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Gudrun Göhring (1974-)

Name	Gudrun Göhring
Zeit	1974- (Lebensdaten)
Ort	Hannover (Wirkungsort) Deutschland
Akademischer Grad bzw. Titel	Prof. Dr. med.
Variante	Gudrun Michaelsen (Zeitweiser Name)
Beziehung	Medizinische Hochschule Hannover Medizinische Hochschule Hannover. Institut für Humangenetik
Weitere Angaben	Habil. Fach Humangenetik an der Medizinischen Hochschule Hannover (2010)
Datensatztyp	Person
GND-Nummer	12468100X
Datensatz-ID	12468100X
Beteiligt an alle anzeigen A novel classification of hematologic conditions in patients with Fanconi anemia Panel-based RNA fusion sequencing improves diagnostics of pediatric acute myeloid leukemia Die unbalancierte Translokation der(5;17) resultiert in einem Verlust von TP53 als rekurrente Aberration in myelodysplastischen Syndromen und akuter myeloischer Leukämie mit komplexem Karyotyp Role of chromatin localization in respect to acute myeloid leukemia progression Somatic variant profiling in chronic phase pediatric chronic myeloid leukemia Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome Wildtype heterogeneity contributes to clonal variability in genome edited cells P816: Transient monosomy 7 in SAMD9/9L syndromes: is it safe to watch and wait? Wildtype heterogeneity contributes to clonal variability in genome edited cells Germline POT1 deregulation can predispose to myeloid malignancies in childhood Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome Deciphering the oncogenic network of PRC2 loss guided leukemogenesis Establishment and characterization of a sclerosing spindle cell rhabdomyosarcoma cell line with a complex genomic profile Adding dasatinib to intensive treatment in core-binding factor acute myeloid leukemia—results of the AMLSG 11-08 trial Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease Einfluss chromosomaler Instabilität auf die maligne Transformation hämatopoetischer Stammzellen am Beispiel des myelodysplastischen Syndroms Einfluß von MDR1-Modulatoren auf die Chemotherapie kindlicher Lebertumoren in vitro

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Katalog der Deutschen Nationalbibliothek

Gudrun Göhring (1974-)

A novel classification of hematologic conditions in patients with Fanconi anemia

Panel-based RNA fusion sequencing improves diagnostics of pediatric acute myeloid leukemia

Die unbalancierte Translokation der(5;17) resultiert in einem Verlust von TP53 als rekurrente Aberration in myelodysplastischen Syndromen und akuter myeloischer Leukämie mit komplexem Karyotyp

Role of chromatin localization in respect to acute myeloid leukemia progression

Somatic variant profiling in chronic phase pediatric chronic myeloid leukemia

Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome

Wildtype heterogeneity contributes to clonal variability in genome edited cells

P816: Transient monosomy 7 in SAMD9/9L syndromes: is it safe to watch and wait?

Wildtype heterogeneity contributes to clonal variability in genome edited cells

Germline POT1 deregulation can predispose to myeloid malignancies in childhood

Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome

Deciphering the oncogenic network of PRC2 loss guided leukemogenesis

Establishment and characterization of a sclerosing spindle cell rhabdomyosarcoma cell line with a complex genomic profile

Adding dasatinib to intensive treatment in core-binding factor acute myeloid leukemia—results of the AMLSG 11-08 trial

Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN

Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

Einfluss chromosomaler Instabilität auf die maligne Transformation hämatopoetischer Stammzellen am Beispiel des myelodysplastischen Syndroms

Einfluß von MDR1-Modulatoren auf die Chemotherapie kindlicher Lebertumoren in vitro