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Proceedings of the National Academy of Sciences of the United States of America
|
August 23, 2017
Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci
Randal J Westrick, Kärt Tomberg, Amy E Siebert, et al.
Blood Cancer Journal
|
May 30, 2023
Daratumumab, carfilzomib, and pomalidomide for the treatment of POEMS syndrome: The Mayo Clinic Experience
I Vaxman, S K Kumar, F Buadi, et al.
Leukemia
|
June 17, 2024
Correction: Outcomes among newly diagnosed AL amyloidosis patients with a very high NT-proBNP: implications for trial design
I Vaxman, S K Kumar, F Buadi, et al.
Cancer Discovery
|
May 29, 2014
Vulnerabilities of PTEN-TP53-deficient prostate cancers to compound PARP-PI3K inhibition
Enrique González-Billalabeitia, Nina Seitzer, Su Jung Song, et al.
Leukemia
|
May 22, 2021
Outcomes among newly diagnosed AL amyloidosis patients with a very high NT-proBNP: implications for trial design
I Vaxman, S K Kumar, F Buadi, et al.
Nature Communications
|
April 8, 2016
Large-scale production of megakaryocytes from human pluripotent stem cells by chemically defined forward programming
Thomas Moreau, Amanda L Evans, Louella Vasquez, et al.
Nature Communications
|
July 29, 2017
Corrigendum: Large-scale production of megakaryocytes from human pluripotent stem cells by chemically defined forward programming
Thomas Moreau, Amanda L Evans, Louella Vasquez, et al.
Blood Cancer Journal
|
December 8, 2021
"Real-life" data of the efficacy and safety of belantamab mafodotin in relapsed multiple myeloma-the Mayo Clinic experience
I Vaxman, J Abeykoon, A Dispenzieri, et al.
Elife
|
December 10, 2016
Assessing the mechanism and therapeutic potential of modulators of the human Mediator complex-associated protein kinases
Paul A Clarke, Maria-Jesus Ortiz-Ruiz, Robert TePoele, et al.
Nature Genetics
|
February 28, 2012
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
Cornelis A Albers, Dirk S Paul, Harald Schulze, et al.
Page
of 39
Search research articles
Search
Showing results (371-380 of 381) with videos related to
Sort By:
Page
of 39
Proceedings of the National Academy of Sciences of the United States of America
|
August 23, 2017
Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci
Randal J Westrick, Kärt Tomberg, Amy E Siebert, et al.
Blood Cancer Journal
|
May 30, 2023
Daratumumab, carfilzomib, and pomalidomide for the treatment of POEMS syndrome: The Mayo Clinic Experience
I Vaxman, S K Kumar, F Buadi, et al.
Leukemia
|
June 17, 2024
Correction: Outcomes among newly diagnosed AL amyloidosis patients with a very high NT-proBNP: implications for trial design
I Vaxman, S K Kumar, F Buadi, et al.
Cancer Discovery
|
May 29, 2014
Vulnerabilities of PTEN-TP53-deficient prostate cancers to compound PARP-PI3K inhibition
Enrique González-Billalabeitia, Nina Seitzer, Su Jung Song, et al.
Leukemia
|
May 22, 2021
Outcomes among newly diagnosed AL amyloidosis patients with a very high NT-proBNP: implications for trial design
I Vaxman, S K Kumar, F Buadi, et al.
Nature Communications
|
April 8, 2016
Large-scale production of megakaryocytes from human pluripotent stem cells by chemically defined forward programming
Thomas Moreau, Amanda L Evans, Louella Vasquez, et al.
Nature Communications
|
July 29, 2017
Corrigendum: Large-scale production of megakaryocytes from human pluripotent stem cells by chemically defined forward programming
Thomas Moreau, Amanda L Evans, Louella Vasquez, et al.
Blood Cancer Journal
|
December 8, 2021
"Real-life" data of the efficacy and safety of belantamab mafodotin in relapsed multiple myeloma-the Mayo Clinic experience
I Vaxman, J Abeykoon, A Dispenzieri, et al.
Elife
|
December 10, 2016
Assessing the mechanism and therapeutic potential of modulators of the human Mediator complex-associated protein kinases
Paul A Clarke, Maria-Jesus Ortiz-Ruiz, Robert TePoele, et al.
Nature Genetics
|
February 28, 2012
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
Cornelis A Albers, Dirk S Paul, Harald Schulze, et al.
Page
of 39