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Deeann Wallis

Showing results (11-20 of 37) with videos related to

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Journal of the National Cancer Institute|October 9, 2024
Precision preclinical modeling to advance cancer treatmentDavid H Gutmann, Jesse S Boehm, Elinor K Karlsson, et al.
Human Mutation|October 25, 2021
Analysis of patient-specific NF1 variants leads to functional insights for Ras signaling that can impact personalized medicineAshlee Long, Hui Liu, Jian Liu, et al.
Human Molecular Genetics|September 13, 2015
Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic responseFrédérique Larroquette, Lesley Seto, Perrine L Gaub, et al.
Proteomics|March 26, 2019
Multi-Omics Profiling for NF1 Target Discovery in Neurofibromin (NF1) Deficient CellsRachel M Carnes, James A Mobley, David K Crossman, et al.
Brain Research|May 12, 2012
Initial characterization of mice null for Lphn3, a gene implicated in ADHD and addictionDeeann Wallis, Denise S Hill, Ian A Mendez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibilitySabina Domené, Horia Stanescu, Deeann Wallis, et al.
Journal of Personalized Medicine|December 24, 2021
Restoration of Normal NF1 Function with Antisense Morpholino Treatment of Recurrent Pathogenic Patient-Specific Variant c.1466A>G; p.Y489CElias K Awad, Marc Moore, Hui Liu, et al.
Plos One|April 9, 2015
Functional genomics screening utilizing mutant mouse embryonic stem cells identifies novel radiation-response genesKimberly Loesch, Stacy Galaviz, Zaher Hamoui, et al.
Journal of Pediatric Psychology|March 10, 2006
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effectsHeather F Russell, Deeann Wallis, Michèle M M Mazzocco, et al.
Human Mutation|March 10, 2018
Neurofibromin (NF1) genetic variant structure-function analyses using a full-length mouse cDNADeeann Wallis, Kairong Li, Hui Lui, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Journal of the National Cancer Institute|October 9, 2024
Precision preclinical modeling to advance cancer treatmentDavid H Gutmann, Jesse S Boehm, Elinor K Karlsson, et al.
Human Mutation|October 25, 2021
Analysis of patient-specific NF1 variants leads to functional insights for Ras signaling that can impact personalized medicineAshlee Long, Hui Liu, Jian Liu, et al.
Human Molecular Genetics|September 13, 2015
Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic responseFrédérique Larroquette, Lesley Seto, Perrine L Gaub, et al.
Proteomics|March 26, 2019
Multi-Omics Profiling for NF1 Target Discovery in Neurofibromin (NF1) Deficient CellsRachel M Carnes, James A Mobley, David K Crossman, et al.
Brain Research|May 12, 2012
Initial characterization of mice null for Lphn3, a gene implicated in ADHD and addictionDeeann Wallis, Denise S Hill, Ian A Mendez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibilitySabina Domené, Horia Stanescu, Deeann Wallis, et al.
Journal of Personalized Medicine|December 24, 2021
Restoration of Normal NF1 Function with Antisense Morpholino Treatment of Recurrent Pathogenic Patient-Specific Variant c.1466A>G; p.Y489CElias K Awad, Marc Moore, Hui Liu, et al.
Plos One|April 9, 2015
Functional genomics screening utilizing mutant mouse embryonic stem cells identifies novel radiation-response genesKimberly Loesch, Stacy Galaviz, Zaher Hamoui, et al.
Journal of Pediatric Psychology|March 10, 2006
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effectsHeather F Russell, Deeann Wallis, Michèle M M Mazzocco, et al.
Human Mutation|March 10, 2018
Neurofibromin (NF1) genetic variant structure-function analyses using a full-length mouse cDNADeeann Wallis, Kairong Li, Hui Lui, et al.
Pageof 4