J. Schoumans

Discipline

Psychologie (2) Histoire, Philosophie et Sociologie des sciences (2) Sociologie (1) Sciences de l'information et de la communication (1) Anthropologie biologique (1)

Type de document

Articles (15) Recensions (2)

Co-auteur

Date

Source

Mot-clé

Human beings (7) analyse (6) Patients (6) Analysis (6) Patients (6) gène (5) Genes (5) ADN (4) maladie (4) Tumors (4) DNA (4) maladie (4) roman (4) association (3) mutation (3) modèle (3) poisson (3) survie (3) Cytogenetics (3) Treatment (3) Cases (3) Transcription (3) Survival (3) Social groups (3) Medicine (3) Leukemia (3) Fishes (3) Expression (3) Example (3) Cytogenetics (3)

Documents écrit par J. Schoumans (15) | parle de J. Schoumans (0)

Description of an Institutional Cohort of Myeloid Neoplasms Carrying ETV6-Locus Deletions or ETV6 Rearrangements.
V. Papadopoulou et al. (2023)
Venetoclax combined with FLAG-based chemotherapy induces an early and deep response in mixed-phenotype-acute leukemia.
A. Ségot et al. (1 mars 2022)
Isolated skin infiltration by a blastic plasmacytoid dendritic cell neoplasm.
G. Stalder et al.
Daratumumab and venetoclax in combination with chemotherapy provide sustained molecular remission in relapsed/refractory CD19, CD20, and CD22 negative acute B lymphoblastic leukemia with KMT2A-AFF1 transcript.
S. Voruz et al. (20 déc. 2021)
The noradrenergic profile of plasma metanephrine in neuroblastoma patients is reproduced in xenograft mice models and arise from PNMT downregulation.
K. Abid et al. (5 janv. 2021)
Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity: a multi-center study.
A.C. Leeksma et al. (1 janv. 2021)
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasms: reponse to the comments from the Francophone Group of Hematological Cytogenetics (GFCH).
K.A. Rack et al.
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasms
K. A. Rack et al.
MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences.
L'Abbate A. et al.
Laboratory Genetic Testing in Clinical Practice 2016.
O. Cogulu et al. (2017)
t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.
L'Abbate A. et al. (2015)
Laboratory genetic testing in clinical practice 2014.
O. Cogulu et al. (2015)
Evolution of Genetic Techniques: Past, Present, and Beyond.
A.A. Durmaz et al. (2015)
A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination.
E. Enervald et al. (18 nov. 2013)
Mutation screening of patients with Alzheimer disease identifies APP locus duplication in a Swedish patient.
H. Thonberg et al. (2011)