Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michael Field

Showing results (61-70 of 136) with videos related to

Pageof 14
Sort By:
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|June 20, 2006
Comparative field performance over 3 years and two sites of transgenic wheat lines expressing HMW subunit transgenesPeter R Shewry, Stephen Powers, J Michael Field, et al.
Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
The American Journal of Surgical Pathology|August 22, 2022
A Clinicopathologic and Molecular Analysis of Fumarate Hydratase-deficient Pheochromocytoma and ParagangliomaTalia L Fuchs, Catherine Luxford, Adele Clarkson, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
Clinical Chemistry|April 30, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spotsYoshimi Inaba, Charles E Schwartz, Quang M Bui, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 13, 2019
Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.
American Journal of Human Genetics|April 1, 2014
De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disabilityDetelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, et al.
Inflammatory Bowel Diseases|October 17, 2023
Efficacy and Safety of Anti-Tumor Necrosis Factor Alpha in Very Early Onset Inflammatory Bowel DiseaseLauren V Collen, Vanessa Mitsialis, David Y Kim, et al.
Gastroenterology|May 20, 2020
Single-Cell Analyses of Colon and Blood Reveal Distinct Immune Cell Signatures of Ulcerative Colitis and Crohn's DiseaseVanessa Mitsialis, Sarah Wall, Peng Liu, et al.
European Journal of Human Genetics : EJHG|March 31, 2018
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family historyBettina Meiser, Veronica F Quinn, Gillian Mitchell, et al.
Pageof 14

Showing results (61-70 of 136) with videos related to

Sort By:
Pageof 14
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|June 20, 2006
Comparative field performance over 3 years and two sites of transgenic wheat lines expressing HMW subunit transgenesPeter R Shewry, Stephen Powers, J Michael Field, et al.
Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
The American Journal of Surgical Pathology|August 22, 2022
A Clinicopathologic and Molecular Analysis of Fumarate Hydratase-deficient Pheochromocytoma and ParagangliomaTalia L Fuchs, Catherine Luxford, Adele Clarkson, et al.
International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated <i>FMR1</i> mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.
Clinical Chemistry|April 30, 2014
Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spotsYoshimi Inaba, Charles E Schwartz, Quang M Bui, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 13, 2019
Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.
American Journal of Human Genetics|April 1, 2014
De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disabilityDetelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, et al.
Inflammatory Bowel Diseases|October 17, 2023
Efficacy and Safety of Anti-Tumor Necrosis Factor Alpha in Very Early Onset Inflammatory Bowel DiseaseLauren V Collen, Vanessa Mitsialis, David Y Kim, et al.
Gastroenterology|May 20, 2020
Single-Cell Analyses of Colon and Blood Reveal Distinct Immune Cell Signatures of Ulcerative Colitis and Crohn's DiseaseVanessa Mitsialis, Sarah Wall, Peng Liu, et al.
European Journal of Human Genetics : EJHG|March 31, 2018
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family historyBettina Meiser, Veronica F Quinn, Gillian Mitchell, et al.
Pageof 14