Lista de obras - Sabine Strehl - Dominio Público Uruguay

A Mouse Model to Assess STAT3 and STAT5A/B Combined Inhibition in Health and Disease Conditions

scientific article published on 22 August 2019

A highly specific and sensitive fluorescence in situ hybridization assay for the detection of t(4;11)(q21;q23) and concurrent submicroscopic deletions in acute leukaemias

artículo científico publicado en 2002

Acute myelocytic leukemia with t(11;17)(q23;q12-q21) involves a fusion of MLL and AF17

scientific article published on 01 February 2005

All-trans retinoic acid and arsenic trioxide resistance of acute promyelocytic leukemia with the variant STAT5B-RARA fusion gene

article

An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome

artículo científico publicado en 2013

Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome.

artículo científico publicado en 2008

Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL.

artículo científico publicado en 2001

Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14

artículo científico publicado en 1998

Complexity of NOTCH1 juxtamembrane insertion mutations in T-cell acute lymphoblastic leukemia

artículo científico publicado en 2015

Cytogenetic aspects of pediatric germ cell tumors

artículo científico publicado en 1995

Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia

artículo científico publicado en 2007

Diagnostic value of the molecular genetic detection of the t(11;22) translocation in Ewing's tumours

artículo científico publicado en 1994

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group

artículo científico publicado en 2009

ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations

artículo científico publicado en 2008

Ewing's tumor X mouse hybrids expressing the MIC2 antigen: analyses using fluorescence CDD-banding and non-isotopic ISH.

artículo científico publicado en 1992

Expression of PAX5 splice variants: a phenomenon of stress-induced, illegitimate splicing?

scientific article published on 11 April 2011

Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes

artículo científico publicado en 2009

Fluorescence in situ hybridization combined with immunohistochemistry for highly sensitive detection of chromosome 1 aberrations in neuroblastoma

artículo científico publicado en 1993

Functional heterogeneity of PAX5 chimeras reveals insight for leukemia development.

artículo científico publicado en 2014

High-Resolution Analysis of DNA Replication Domain Organization across an R/G-Band Boundary ⬇️

artículo científico publicado el 1 de octubre de 1997

Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukaemia

artículo científico publicado en 2007

Imatinib-induced long-term remission in a relapsed RCSD1-ABL1-positive acute lymphoblastic leukemia

artículo científico publicado en 2016

Incidence and diversity of PAX5 fusion genes in childhood acute lymphoblastic leukemia

artículo científico publicado en 2008

Incidence and outcome of TCF3-PBX1-positive acute lymphoblastic leukemia in Austrian children

artículo científico publicado en 2007

Interphase cytogenetic study of childhood acute lymphoblastic leukemia

artículo científico publicado en 1994

Intragenic amplification of : a novel subgroup in B-cell precursor acute lymphoblastic leukemia?

scientific article published on 14 August 2017

Isochromosome 12p and maternal loss of 1p36 in a pediatric testicular germ cell tumor

article

MEF2C-dysregulated pediatric T-cell acute lymphoblastic leukemia is associated with CDKN1B deletions and a poor response to glucocorticoid therapy

artículo científico publicado en 2017

MIC2 is a specific marker for ewing's sarcoma and peripheral primitive neuroectodermal tumors. Evidence for a common histogenesis of ewing's sarcoma and peripheral primitive neuroectodermal tumors from MIC2 expression and specific chromosome aberrati

article

Mixed lineage leukemia-rearranged childhood pro-B and CD10-negative pre-B acute lymphoblastic leukemia constitute a distinct clinical entity

artículo científico publicado en 2006

Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement.

artículo científico publicado en 2014

Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants

article

Molecular role of the PAX5-ETV6 oncoprotein in promoting B-cell acute lymphoblastic leukemia

artículo científico publicado en 2017

Molecular-cytogenetic characterization of the Vicia faba genome--heterochromatin differentiation, replication patterns and sequence localization

artículo científico publicado en 1998

Multiplex reverse transcriptase-polymerase chain reaction screening in childhood acute myeloblastic leukemia

artículo científico publicado en 2001

Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21

artículo científico publicado en 2003

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

artículo científico publicado en 2008

NQO1 C609T polymorphism in distinct entities of pediatric hematologic neoplasms.

artículo científico publicado en 2004

NUP98 is fused to topoisomerase (DNA) IIbeta 180 kDa (TOP2B) in a patient with acute myeloid leukemia with a new t(3;11)(p24;p15).

artículo científico publicado en 2005

Neuroblastoma cells can actively eliminate supernumerary MYCN gene copies by micronucleus formation--sign of tumour cell revertance?

