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W Kern

Showing results (141-150 of 349) with videos related to

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Leukemia|September 14, 2007
A new case with rare e6a2 BCR-ABL fusion transcript developing two new resistance mutations during imatinib mesylate, which were replaced by T315I after subsequent dasatinib treatmentS Schnittger, U Bacher, W Kern, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1989
Influences of corticotropin-releasing hormone, adrenocorticotropin, and cortisol on sleep in normal manJ Born, E Späth-Schwalbe, H Schwakenhofer, et al.
Cancer Genetics and Cytogenetics|June 16, 2001
Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemiaC Schoch, S Bursch, W Kern, et al.
Diabetes Care|August 11, 2000
Adaptation of cognitive function to hypoglycemia in healthy menB Fruehwald-Schultes, J Born, W Kern, et al.
Leukemia|October 30, 2009
Similar patterns of chromosome abnormalities in CML occur in addition to the Philadelphia chromosome with or without tyrosine kinase inhibitor treatmentC Haferlach, U Bacher, S Schnittger, et al.
Leukemia|December 5, 2012
STAT3 mutations are highly specific for large granular lymphocytic leukemiaA Fasan, W Kern, V Grossmann, et al.
Leukemia|June 11, 2016
Subtype-specific patterns of molecular mutations in acute myeloid leukemiaD Rose, T Haferlach, S Schnittger, et al.
Leukemia|September 30, 2016
The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: an analysis of 3307 casesA Stengel, W Kern, T Haferlach, et al.
Biological Psychiatry|March 15, 1991
Sleep disruption alters nocturnal ACTH and cortisol secretory patternsE Späth-Schwalbe, M Gofferje, W Kern, et al.
Leukemia|September 5, 2012
A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98-NSD1 fusion geneA Fasan, C Haferlach, T Alpermann, et al.
Pageof 35

Showing results (141-150 of 349) with videos related to

Sort By:
Pageof 35
Leukemia|September 14, 2007
A new case with rare e6a2 BCR-ABL fusion transcript developing two new resistance mutations during imatinib mesylate, which were replaced by T315I after subsequent dasatinib treatmentS Schnittger, U Bacher, W Kern, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1989
Influences of corticotropin-releasing hormone, adrenocorticotropin, and cortisol on sleep in normal manJ Born, E Späth-Schwalbe, H Schwakenhofer, et al.
Cancer Genetics and Cytogenetics|June 16, 2001
Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemiaC Schoch, S Bursch, W Kern, et al.
Diabetes Care|August 11, 2000
Adaptation of cognitive function to hypoglycemia in healthy menB Fruehwald-Schultes, J Born, W Kern, et al.
Leukemia|October 30, 2009
Similar patterns of chromosome abnormalities in CML occur in addition to the Philadelphia chromosome with or without tyrosine kinase inhibitor treatmentC Haferlach, U Bacher, S Schnittger, et al.
Leukemia|December 5, 2012
STAT3 mutations are highly specific for large granular lymphocytic leukemiaA Fasan, W Kern, V Grossmann, et al.
Leukemia|June 11, 2016
Subtype-specific patterns of molecular mutations in acute myeloid leukemiaD Rose, T Haferlach, S Schnittger, et al.
Leukemia|September 30, 2016
The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: an analysis of 3307 casesA Stengel, W Kern, T Haferlach, et al.
Biological Psychiatry|March 15, 1991
Sleep disruption alters nocturnal ACTH and cortisol secretory patternsE Späth-Schwalbe, M Gofferje, W Kern, et al.
Leukemia|September 5, 2012
A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98-NSD1 fusion geneA Fasan, C Haferlach, T Alpermann, et al.
Pageof 35