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Simone Feurstein

Showing results (11-20 of 22) with videos related to

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Genes, Chromosomes & Cancer|July 1, 2010
Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGHInka Praulich, Marcel Tauscher, Gudrun Göhring, et al.
BMC Genomics|September 13, 2014
Haploinsufficiency of ETV6 and CDKN1B in patients with acute myeloid leukemia and complex karyotypeSimone Feurstein, Frank G Rücker, Lars Bullinger, et al.
Blood Advances|October 27, 2020
Heterozygous germ line CSF3R variants as risk alleles for development of hematologic malignanciesAmy M Trottier, Lawrence J Druhan, Ira L Kraft, et al.
Ejhaem|December 5, 2022
Concurrent light chain amyloidosis and proximal tubulopathy: Insights into different aggregation behavior-A case reportSimone Feurstein, Julian Zoller, Constantin Schwab, et al.
Human Mutation|August 13, 2021
GATA2 deficiency syndrome: A decade of discoveryClaire C Homan, Parvathy Venugopal, Peer Arts, et al.
Leukemia|October 20, 2022
Significance of hereditary gene alterations for the pathogenesis of adult bone marrow failure versus myeloid neoplasiaYasuo Kubota, Misam Zawit, Jibran Durrani, et al.
Blood Advances|January 25, 2018
Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignanciesMichael W Drazer, Sabah Kadri, Madina Sukhanova, et al.
Blood|August 15, 2022
Germ line predisposition variants occur in myelodysplastic syndrome patients of all agesSimone Feurstein, Amy M Trottier, Noel Estrada-Merly, et al.
Blood Advances|October 9, 2020
Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentationsSimone Feurstein, Ayodeji Adegunsoye, Danijela Mojsilovic, et al.
Leukemia|April 14, 2021
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancerDeepak Singhal, Christopher N Hahn, Simone Feurstein, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Genes, Chromosomes & Cancer|July 1, 2010
Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGHInka Praulich, Marcel Tauscher, Gudrun Göhring, et al.
BMC Genomics|September 13, 2014
Haploinsufficiency of ETV6 and CDKN1B in patients with acute myeloid leukemia and complex karyotypeSimone Feurstein, Frank G Rücker, Lars Bullinger, et al.
Blood Advances|October 27, 2020
Heterozygous germ line CSF3R variants as risk alleles for development of hematologic malignanciesAmy M Trottier, Lawrence J Druhan, Ira L Kraft, et al.
Ejhaem|December 5, 2022
Concurrent light chain amyloidosis and proximal tubulopathy: Insights into different aggregation behavior-A case reportSimone Feurstein, Julian Zoller, Constantin Schwab, et al.
Human Mutation|August 13, 2021
GATA2 deficiency syndrome: A decade of discoveryClaire C Homan, Parvathy Venugopal, Peer Arts, et al.
Leukemia|October 20, 2022
Significance of hereditary gene alterations for the pathogenesis of adult bone marrow failure versus myeloid neoplasiaYasuo Kubota, Misam Zawit, Jibran Durrani, et al.
Blood Advances|January 25, 2018
Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignanciesMichael W Drazer, Sabah Kadri, Madina Sukhanova, et al.
Blood|August 15, 2022
Germ line predisposition variants occur in myelodysplastic syndrome patients of all agesSimone Feurstein, Amy M Trottier, Noel Estrada-Merly, et al.
Blood Advances|October 9, 2020
Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentationsSimone Feurstein, Ayodeji Adegunsoye, Danijela Mojsilovic, et al.
Leukemia|April 14, 2021
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancerDeepak Singhal, Christopher N Hahn, Simone Feurstein, et al.
Pageof 3