Martin Erdel


Ontology type: schema:Person     


Person Info

NAME

Martin

SURNAME

Erdel

Publications in SciGraph latest 50 shown

  • 2018-12 Overexpression of the proneural transcription factor ASCL1 in chronic lymphocytic leukemia with a t(12;14)(q23.2;q32.3) in MOLECULAR CYTOGENETICS
  • 2014-06 Switch of the mutation type of the NPM1 gene in acute myeloid leukemia (AML): relapse or secondary AML? in BLOOD CANCER JOURNAL
  • 2011-12 Characterization of a newly identified ETV6-NTRK3 fusion transcript in acute myeloid leukemia in DIAGNOSTIC PATHOLOGY
  • 2011-09 Regulation of transcription factor E2F3a and its clinical relevance in ovarian cancer in ONCOGENE
  • 2010-03 Successful treatment of MDS with lenalidomide, complicated by transient autoimmune hemolysis in ANNALS OF HEMATOLOGY
  • 2008-07 Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association) in WIENER KLINISCHE WOCHENSCHRIFT
  • 2008-05 Fludarabine/intermediate-dose cytarabine with or without allogeneic hematopoietic stem cell transplantation in poor-risk leukemia: a single center experience in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2008-03 Complete cytogenetic remission in a patient with FIP1L1-PDGFRA fusion negative chronic eosinophilic leukemia associated with atypical thrombotic events in MEMO - MAGAZINE OF EUROPEAN MEDICAL ONCOLOGY
  • 2004-05 Cyclin E dysregulation and chromosomal instability in endometrial cancer in ONCOGENE
  • 2003-04-17 Studies on Androgen Receptor Mutations and Amplification in Human Prostate Cancer in PROSTATE CANCER METHODS AND PROTOCOLS
  • 2002-06 The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2002-03 Molecular genetics and structural genomics of the human protein kinase C gene module in GENOME BIOLOGY
  • 2001-09 High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization in IMMUNOGENETICS
  • 2000-09 Mutation analysis in glycogen storage disease type 1 non-a in HUMAN GENETICS
  • 1999-09 Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system in BRITISH JOURNAL OF CANCER
  • 1999-04 Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH in NATURE GENETICS
  • 1999-01 Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1998-09 Molecular characterization of the human protein kinase C θ* gene locus (PRKCQ) in MOLECULAR GENETICS AND GENOMICS
  • 1998-01 Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1997-04 Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype in HUMAN GENETICS
  • 1996-06 Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10) in HUMAN GENETICS
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