artículo científico publicado en 1997

New insights to the MLL recombinome of acute leukemias

artículo científico publicado en 2009

Non-random integration of Epstein-Barr virus in lymphoblastoid cell lines.

artículo científico publicado en 1993

Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia: results of an international retrospective study.

artículo científico publicado en 2009

PAX5 fusion genes in t(7;9)(q11.2;p13) leukemia: a case report and review of the literature

artículo científico publicado en 2014

PAX5-AUTS2: a recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia.

artículo científico

PAX5-KIAA1549L: a novel fusion gene in a case of pediatric B-cell precursor acute lymphoblastic leukemia

artículo científico publicado en 2015

PHF6 mutations in T-cell acute lymphoblastic leukemia

artículo científico publicado en 2010

Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors

artículo científico publicado en 1999

Prognostic relevance of TLX3 (HOX11L2) expression in childhood T-cell acute lymphoblastic leukaemia treated with Berlin-Frankfurt-Münster (BFM) protocols containing early and late re-intensification elements

artículo científico publicado en 2009

Prognostic relevance of dic(9;20)(p11;q13) in childhood B-cell precursor acute lymphoblastic leukaemia treated with Berlin-Frankfurt-Münster (BFM) protocols containing an intensive induction and post-induction consolidation therapy

artículo científico publicado en 2010

Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/MLL-rearranged AML patients: results of an international study

artículo científico publicado en 2011

RT-PCR and FISH analysis of acute myeloid leukemia with t(8;16)(p11;p13) and chimeric MOZ and CBP transcripts: breakpoint cluster region and clinical implications

artículo científico publicado en 2004

Regression and progression in neuroblastoma. Does genetics predict tumour behaviour?

artículo científico publicado en 1995

Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization.

artículo científico publicado en 2005

Screening for neuroblastoma

artículo científico publicado en 1994

Searching for prognostic markers in childhood T-cell acute lymphoblastic leukemia

artículo científico publicado en 2006

Spliced MLL fusions: a novel mechanism to generate functional chimeric MLL-MLLT1 transcripts in t(11;19)(q23;p13.3) leukemia.

artículo científico publicado en 2007

Structure of the human TNF receptor 1 (p60) gene (TNFR1) and localization to chromosome 12p13 [corrected]

artículo científico publicado en 1992

The MLL recombinome of acute leukemias

scientific article published on 01 May 2006

The MLL recombinome of acute leukemias in 2013.

artículo científico publicado en 2013

The MLL recombinome of acute leukemias in 2017.

artículo científico

The human LASP1 gene is fused to MLL in an acute myeloid leukemia with t(11;17)(q23;q21).

artículo científico publicado en 2003

The proto-oncogene ERG in megakaryoblastic leukemias

artículo científico publicado en 2005

The role of the Janus-faced transcription factor PAX5-JAK2 in acute lymphoblastic leukemia

artículo científico publicado en 2014

Translocation (12;13) in a case of infantile fibrosarcoma

article

Treatment outcome of CRLF2-rearranged childhood acute lymphoblastic leukaemia: a comparative analysis of the AIEOP-BFM and UK NCRI-CCLG study groups

artículo científico publicado en 2012

Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL

artículo científico publicado en 2019

Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data.

artículo científico publicado en 1994

Lista de obras de Sabine Strehl

A Mouse Model to Assess STAT3 and STAT5A/B Combined Inhibition in Health and Disease Conditions

A highly specific and sensitive fluorescence in situ hybridization assay for the detection of t(4;11)(q21;q23) and concurrent submicroscopic deletions in acute leukaemias

Acute myelocytic leukemia with t(11;17)(q23;q12-q21) involves a fusion of MLL and AF17

All-trans retinoic acid and arsenic trioxide resistance of acute promyelocytic leukemia with the variant STAT5B-RARA fusion gene

An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome

Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome.

Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL.

Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14

Complexity of NOTCH1 juxtamembrane insertion mutations in T-cell acute lymphoblastic leukemia

Cytogenetic aspects of pediatric germ cell tumors

Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia

Diagnostic value of the molecular genetic detection of the t(11;22) translocation in Ewing's tumours

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group

ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations

Ewing's tumor X mouse hybrids expressing the MIC2 antigen: analyses using fluorescence CDD-banding and non-isotopic ISH.

Expression of PAX5 splice variants: a phenomenon of stress-induced, illegitimate splicing?

Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes

Fluorescence in situ hybridization combined with immunohistochemistry for highly sensitive detection of chromosome 1 aberrations in neuroblastoma

Functional heterogeneity of PAX5 chimeras reveals insight for leukemia development.

