Found: 59
Select item for more details and to access through your institution.
Re: B-cell non-Hodgkin's lymphoma: evidence for the t(14;18) translocation in all hematopoietic cell lineages.
- Published in:
- 1997
- By:
- Publication type:
- commentary
Human BRCA1-Associated Breast Cancer: No Increase in Numerical Chromosomal Instability Compared to Sporadic Tumors.
- Published in:
- Cytogenetic & Genome Research, 2011, v. 135, n. 2, p. 84, doi. 10.1159/000332005
- By:
- Publication type:
- Article
Cytogenetic characteristics of a murine in vitro model for the human anaplastic large cell lymphoma (ALCL).
- Published in:
- Cytogenetic & Genome Research, 2006, v. 114, n. 3/4, p. 292, doi. 10.1159/000094216
- By:
- Publication type:
- Article
Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progession-related mechanisms.
- Published in:
- Cytogenetic & Genome Research, 2006, v. 112, n. 3/4, p. 213, doi. 10.1159/000089873
- By:
- Publication type:
- Article
Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.
- Published in:
- Oncogene, 2007, v. 26, n. 39, p. 5816, doi. 10.1038/sj.onc.1210361
- By:
- Publication type:
- Article
Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Diagnosis of monogenic liver diseases in childhood by next‐generation sequencing.
- Published in:
- Clinical Genetics, 2018, v. 93, n. 3, p. 665, doi. 10.1111/cge.13120
- By:
- Publication type:
- Article
The proline TP53 variant stimulates likely lymphangiogenesis in an orthotopic mouse model of pancreatic cancer.
- Published in:
- British Journal of Cancer, 2012, v. 106, n. 2, p. 348, doi. 10.1038/bjc.2011.521
- By:
- Publication type:
- Article
Preserved reticulin network in a case of hepatocellular carcinoma.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Erratum zu: Massive parallele Sequenzierung in der Diagnostik hereditärer BRCA1/2-Mutationen.
- Published in:
- 2014
- By:
- Publication type:
- Erratum
Massive parallele Sequenzierung in der Diagnostik hereditärer BRCA1-/-2-Mutationen.
- Published in:
- Medizinische Genetik, 2014, v. 26, n. 2, p. 255, doi. 10.1007/s11825-014-0443-y
- By:
- Publication type:
- Article
Mosaiktrisomie 8p11.21q11.21 als Prädisposition für myeloische Leukämien.
- Published in:
- Medizinische Genetik, 2012, v. 24, n. 1, p. 33, doi. 10.1007/s11825-012-0316-1
- By:
- Publication type:
- Article
Erblicher Brust- und Eierstockkrebs.
- Published in:
- Medizinische Genetik, 2007, v. 19, n. 2, p. 202, doi. 10.1007/s11825-007-0019-1
- By:
- Publication type:
- Article
Genetische Prädisposition für Krebserkrankungen im Kindesalter.
- Published in:
- Der Pathologe, 2018, v. 39, p. 306, doi. 10.1007/s00292-018-0542-7
- By:
- Publication type:
- Article
Low frequency of calreticulin mutations in MDS patients.
- Published in:
- Leukemia (08876924), 2014, v. 28, n. 9, p. 1933, doi. 10.1038/leu.2014.165
- By:
- Publication type:
- Article
Activation of Evi1 inhibits cell cycle progression and differentiation of hematopoietic progenitor cells.
- Published in:
- Leukemia (08876924), 2013, v. 27, n. 5, p. 1127, doi. 10.1038/leu.2012.355
- By:
- Publication type:
- Article
Analysis of NUP98/NSD1 translocations in adult AML and MDS patients.
- Published in:
- Leukemia (08876924), 2013, v. 27, n. 3, p. 750, doi. 10.1038/leu.2012.249
- By:
- Publication type:
- Article
Altered miRNA and gene expression in acute myeloid leukemia with complex karyotype identify networks of prognostic relevance.
