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Rachel Harrison

Showing results (51-60 of 65) with videos related to

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Journal of Neuroinflammation|August 25, 2009
Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's diseaseOnofre Combarros, Cornelia M van Duijn, Naomi Hammond, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 22, 2025
Evaluating the return of additional findings from the 100,000 Genomes Project: A mixed methods study exploring participant experiences of receiving secondary findings from genomic sequencingBethany Stafford-Smith, Morgan Daniel, Michelle Peter, et al.
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Placenta accreta spectrum care infrastructure: an evidence-based review of needed resources supporting placenta accreta spectrum careGarrett D Fitzgerald, J M Newton, Lamia Atasi, et al.
Clinical Endocrinology|September 24, 2021
SDHC phaeochromocytoma and paraganglioma: A UK-wide case seriesSophie T Williams, Prodromos Chatzikyriakou, Paul V Carroll, et al.
Molecular Cancer Therapeutics|November 8, 2006
Mutation analysis of 24 known cancer genes in the NCI-60 cell line setOgechi N Ikediobi, Helen Davies, Graham Bignell, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Genes, Chromosomes & Cancer|September 22, 2005
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adultsGraham Bignell, Raffaella Smith, Chris Hunter, et al.
Cancer Research|April 19, 2006
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyChris Hunter, Raffaella Smith, Daniel P Cahill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Journal of Neuroinflammation|August 25, 2009
Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's diseaseOnofre Combarros, Cornelia M van Duijn, Naomi Hammond, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 22, 2025
Evaluating the return of additional findings from the 100,000 Genomes Project: A mixed methods study exploring participant experiences of receiving secondary findings from genomic sequencingBethany Stafford-Smith, Morgan Daniel, Michelle Peter, et al.
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Placenta accreta spectrum care infrastructure: an evidence-based review of needed resources supporting placenta accreta spectrum careGarrett D Fitzgerald, J M Newton, Lamia Atasi, et al.
Clinical Endocrinology|September 24, 2021
SDHC phaeochromocytoma and paraganglioma: A UK-wide case seriesSophie T Williams, Prodromos Chatzikyriakou, Paul V Carroll, et al.
Molecular Cancer Therapeutics|November 8, 2006
Mutation analysis of 24 known cancer genes in the NCI-60 cell line setOgechi N Ikediobi, Helen Davies, Graham Bignell, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
American Journal of Human Genetics|January 20, 2007
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorPatrick S Tarpey, F Lucy Raymond, Sarah O'Meara, et al.
Genes, Chromosomes & Cancer|September 22, 2005
Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adultsGraham Bignell, Raffaella Smith, Chris Hunter, et al.
Cancer Research|April 19, 2006
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapyChris Hunter, Raffaella Smith, Daniel P Cahill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Pageof 7