Cargando…

PB1819: KMT2A::ARHGEF12 RARE FUSION ASSOCIATED WITH A NOVEL GERMLINE DDX41 VARIANT IN ACUTE MYELOID LEUKEMIA

Detalles Bibliográficos
Autores principales:	Roubinet, Maxime, Rizzo, David, Chauzeix, Jasmine, Turlure, Pascal, Laforet, Marie-Pierre, Derouault, Paco, Feuillard, Jean, Yardin, Catherine, Auboiroux, Marie-Mathilde, Veyrune, Léa, Perani, Alexandre, Bourthoumieu, Sylvie, Dauriat, Benjamin, Gachard, Nathalie
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2023
Materias:	Publication Only
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430132/ http://dx.doi.org/10.1097/01.HS9.0000974124.17383.7c

Ejemplares similares

Hereditary predisposition to malignant myeloid hemopathies: Caution in use of saliva and guideline based on our experience
por: Perani, Alexandre, et al.
Publicado: (2023)

Normal serum protein electrophoresis and mutated IGHV genes detect very slowly evolving chronic lymphocytic leukemia patients
por: Chauzeix, Jasmine, et al.
Publicado: (2018)

CovCopCan: An efficient tool to detect Copy Number Variation from amplicon sequencing data in inherited diseases and cancer
por: Derouault, Paco, et al.
Publicado: (2020)

Clinical features of homozygous FIG4‐p.Ile41Thr Charcot‐Marie‐Tooth 4J patients
por: Lafontaine, Maxime, et al.
Publicado: (2021)

A reduced panel of eight genes (ATM, SF3B1, NOTCH1, BIRC3, XPO1, MYD88, TNFAIP3, and TP53) as an estimator of the tumor mutational burden in chronic lymphocytic leukemia
por: Chauzeix, Jasmine, et al.
Publicado: (2020)

DDX41-associated susceptibility to myeloid neoplasms
por: Makishima, Hideki, et al.
Publicado: (2023)

The emerging roles of the DDX41 protein in immunity and diseases
por: Jiang, Yan, et al.
Publicado: (2016)

Current Understanding of DDX41 Mutations in Myeloid Neoplasms
por: Kim, Kunhwa, et al.
Publicado: (2023)

New structural variations responsible for Charcot-Marie-Tooth disease: The first two large KIF5A deletions detected by CovCopCan software
por: Pyromali, Ioanna, et al.
Publicado: (2021)

Structural and functional analyses of human DDX41 DEAD domain
por: Jiang, Yan, et al.
Publicado: (2016)

A novel t(3;13)(q13;q12) translocation fusing FLT3 with GOLGB1: toward myeloid/lymphoid neoplasms with eosinophilia and rearrangement of FLT3?
por: Troadec, E, et al.
Publicado: (2017)

Erratum to: Structural and functional analyses of human DDX41 DEAD domain
por: Jiang, Yan, et al.
Publicado: (2017)

Are DDX41 variants of unknown significance and pathogenic variants created equal?
por: Xie, Zhuoer, et al.
Publicado: (2023)

DDX41 is needed for pre- and postnatal hematopoietic stem cell differentiation in mice
por: Ma, Jing, et al.
Publicado: (2022)

Observation and treatment in DDX41-mutated acute myeloid leukemia and myelodysplastic syndrome
por: Al-Kali, Aref, et al.
Publicado: (2023)

Ddx41 inhibition of DNA damage signaling permits erythroid progenitor expansion in zebrafish
por: Weinreb, Joshua T., et al.
Publicado: (2021)

DDX41 regulates the expression and alternative splicing of genes involved in tumorigenesis and immune response
por: Qin, Kai, et al.
Publicado: (2021)

DDX41 is required for cGAS-STING activation against DNA virus infection
por: Singh, Ravi Shankar, et al.
Publicado: (2022)

P442: DDX41 GERMLINE VARIANTS: POPULATION PREVALENCE, SIGNIFICANCE AND LEUKEMIC EVOLUTION
por: Cheloor Kovilakam, Sruthi, et al.
Publicado: (2023)

Circo, maroma y teatro, 1819-1910 /
por: Reyes de la Maza, Luis
Publicado: (1985)

Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia
por: Cardoso, S R, et al.
Publicado: (2016)

Structural and Functional Analysis of DDX41: a bispecific immune receptor for DNA and cyclic dinucleotide
por: Omura, Hiroki, et al.
Publicado: (2016)

Genetic features and clinical outcomes of patients with isolated and comutated DDX41-mutated myeloid neoplasms
por: Alkhateeb, Hassan B., et al.
Publicado: (2022)

Next-Generation Sequencing of DDX41 in Myeloid Neoplasms Leads to Increased Detection of Germline Alterations
por: Bannon, Sarah A., et al.
Publicado: (2021)

Outcomes of allogeneic transplant in patients with DDX41 mutated myelodysplastic syndrome and acute myeloid leukemia
por: Baranwal, Anmol, et al.
Publicado: (2022)

Unique role of DDX41, a DEAD-box type RNA helicase, in hematopoiesis and leukemogenesis
por: Shinriki, Satoru, et al.
Publicado: (2022)

Clinical and molecular correlates of somatic and germline DDX41 variants in patients and families with myeloid neoplasms
por: Badar, Talha, et al.
Publicado: (2023)

Biallelic disruption of DDX41 activity is associated with distinct genomic and immunophenotypic hallmarks in acute leukemia
por: Tierens, Anne, et al.
Publicado: (2023)

MEF2A suppresses stress responses that trigger DDX41-dependent IFN production
por: Smith, Julian R., et al.
Publicado: (2023)

Las rebeliones campesinas en México, 1819-1906
por: Reina, Leticia
Publicado: (1998)

Las rebeliones campesinas en México, 1819-1906 /
por: Reina, Leticia
Publicado: (1980)

Lunatics and lunatic asylums in early Singapore (1819-1869).
por: Lee, Y K
Publicado: (1973)

Louis Jurine, chirurgien et naturaliste (1751–1819)
por: Spary, E C
Publicado: (2002)

James Watt (1736-1819): culture, innovation and enlightenment
por: Archer-Parré, Caroline, et al.
Publicado: (2020)

A novel bi-alleleic DDX41 mutations in B-cell lymphoblastic leukemia: case report
por: Shin, Woo Yong, et al.
Publicado: (2022)

Clinical features of DDX41 mutation-related diseases: a systematic review with individual patient data
por: Wan, Ziqi, et al.
Publicado: (2021)

R-loop proximity proteomics identifies a role of DDX41 in transcription-associated genomic instability
por: Mosler, Thorsten, et al.
Publicado: (2021)

Next‐generation sequencing reveals the presence of DDX41 mutations in acute lymphoblastic leukemia and aplastic anemia
por: Zhang, Yang, et al.
Publicado: (2021)

DDX41 coordinates RNA splicing and transcriptional elongation to prevent DNA replication stress in hematopoietic cells
por: Shinriki, Satoru, et al.
Publicado: (2022)

Impairment of social behaviors in Arhgef10 knockout mice
por: Lu, Dai-Hua, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_tc5pats30q7ip5ogg9725bgiv4