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 Platt

Showing results (441-450 of 505) with videos related to

Pageof 51
Sort By:
Wellcome Open Research|June 13, 2022
Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type CIsabelle Williams, Sumeet Pandey, Wolfram Haller, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 29, 2015
Collecting lymphatic vessel permeability facilitates adipose tissue inflammation and distribution of antigen to lymph node-homing adipose tissue dendritic cellsEmma L Kuan, Stoyan Ivanov, Eric A Bridenbaugh, et al.
Journal of Geophysical Research. Atmospheres : JGR|March 7, 2017
Constraints on oceanic methane emissions west of Svalbard from atmospheric in situ measurements and Lagrangian transport modelingI Pisso, C Lund Myhre, S M Platt, et al.
Nature Genetics|October 27, 2004
Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthaseMichael A Simpson, Harold Cross, Christos Proukakis, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapyF M Platt, M Jeyakumar, U Andersson, et al.
The Journal of Clinical Investigation|February 24, 2022
CADASIL mutations sensitize the brain to ischemia via spreading depolarizations and abnormal extracellular potassium homeostasisFumiaki Oka, Jeong Hyun Lee, Izumi Yuzawa, et al.
Orphanet Journal of Rare Diseases|October 29, 2025
Glycoprotein non-metastatic melanoma protein B is a biomarker of inflammation in individuals with Gaucher disease: relationship to clinico-pathological subtypesSebile Kilavuz, Kerri-Lee Wallom, Ana Catarina Gomes Almeida Augusto Caçote, et al.
Plos One|August 31, 2021
Correction: Molecular basis for a new bovine model of Niemann-Pick type C diseaseShernae A Woolley, Emily R Tsimnadis, Cor Lenghaus, et al.
Biochimica Et Biophysica Acta|June 29, 2015
Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorderInés Adriana Cismondi, Romina Kohan, Heather Adams, et al.
Wellcome Open Research|April 18, 2023
Defective iron homeostasis and hematological abnormalities in Niemann-Pick disease type C1Oscar C W Chen, Stephan Siebel, Alexandria Colaco, et al.
Pageof 51

Showing results (441-450 of 505) with videos related to

Sort By:
Pageof 51
Wellcome Open Research|June 13, 2022
Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type CIsabelle Williams, Sumeet Pandey, Wolfram Haller, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 29, 2015
Collecting lymphatic vessel permeability facilitates adipose tissue inflammation and distribution of antigen to lymph node-homing adipose tissue dendritic cellsEmma L Kuan, Stoyan Ivanov, Eric A Bridenbaugh, et al.
Journal of Geophysical Research. Atmospheres : JGR|March 7, 2017
Constraints on oceanic methane emissions west of Svalbard from atmospheric in situ measurements and Lagrangian transport modelingI Pisso, C Lund Myhre, S M Platt, et al.
Nature Genetics|October 27, 2004
Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthaseMichael A Simpson, Harold Cross, Christos Proukakis, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapyF M Platt, M Jeyakumar, U Andersson, et al.
The Journal of Clinical Investigation|February 24, 2022
CADASIL mutations sensitize the brain to ischemia via spreading depolarizations and abnormal extracellular potassium homeostasisFumiaki Oka, Jeong Hyun Lee, Izumi Yuzawa, et al.
Orphanet Journal of Rare Diseases|October 29, 2025
Glycoprotein non-metastatic melanoma protein B is a biomarker of inflammation in individuals with Gaucher disease: relationship to clinico-pathological subtypesSebile Kilavuz, Kerri-Lee Wallom, Ana Catarina Gomes Almeida Augusto Caçote, et al.
Plos One|August 31, 2021
Correction: Molecular basis for a new bovine model of Niemann-Pick type C diseaseShernae A Woolley, Emily R Tsimnadis, Cor Lenghaus, et al.
Biochimica Et Biophysica Acta|June 29, 2015
Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorderInés Adriana Cismondi, Romina Kohan, Heather Adams, et al.
Wellcome Open Research|April 18, 2023
Defective iron homeostasis and hematological abnormalities in Niemann-Pick disease type C1Oscar C W Chen, Stephan Siebel, Alexandria Colaco, et al.
Pageof 51