- Published in:
- Leukemia (08876924), 2013, v. 27, n. 2, p. 353, doi. 10.1038/leu.2012.208
- By:
- Publication type:
- Article
Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential.
- Published in:
- Leukemia (08876924), 2012, v. 26, n. 10, p. 2302, doi. 10.1038/leu.2012.132
- By:
- Publication type:
- Article
SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications.
- Published in:
- Leukemia (08876924), 2012, v. 26, n. 5, p. 1137, doi. 10.1038/leu.2011.321
- By:
- Publication type:
- Article
Prognostic implications and molecular associations of NADH dehydrogenase subunit 4 (ND4) mutations in acute myeloid leukemia.
- Published in:
- Leukemia (08876924), 2012, v. 26, n. 2, p. 289, doi. 10.1038/leu.2011.200
- By:
- Publication type:
- Article
Telomere shortening, clonal evolution and disease progression in myelodysplastic syndrome patients with 5q deletion treated with lenalidomide.
- Published in:
- 2012
- By:
- Publication type:
- Letter
Stable and reproducible engraftment of primary adult and pediatric acute myeloid leukemia in NSG mice.
- Published in:
- 2011
- By:
- Publication type:
- Letter
ICSBP promoter methylation in myelodysplastic syndromes and acute myeloid leukaemia.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Identification of disease- and therapy-associated proteome changes in the sera of patients with myelodysplastic syndromes and del(5q).
- Published in:
- Leukemia (08876924), 2010, v. 24, n. 11, p. 1875, doi. 10.1038/leu.2010.182
- By:
- Publication type:
- Article
A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?
- Published in:
- 2009
- By:
- Publication type:
- Letter
Global increase in DNA methylation in patients with myelodysplastic syndrome.
- Published in:
- Leukemia (08876924), 2008, v. 22, n. 10, p. 1954, doi. 10.1038/leu.2008.76
- By:
- Publication type:
- Article
Leukemia induction after a single retroviral vector insertion in Evi1 or Prdm16.
- Published in:
- Leukemia (08876924), 2008, v. 22, n. 8, p. 1519, doi. 10.1038/leu.2008.118
- By:
- Publication type:
- Article
Marrow fibrosis predicts early fatal marrow failure in patients with myelodysplastic syndromes.
- Published in:
- Leukemia (08876924), 2008, v. 22, n. 2, p. 313, doi. 10.1038/sj.leu.2405030
- By:
- Publication type:
- Article
Marrow fibrosis and its relevance during imatinib treatment of chronic myeloid leukemia.
- Published in:
- Leukemia (08876924), 2007, v. 21, n. 12, p. 2420, doi. 10.1038/sj.leu.2404917
- By:
- Publication type:
- Article
Remarkable leukemogenic potency and quality of a constitutively active neurotrophin receptor, ΔTrkA.
- Published in:
- Leukemia (08876924), 2007, v. 21, n. 10, p. 2171, doi. 10.1038/sj.leu.2404882
- By:
- Publication type:
- Article
Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Chromosomal aberrations in congenital bone marrow failure disorders—an early indicator for leukemogenesis?
- Published in:
- Annals of Hematology, 2007, v. 86, n. 10, p. 733, doi. 10.1007/s00277-007-0337-z
- By:
- Publication type:
- Article
Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Cytogenetic subtyping of diffuse large B-cell lymphomas.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Assignment<FOOTREF>[sup 1] </FOOTREF> of the human FAN protein gene (NSMAF) to human chromosome region 8q12→q13 by in situ hybridization.
- Published in:
- Cytogenetics & Cell Genetics, 1999, v. 87, n. 1/2, p. 115, doi. 10.1159/000015375
- By:
- Publication type:
- Article
Assignment<FOOTREF>[sup 1] </FOOTREF> of human proliferation associated p100 gene (C20orf1) to human chromosome band 20q11.2 by in situ hybridization.
