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Cold Spring Harbor Molecular Case Studies
|
June 22, 2022
Incidental discovery of acute myeloid leukemia during liquid biopsy of a lung cancer patient
Dingani Nkosi, Caroline A Miller, Audrey N Jajosky, et al.
Cold Spring Harbor Molecular Case Studies
|
June 22, 2022
WP1066 induces cell death in a schwannomatosis patient-derived schwannoma cell line
Abdulrahman Allaf, Berta Victoria, Rosa Rosario, et al.
Cold Spring Harbor Molecular Case Studies
|
January 13, 2021
Refractory alveolar rhabdomyosarcoma in an 11-year-old male
Cora A Ricker, Andrew D Woods, William Simonson, et al.
Cold Spring Harbor Molecular Case Studies
|
June 17, 2017
Successful immune checkpoint blockade in a patient with advanced stage microsatellite-unstable biliary tract cancer
Elena Czink, Matthias Kloor, Benjamin Goeppert, et al.
Cold Spring Harbor Molecular Case Studies
|
September 15, 2016
A novel de novo mutation in ATP1A3 and childhood-onset schizophrenia
Niklas Smedemark-Margulies, Catherine A Brownstein, Sigella Vargas, et al.
Cold Spring Harbor Molecular Case Studies
|
September 15, 2016
Testing ERBB2 p.L755S kinase domain mutation as a druggable target in a patient with advanced colorectal cancer
Kyaw L Aung, Tracy L Stockley, Stefano Serra, et al.
Cold Spring Harbor Molecular Case Studies
|
February 12, 2022
Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplication
Esko A Kautto, Kathleen M Schieffer, Sean McGrath, et al.
Cold Spring Harbor Molecular Case Studies
|
January 29, 2022
Inherited and de novo variants extend the etiology of <i>TAOK1</i>-associated neurodevelopmental disorder
Jesse M Hunter, Lauren J Massingham, Kandamurugu Manickam, et al.
Cold Spring Harbor Molecular Case Studies
|
February 15, 2022
Ethylmalonic encephalopathy masquerading as meningococcemia
Ari Horton, Kai Mun Hong, Dinusha Pandithan, et al.
Cold Spring Harbor Molecular Case Studies
|
October 20, 2021
Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the <i>SLC17A5</i> gene
Afia Hasnain, Sherri Burnett, Ronald Agatep, et al.
Page
of 48
Search research articles
Search
Showing results (361-370 of 479) with videos related to
Sort By:
Page
of 48
Cold Spring Harbor Molecular Case Studies
|
June 22, 2022
Incidental discovery of acute myeloid leukemia during liquid biopsy of a lung cancer patient
Dingani Nkosi, Caroline A Miller, Audrey N Jajosky, et al.
Cold Spring Harbor Molecular Case Studies
|
June 22, 2022
WP1066 induces cell death in a schwannomatosis patient-derived schwannoma cell line
Abdulrahman Allaf, Berta Victoria, Rosa Rosario, et al.
Cold Spring Harbor Molecular Case Studies
|
January 13, 2021
Refractory alveolar rhabdomyosarcoma in an 11-year-old male
Cora A Ricker, Andrew D Woods, William Simonson, et al.
Cold Spring Harbor Molecular Case Studies
|
June 17, 2017
Successful immune checkpoint blockade in a patient with advanced stage microsatellite-unstable biliary tract cancer
Elena Czink, Matthias Kloor, Benjamin Goeppert, et al.
Cold Spring Harbor Molecular Case Studies
|
September 15, 2016
A novel de novo mutation in ATP1A3 and childhood-onset schizophrenia
Niklas Smedemark-Margulies, Catherine A Brownstein, Sigella Vargas, et al.
Cold Spring Harbor Molecular Case Studies
|
September 15, 2016
Testing ERBB2 p.L755S kinase domain mutation as a druggable target in a patient with advanced colorectal cancer
Kyaw L Aung, Tracy L Stockley, Stefano Serra, et al.
Cold Spring Harbor Molecular Case Studies
|
February 12, 2022
Expanding the clinical phenotype of <i>FGFR1</i> internal tandem duplication
Esko A Kautto, Kathleen M Schieffer, Sean McGrath, et al.
Cold Spring Harbor Molecular Case Studies
|
January 29, 2022
Inherited and de novo variants extend the etiology of <i>TAOK1</i>-associated neurodevelopmental disorder
Jesse M Hunter, Lauren J Massingham, Kandamurugu Manickam, et al.
Cold Spring Harbor Molecular Case Studies
|
February 15, 2022
Ethylmalonic encephalopathy masquerading as meningococcemia
Ari Horton, Kai Mun Hong, Dinusha Pandithan, et al.
Cold Spring Harbor Molecular Case Studies
|
October 20, 2021
Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the <i>SLC17A5</i> gene
Afia Hasnain, Sherri Burnett, Ronald Agatep, et al.
Page
of 48