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William Allen

Showing results (41-50 of 55) with videos related to

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American Journal of Medical Genetics. Part A|June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndromeKaren W Gripp, Angela E Lin, Linda Nicholson, et al.
Human Molecular Genetics|May 28, 2021
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disordersLinda M Reis, Elena A Sorokina, Lubica Dudakova, et al.
Med (New York, N.Y.)|May 19, 2022
Liquid biopsies for residual disease and recurrenceJonathan Chee Ming Wan, Tariq Imdadali Mughal, Pedram Razavi, et al.
Cell Reports|October 3, 2025
Targeting an essential viral oncoprotein with an IL-7-enhanced mRNA vaccine induces durable immunity to Merkel cell carcinomaAlexander Frey, Kathryn Clulo, Yuewei Fei, et al.
Human Molecular Genetics|April 4, 2017
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expressionLise-Marie Donnio, Baptiste Bidon, Satoru Hashimoto, et al.
Transfusion|January 28, 2023
Storage differentially impacts alloimmunization to distinct red cell antigens following transfusion in miceCheryl L Maier, Ryan P Jajosky, Seema R Patel, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Toriello-Carey syndrome: delineation and reviewHelga V Toriello, John C Carey, Marie-Claude Addor, et al.
Nature Communications|October 2, 2020
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Molecular Genetics and Metabolism|July 14, 2022
Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosisChristina Nießl, Anne-Laure Boulesteix, Jun Oh, et al.
Nature Communications|September 16, 2020
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndromeKaren W Gripp, Angela E Lin, Linda Nicholson, et al.
Human Molecular Genetics|May 28, 2021
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disordersLinda M Reis, Elena A Sorokina, Lubica Dudakova, et al.
Med (New York, N.Y.)|May 19, 2022
Liquid biopsies for residual disease and recurrenceJonathan Chee Ming Wan, Tariq Imdadali Mughal, Pedram Razavi, et al.
Cell Reports|October 3, 2025
Targeting an essential viral oncoprotein with an IL-7-enhanced mRNA vaccine induces durable immunity to Merkel cell carcinomaAlexander Frey, Kathryn Clulo, Yuewei Fei, et al.
Human Molecular Genetics|April 4, 2017
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expressionLise-Marie Donnio, Baptiste Bidon, Satoru Hashimoto, et al.
Transfusion|January 28, 2023
Storage differentially impacts alloimmunization to distinct red cell antigens following transfusion in miceCheryl L Maier, Ryan P Jajosky, Seema R Patel, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Toriello-Carey syndrome: delineation and reviewHelga V Toriello, John C Carey, Marie-Claude Addor, et al.
Nature Communications|October 2, 2020
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Molecular Genetics and Metabolism|July 14, 2022
Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosisChristina Nießl, Anne-Laure Boulesteix, Jun Oh, et al.
Nature Communications|September 16, 2020
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.
Pageof 6