- Published in:
- Cytogenetics & Cell Genetics, 1999, v. 84, n. 3/4, p. 182, doi. 10.1159/000015251
- By:
- Publication type:
- Article
Assignment<FOOTREF>[sup 1] </FOOTREF> of human putative tumor suppressor genes ST13 (alias SNC6) and ST14 (alias SNC19) to human chromosome bands 22q13 and 11q24→q25 by in situ hybridization.
- Published in:
- Cytogenetics & Cell Genetics, 1998, v. 83, n. 1/2, p. 56, doi. 10.1159/000015125
- By:
- Publication type:
- Article
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 3, p. 120, doi. 10.1159/000341935
- By:
- Publication type:
- Article
THE ROLE OF THE SPLEEN AFTER BONE MARROW TRANSPLANTATION FOR PRIMARY MYELOFIBROSIS.
- Published in:
- British Journal of Haematology, 1992, v. 81, n. 4, p. 616, doi. 10.1111/j.1365-2141.1992.tb03004.x
- By:
- Publication type:
- Article
Lymphohaematopoietic chimaerism after bone marrow transplantation for chronic myeloid leukaemia: results of simultaneous cytogenetic analyses on T-cell colonies, myeloid, and erythroid progenitor cells.
- Published in:
- British Journal of Haematology, 1991, v. 78, n. 3, p. 334, doi. 10.1111/j.1365-2141.1991.tb04446.x
- By:
- Publication type:
- Article
TEGDMA Causes Apoptosis in Primary Human Gingival Fibroblasts.
- Published in:
- Journal of Dental Research, 2003, v. 82, n. 10, p. 814, doi. 10.1177/154405910308201010
- By:
- Publication type:
- Article
Functional characterization of a JAG1 promoter variant in a patient with clinically observed Alagille Syndrome.
- Published in:
- Journal of Pediatric Gastroenterology & Nutrition, 2022, v. 74, p. 704, doi. 10.1097/MPG.0000000000003446
- By:
- Publication type:
- Article
Functional characterization of variants of unknown significance in the Wilson disease-associated ATP7B gene.
- Published in:
- Journal of Pediatric Gastroenterology & Nutrition, 2022, v. 74, p. 679, doi. 10.1097/MPG.0000000000003446
- By:
- Publication type:
- Article
Hyperactivation of mTORC1 and mTORC2 by multiple oncogenic events causes addiction to eIF4E-dependent mRNA translation in T-cell leukemia.
- Published in:
- Oncogene, 2015, v. 34, n. 27, p. 3593, doi. 10.1038/onc.2014.290
- By:
- Publication type:
- Article
Selection for Evi1 activation in myelomonocytic leukemia induced by hyperactive signaling through wild-type NRas.
- Published in:
- Oncogene, 2013, v. 32, n. 25, p. 3028, doi. 10.1038/onc.2012.329
- By:
- Publication type:
- Article
Loss of heterozygosity on chromosome 6q14–q24 is associated with poor outcome in children and adolescents with T-cell lymphoblastic lymphoma.
- Published in:
- Leukemia (08876924), 2006, v. 20, n. 8, p. 1422, doi. 10.1038/sj.leu.2404275
- By:
- Publication type:
- Article
Consensus guidelines for microarray gene expression analyses in leukemia from three European leukemia networks.
- Published in:
- Leukemia (08876924), 2006, v. 20, n. 8, p. 1385, doi. 10.1038/sj.leu.2404274
- By:
- Publication type:
- Article
Unsupervised proteome analysis of human leukaemia cells identifies the Valosin-containing protein as a putative marker for glucocorticoid resistance.
- Published in:
- Leukemia (08876924), 2006, v. 20, n. 5, p. 820, doi. 10.1038/sj.leu.2404162
- By:
- Publication type:
- Article
Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential.
- Published in:
- 2006
- By:
- Publication type:
- journal article