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Therapeutic Advances in Medical Oncology
|
December 5, 2019
KRAS and ERBB-family genetic alterations affect response to PD-1 inhibitors in metastatic nonsquamous NSCLC
Marika Cinausero, Noemi Laprovitera, Giovanna De Maglio, et al.
Thrombosis and Haemostasis
|
December 21, 2019
Particulate Shiga Toxin 2 in Blood is Associated to the Development of Hemolytic Uremic Syndrome in Children
Maurizio Brigotti, Xiaohua He, Domenica Carnicelli, et al.
Molecular Oncology
|
June 2, 2021
MicroRNA expression profiling with a droplet digital PCR assay enables molecular diagnosis and prognosis of cancers of unknown primary
Noemi Laprovitera, Mattia Riefolo, Elisa Porcellini, et al.
Cellular Microbiology
|
December 23, 2018
The structure of the Shiga toxin 2a A-subunit dictates the interactions of the toxin with blood components
Maurizio Brigotti, Dorothea Orth-Höller, Domenica Carnicelli, et al.
Iscience
|
July 31, 2025
An antibiotic derivative as a new potential tool in the prevention of hemolytic uremic syndrome
Elisa Varrone, Luciano Consagra, Domenica Carnicelli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 21, 2024
Synergic activity of FGFR2 and MEK inhibitors in the treatment of FGFR2-amplified cancers of unknown primary
Andrea Cavazzoni, Irene Salamon, Claudia Fumarola, et al.
Neurobiology of Aging
|
January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations
Jean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-Charles Lambert, Simon Heath, Gael Even, et al.
Journal of Alzheimer'S Disease : JAD
|
September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study
Jean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Nature Genetics
|
April 5, 2011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Paul Hollingworth, Denise Harold, Rebecca Sims, et al.
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of 5
Search research articles
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Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
Therapeutic Advances in Medical Oncology
|
December 5, 2019
KRAS and ERBB-family genetic alterations affect response to PD-1 inhibitors in metastatic nonsquamous NSCLC
Marika Cinausero, Noemi Laprovitera, Giovanna De Maglio, et al.
Thrombosis and Haemostasis
|
December 21, 2019
Particulate Shiga Toxin 2 in Blood is Associated to the Development of Hemolytic Uremic Syndrome in Children
Maurizio Brigotti, Xiaohua He, Domenica Carnicelli, et al.
Molecular Oncology
|
June 2, 2021
MicroRNA expression profiling with a droplet digital PCR assay enables molecular diagnosis and prognosis of cancers of unknown primary
Noemi Laprovitera, Mattia Riefolo, Elisa Porcellini, et al.
Cellular Microbiology
|
December 23, 2018
The structure of the Shiga toxin 2a A-subunit dictates the interactions of the toxin with blood components
Maurizio Brigotti, Dorothea Orth-Höller, Domenica Carnicelli, et al.
Iscience
|
July 31, 2025
An antibiotic derivative as a new potential tool in the prevention of hemolytic uremic syndrome
Elisa Varrone, Luciano Consagra, Domenica Carnicelli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 21, 2024
Synergic activity of FGFR2 and MEK inhibitors in the treatment of FGFR2-amplified cancers of unknown primary
Andrea Cavazzoni, Irene Salamon, Claudia Fumarola, et al.
Neurobiology of Aging
|
January 12, 2011
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations
Jean-Charles Lambert, Diana Zelenika, Mikko Hiltunen, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-Charles Lambert, Simon Heath, Gael Even, et al.
Journal of Alzheimer'S Disease : JAD
|
September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study
Jean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Nature Genetics
|
April 5, 2011
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Paul Hollingworth, Denise Harold, Rebecca Sims, et al.
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of 5