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Stem Cell Research
|
April 22, 2016
GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemia
Georgi Manukjan, Tim Ripperger, Letizia Venturini, et al.
Human Molecular Genetics
|
December 14, 2006
Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome
Christian P Kratz, Doris Steinemann, Charlotte M Niemeyer, et al.
Experimental Hematology
|
June 15, 2015
Expression of the ETS transcription factor GABPα is positively correlated to the BCR-ABL1/ABL1 ratio in CML patients and affects imatinib sensitivity in vitro
Georgi Manukjan, Tim Ripperger, Laura Santer, et al.
European Journal of Medical Genetics
|
September 7, 2016
NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?
Caroline Scholz, Doris Steinemann, Madeleine Mälzer, et al.
Stem Cell Research
|
December 15, 2019
Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual
Nina V Fuchs, Maximilian Schieck, Michaela Neuenkirch, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2018
KBG syndrome patient due to 16q24.3 microdeletion presenting with a paratesticular rhabdoid tumor: Coincidence or cancer predisposition?
Astrid Behnert, Bernd Auber, Doris Steinemann, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
June 16, 2009
Bronchial epithelial cells as a new source for differential transcriptome analysis after lung transplantation
Britta Skawran, Martin Dierich, Doris Steinemann, et al.
Cancer Genetics and Cytogenetics
|
May 19, 2005
BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinib
Dorothea Gadzicki, Nils von Neuhoff, Doris Steinemann, et al.
Oncogene
|
March 28, 2003
Frequent epigenetic inactivation of the RASSF1A gene in hepatocellular carcinoma
Undraga Schagdarsurengin, Ludwig Wilkens, Doris Steinemann, et al.
European Journal of Medical Genetics
|
March 5, 2018
12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature
Frederik Heldt, Hannah Wallaschek, Tim Ripperger, et al.
Page
of 16
Search research articles
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Showing results (21-30 of 158) with videos related to
Sort By:
Page
of 16
Stem Cell Research
|
April 22, 2016
GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemia
Georgi Manukjan, Tim Ripperger, Letizia Venturini, et al.
Human Molecular Genetics
|
December 14, 2006
Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome
Christian P Kratz, Doris Steinemann, Charlotte M Niemeyer, et al.
Experimental Hematology
|
June 15, 2015
Expression of the ETS transcription factor GABPα is positively correlated to the BCR-ABL1/ABL1 ratio in CML patients and affects imatinib sensitivity in vitro
Georgi Manukjan, Tim Ripperger, Laura Santer, et al.
European Journal of Medical Genetics
|
September 7, 2016
NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?
Caroline Scholz, Doris Steinemann, Madeleine Mälzer, et al.
Stem Cell Research
|
December 15, 2019
Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual
Nina V Fuchs, Maximilian Schieck, Michaela Neuenkirch, et al.
American Journal of Medical Genetics. Part A
|
April 27, 2018
KBG syndrome patient due to 16q24.3 microdeletion presenting with a paratesticular rhabdoid tumor: Coincidence or cancer predisposition?
Astrid Behnert, Bernd Auber, Doris Steinemann, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery
|
June 16, 2009
Bronchial epithelial cells as a new source for differential transcriptome analysis after lung transplantation
Britta Skawran, Martin Dierich, Doris Steinemann, et al.
Cancer Genetics and Cytogenetics
|
May 19, 2005
BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinib
Dorothea Gadzicki, Nils von Neuhoff, Doris Steinemann, et al.
Oncogene
|
March 28, 2003
Frequent epigenetic inactivation of the RASSF1A gene in hepatocellular carcinoma
Undraga Schagdarsurengin, Ludwig Wilkens, Doris Steinemann, et al.
European Journal of Medical Genetics
|
March 5, 2018
12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature
Frederik Heldt, Hannah Wallaschek, Tim Ripperger, et al.
Page
of 16