982227DB2B2

Q37560138-2C0334FA-8B49-45D5-AC52-ABFF1F4FCB44

Q37560138-2CB530E3-32CA-4065-9ED2-1BEA021C12BF

Q37560138-38D2E4EC-4A5A-4817-BD34-850696A2CEAA

P304

Q37560138-D3923E35-76DB-4DBC-8D25-70155ADBA4F0

P31

Q37560138-BB7795CB-43FE-458B-B91C-6FE969F34E48

P356

Q37560138-97FE6134-5CCC-4010-9856-A983E9831958

P407

Q37560138-A9E9862E-9813-4642-A5DB-45F9072BC267

P433

Q37560138-CA58ED3A-92BB-4EC5-BBD0-E720758A0274

P478

Q37560138-EB402A7E-D1C2-4805-98E6-F1E0B6F4D879

P50

Q37560138-1C077D49-A82C-48B8-BE1D-145ADB6B3553

Q37560138-3B1D6908-F2A7-4AD2-9DD9-E0BE4847E626

Q37560138-85434282-5252-470D-8D65-BC7C21519AB2

Q37560138-89C38ED2-19A8-4867-9C0D-4C723B708B0D

Q37560138-8A8D0DB3-585F-4837-85C2-C7C41C963CBA

Q37560138-A3723BE5-3420-4F40-9ED8-699539455A9C

Q37560138-E2F0633E-08E4-4E11-924F-6ADE6D5BEA00

Q37560138-E5737E56-4CD4-446E-B688-CE61813EDEE7

P577

Q37560138-98B08D16-68D9-4F79-B75F-BCA9762A0FFC

P698

Q37560138-070590DE-6AD9-4E23-8EFD-A8C1C31AD0E3

P932

Q37560138-3D164063-D4F6-4036-AE7A-DB065E8D5FF3

P356

0008-5472.CAN-16-1386

P1433

Cancer Research

P1476

Mutational Landscape and Gene ...... osomy 7 as a Sole Abnormality.

@en

P2093

Andrew J Carroll

http://www.w3.org/2001/XMLSchema#string

Ann-Kathrin Eisfeld

http://www.w3.org/2001/XMLSchema#string

Christopher Oakes

http://www.w3.org/2001/XMLSchema#string

Deedra Nicolet

http://www.w3.org/2001/XMLSchema#string

Karl Kroll

http://www.w3.org/2001/XMLSchema#string

Richard M Stone

http://www.w3.org/2001/XMLSchema#string

Shelley Orwick

http://www.w3.org/2001/XMLSchema#string

P2860

Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7

Mammalian SWI/SNF chromatin remodeling complexes and cancer: Mechanistic insights gained from human genomics

Regulation of development and cancer by the R2B subfamily of RPTPs and the implications of proteolysis

TET2 mutations improve the new European LeukemiaNet risk classification of acute myeloid leukemia: a Cancer and Leukemia Group B study.

TET2 mutation is an unfavorable prognostic factor in acute myeloid leukemia patients with intermediate-risk cytogenetics.

Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study

Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461)

Mutations predisposing to hereditary nonpolyposis colorectal cancer

Two transforming C-RAF germ-line mutations identified in patients with therapy-related acute myeloid leukemia

A framework for variation discovery and genotyping using next-generation DNA sequencing data

P304

207-218

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1158/0008-5472.CAN-16-1386

http://www.w3.org/2001/XMLSchema#string

P407

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

77

http://www.w3.org/2001/XMLSchema#string

P50

Stefano Volinia

Ann-Kathrin Eisfeld

Clara D. Bloomfield

James S Blachly

Albert de la Chapelle

Krzysztof Mrózek

Jessica Kohlschmidt

P577

2016-10-26T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27784745

http://www.w3.org/2001/XMLSchema#string

P932

5215102

http://www.w3.org/2001/XMLSchema#string