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

M Maier

Showing results (821-830 of 863) with videos related to

Pageof 87
Sort By:
Plos One|July 14, 2010
Identification, characterization and immunogenicity of an O-antigen capsular polysaccharide of Francisella tularensisMichael A Apicella, Deborah M B Post, Andrew C Fowler, et al.
Journal of Inherited Metabolic Disease|November 18, 2016
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revisionNikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Plos Genetics|January 3, 2009
IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor productionLisa M Maier, Christopher E Lowe, Jason Cooper, et al.
Journal of Clinical Apheresis|September 17, 2020
Terumo spectra optia leukapheresis of cynomolgus macaques for hematopoietic stem cell and T cell collectionHelen L Wu, Justin M Greene, Tonya Swanson, et al.
Genes and Immunity|October 31, 2008
CD226 Gly307Ser association with multiple autoimmune diseasesJ P Hafler, L M Maier, J D Cooper, et al.
Nature|November 16, 2007
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-ASergey Nejentsev, Joanna M M Howson, Neil M Walker, et al.
Orphanet Journal of Rare Diseases|November 24, 2020
Clinical disease progression and biomarkers in Niemann-Pick disease type C: a prospective cohort studyEugen Mengel, Bruno Bembi, Mireia Del Toro, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2025
Mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency: From metabolism to clinical implicationsSarah C Grünert, Matthias R Baumgartner, Juliette Bouchereau, et al.
Physical Review Letters|May 1, 2001
Measurement of the resonant d(mu)t molecular formation rate in solid HDT A Porcelli, A Adamczak, J M Bailey, et al.
Nature Genetics|October 18, 2005
Population structure, differential bias and genomic control in a large-scale, case-control association studyDavid G Clayton, Neil M Walker, Deborah J Smyth, et al.
Pageof 87

Showing results (821-830 of 863) with videos related to

Sort By:
Pageof 87
Plos One|July 14, 2010
Identification, characterization and immunogenicity of an O-antigen capsular polysaccharide of Francisella tularensisMichael A Apicella, Deborah M B Post, Andrew C Fowler, et al.
Journal of Inherited Metabolic Disease|November 18, 2016
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revisionNikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Plos Genetics|January 3, 2009
IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor productionLisa M Maier, Christopher E Lowe, Jason Cooper, et al.
Journal of Clinical Apheresis|September 17, 2020
Terumo spectra optia leukapheresis of cynomolgus macaques for hematopoietic stem cell and T cell collectionHelen L Wu, Justin M Greene, Tonya Swanson, et al.
Genes and Immunity|October 31, 2008
CD226 Gly307Ser association with multiple autoimmune diseasesJ P Hafler, L M Maier, J D Cooper, et al.
Nature|November 16, 2007
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-ASergey Nejentsev, Joanna M M Howson, Neil M Walker, et al.
Orphanet Journal of Rare Diseases|November 24, 2020
Clinical disease progression and biomarkers in Niemann-Pick disease type C: a prospective cohort studyEugen Mengel, Bruno Bembi, Mireia Del Toro, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 14, 2025
Mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency: From metabolism to clinical implicationsSarah C Grünert, Matthias R Baumgartner, Juliette Bouchereau, et al.
Physical Review Letters|May 1, 2001
Measurement of the resonant d(mu)t molecular formation rate in solid HDT A Porcelli, A Adamczak, J M Bailey, et al.
Nature Genetics|October 18, 2005
Population structure, differential bias and genomic control in a large-scale, case-control association studyDavid G Clayton, Neil M Walker, Deborah J Smyth, et al.
Pageof 87