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D Nicholls

Showing results (211-220 of 228) with videos related to

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American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Scientific Reports|August 5, 2020
A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromesIgor Ribeiro Ferreira, Régis Afonso Costa, Leonardo Henrique Ferreira Gomes, et al.
The International Journal of Eating Disorders|September 18, 2007
Classification of child and adolescent eating disturbances. Workgroup for Classification of Eating Disorders in Children and Adolescents (WCEDCA)T Bravender, R Bryant-Waugh, D Herzog, et al.
Plos Genetics|April 17, 2023
Insulin secretion deficits in a Prader-Willi syndrome β-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperonesErik A Koppes, Marie A Johnson, James J Moresco, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2016
Functional evolution of IGF2:IGF2R domain 11 binding generates novel structural interactions and a specific IGF2 antagonistSusana Frago, Ryan D Nicholls, Madeleine Strickland, et al.
JMIR Research Protocols|March 18, 2024
Group Acceptance and Commitment Therapy for Recovery From Psychosis: Protocol for a Single-Group Waitlist TrialMarilyn L Cugnetto, Eric M J Morris, Siobain F Bonfield, et al.
European Eating Disorders Review : the Journal of the Eating Disorders Association|February 13, 2010
Classification of eating disturbance in children and adolescents: proposed changes for the DSM-VT Bravender, R Bryant-Waugh, D Herzog, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.
Pageof 23

Showing results (211-220 of 228) with videos related to

Sort By:
Pageof 23
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Report of the Third International Workshop on Human Chromosome 15 Mapping 1996. October 25-27, 1996 in Vancouver B.C., CanadaW P Robinson, B Horsthemke, S Leonard, et al.
Scientific Reports|August 5, 2020
A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromesIgor Ribeiro Ferreira, Régis Afonso Costa, Leonardo Henrique Ferreira Gomes, et al.
The International Journal of Eating Disorders|September 18, 2007
Classification of child and adolescent eating disturbances. Workgroup for Classification of Eating Disorders in Children and Adolescents (WCEDCA)T Bravender, R Bryant-Waugh, D Herzog, et al.
Plos Genetics|April 17, 2023
Insulin secretion deficits in a Prader-Willi syndrome β-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperonesErik A Koppes, Marie A Johnson, James J Moresco, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2016
Functional evolution of IGF2:IGF2R domain 11 binding generates novel structural interactions and a specific IGF2 antagonistSusana Frago, Ryan D Nicholls, Madeleine Strickland, et al.
JMIR Research Protocols|March 18, 2024
Group Acceptance and Commitment Therapy for Recovery From Psychosis: Protocol for a Single-Group Waitlist TrialMarilyn L Cugnetto, Eric M J Morris, Siobain F Bonfield, et al.
European Eating Disorders Review : the Journal of the Eating Disorders Association|February 13, 2010
Classification of eating disturbance in children and adolescents: proposed changes for the DSM-VT Bravender, R Bryant-Waugh, D Herzog, et al.
Scientific Reports|December 24, 2025
Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndromeShokouh Shahrokhi, Emma K Baker, Michael See, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.
Pageof 23