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K Armstrong

Showing results (1021-1030 of 1,035) with videos related to

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Carcinogenesis|July 2, 2014
Identification of a melanoma susceptibility locus and somatic mutation in TET2Fengju Song, Christopher I Amos, Jeffrey E Lee, et al.
American Journal of Human Genetics|May 21, 2026
Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assemblyRobin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar, et al.
Nature Genetics|May 20, 2008
Common sequence variants on 20q11.22 confer melanoma susceptibilityKevin M Brown, Stuart Macgregor, Grant W Montgomery, et al.
Science (New York, N.Y.)|June 10, 2017
Mismatch repair deficiency predicts response of solid tumors to PD-1 blockadeDung T Le, Jennifer N Durham, Kellie N Smith, et al.
Nature|November 15, 2011
A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaSatoru Yokoyama, Susan L Woods, Glen M Boyle, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3Stuart Macgregor, Grant W Montgomery, Jimmy Z Liu, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 4, 2020
ACC/AHA/ASE/HRS/ISACHD/SCAI/SCCT/SCMR/SOPE 2020 Appropriate Use Criteria for Multimodality Imaging During the Follow-Up Care of Patients With Congenital Heart Disease: A Report of the American College of Cardiology Solution Set Oversight Committee and Appropriate Use Criteria Task Force, American Heart Association, American Society of Echocardiography, Heart Rhythm Society, International Society for Adult Congenital Heart Disease, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, Society for Cardiovascular Magnetic Resonance, and Society of Pediatric Echocardiography, Ritu Sachdeva, Anne Marie Valente, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies three new melanoma susceptibility lociJennifer H Barrett, Mark M Iles, Mark Harland, et al.
The Lancet. Respiratory Medicine|July 8, 2015
Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trialEric W F W Alton, David K Armstrong, Deborah Ashby, et al.
Journal of the National Cancer Institute. Monographs|September 1, 2014
Etiologic heterogeneity among non-Hodgkin lymphoma subtypes: the InterLymph Non-Hodgkin Lymphoma Subtypes ProjectLindsay M Morton, Susan L Slager, James R Cerhan, et al.
Pageof 104

Showing results (1021-1030 of 1,035) with videos related to

Sort By:
Pageof 104
Carcinogenesis|July 2, 2014
Identification of a melanoma susceptibility locus and somatic mutation in TET2Fengju Song, Christopher I Amos, Jeffrey E Lee, et al.
American Journal of Human Genetics|May 21, 2026
Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assemblyRobin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar, et al.
Nature Genetics|May 20, 2008
Common sequence variants on 20q11.22 confer melanoma susceptibilityKevin M Brown, Stuart Macgregor, Grant W Montgomery, et al.
Science (New York, N.Y.)|June 10, 2017
Mismatch repair deficiency predicts response of solid tumors to PD-1 blockadeDung T Le, Jennifer N Durham, Kellie N Smith, et al.
Nature|November 15, 2011
A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaSatoru Yokoyama, Susan L Woods, Glen M Boyle, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3Stuart Macgregor, Grant W Montgomery, Jimmy Z Liu, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 4, 2020
ACC/AHA/ASE/HRS/ISACHD/SCAI/SCCT/SCMR/SOPE 2020 Appropriate Use Criteria for Multimodality Imaging During the Follow-Up Care of Patients With Congenital Heart Disease: A Report of the American College of Cardiology Solution Set Oversight Committee and Appropriate Use Criteria Task Force, American Heart Association, American Society of Echocardiography, Heart Rhythm Society, International Society for Adult Congenital Heart Disease, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, Society for Cardiovascular Magnetic Resonance, and Society of Pediatric Echocardiography, Ritu Sachdeva, Anne Marie Valente, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies three new melanoma susceptibility lociJennifer H Barrett, Mark M Iles, Mark Harland, et al.
The Lancet. Respiratory Medicine|July 8, 2015
Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trialEric W F W Alton, David K Armstrong, Deborah Ashby, et al.
Journal of the National Cancer Institute. Monographs|September 1, 2014
Etiologic heterogeneity among non-Hodgkin lymphoma subtypes: the InterLymph Non-Hodgkin Lymphoma Subtypes ProjectLindsay M Morton, Susan L Slager, James R Cerhan, et al.
Pageof 104