High-Resolution Analysis of DNA Replication Domain Organization across an R/G-Band Boundary ⬇️

Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukaemia

Imatinib-induced long-term remission in a relapsed RCSD1-ABL1-positive acute lymphoblastic leukemia

Incidence and diversity of PAX5 fusion genes in childhood acute lymphoblastic leukemia

Incidence and outcome of TCF3-PBX1-positive acute lymphoblastic leukemia in Austrian children

Interphase cytogenetic study of childhood acute lymphoblastic leukemia

Intragenic amplification of : a novel subgroup in B-cell precursor acute lymphoblastic leukemia?

Isochromosome 12p and maternal loss of 1p36 in a pediatric testicular germ cell tumor

MEF2C-dysregulated pediatric T-cell acute lymphoblastic leukemia is associated with CDKN1B deletions and a poor response to glucocorticoid therapy

MIC2 is a specific marker for ewing's sarcoma and peripheral primitive neuroectodermal tumors. Evidence for a common histogenesis of ewing's sarcoma and peripheral primitive neuroectodermal tumors from MIC2 expression and specific chromosome aberrati

Mixed lineage leukemia-rearranged childhood pro-B and CD10-negative pre-B acute lymphoblastic leukemia constitute a distinct clinical entity

Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement.

Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants

Molecular role of the PAX5-ETV6 oncoprotein in promoting B-cell acute lymphoblastic leukemia

Molecular-cytogenetic characterization of the Vicia faba genome--heterochromatin differentiation, replication patterns and sequence localization

Multiplex reverse transcriptase-polymerase chain reaction screening in childhood acute myeloblastic leukemia

Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

NQO1 C609T polymorphism in distinct entities of pediatric hematologic neoplasms.

NUP98 is fused to topoisomerase (DNA) IIbeta 180 kDa (TOP2B) in a patient with acute myeloid leukemia with a new t(3;11)(p24;p15).

Neuroblastoma cells can actively eliminate supernumerary MYCN gene copies by micronucleus formation--sign of tumour cell revertance?

New insights to the MLL recombinome of acute leukemias

Non-random integration of Epstein-Barr virus in lymphoblastoid cell lines.

Novel prognostic subgroups in childhood 11q23/MLL-rearranged acute myeloid leukemia: results of an international retrospective study.

PAX5 fusion genes in t(7;9)(q11.2;p13) leukemia: a case report and review of the literature

PAX5-AUTS2: a recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia.

PAX5-KIAA1549L: a novel fusion gene in a case of pediatric B-cell precursor acute lymphoblastic leukemia

PHF6 mutations in T-cell acute lymphoblastic leukemia

Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors

Prognostic relevance of TLX3 (HOX11L2) expression in childhood T-cell acute lymphoblastic leukaemia treated with Berlin-Frankfurt-Münster (BFM) protocols containing early and late re-intensification elements

Prognostic relevance of dic(9;20)(p11;q13) in childhood B-cell precursor acute lymphoblastic leukaemia treated with Berlin-Frankfurt-Münster (BFM) protocols containing an intensive induction and post-induction consolidation therapy

Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/MLL-rearranged AML patients: results of an international study

RT-PCR and FISH analysis of acute myeloid leukemia with t(8;16)(p11;p13) and chimeric MOZ and CBP transcripts: breakpoint cluster region and clinical implications

Regression and progression in neuroblastoma. Does genetics predict tumour behaviour?

Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization.

Screening for neuroblastoma

Searching for prognostic markers in childhood T-cell acute lymphoblastic leukemia

Spliced MLL fusions: a novel mechanism to generate functional chimeric MLL-MLLT1 transcripts in t(11;19)(q23;p13.3) leukemia.

Structure of the human TNF receptor 1 (p60) gene (TNFR1) and localization to chromosome 12p13 [corrected]

The MLL recombinome of acute leukemias

The MLL recombinome of acute leukemias in 2013.

The MLL recombinome of acute leukemias in 2017.

The human LASP1 gene is fused to MLL in an acute myeloid leukemia with t(11;17)(q23;q21).

The proto-oncogene ERG in megakaryoblastic leukemias

The role of the Janus-faced transcription factor PAX5-JAK2 in acute lymphoblastic leukemia

Translocation (12;13) in a case of infantile fibrosarcoma

Treatment outcome of CRLF2-rearranged childhood acute lymphoblastic leukaemia: a comparative analysis of the AIEOP-BFM and UK NCRI-CCLG study groups

Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL

Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data.