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

Peter Budd

Showing results (1-10 of 7) with videos related to

Pageof 1
Sort By:
Scientific Reports|August 9, 2016
Enhanced gas separation factors of microporous polymer constrained in the channels of anodic alumina membranesEkaterina Chernova, Dmitrii Petukhov, Olga Boytsova, et al.
Pigment Cell & Melanoma Research|May 13, 2025
A Dominant Mutation in G<sub>α</sub>s-Protein Increases Hair PigmentationPhilip S Goff, Peter Budd, Darren W Logan, et al.
Membranes|January 21, 2022
Novel Mixed Matrix Membranes Based on Polymer of Intrinsic Microporosity PIM-1 Modified with Metal-Organic Frameworks for Removal of Heavy Metal Ions and Food Dyes by NanofiltrationAnna Kuzminova, Mariia Dmitrenko, Andrey Zolotarev, et al.
Pigment Cell & Melanoma Research|November 22, 2022
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineageEmma L Wilkinson, Louise C Brennan, Olivia J Harrison, et al.
The Journal of Investigative Dermatology|May 11, 2012
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentVeronica A Kinsler, Sayeda Abu-Amero, Peter Budd, et al.
American Journal of Human Genetics|April 9, 2011
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisPleasantine Mill, Paul J Lockhart, Elizabeth Fitzpatrick, et al.
American Journal of Human Genetics|April 18, 2017
PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic ProteinsEmma A Hall, Michael S Nahorski, Lyndsay M Murray, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Scientific Reports|August 9, 2016
Enhanced gas separation factors of microporous polymer constrained in the channels of anodic alumina membranesEkaterina Chernova, Dmitrii Petukhov, Olga Boytsova, et al.
Pigment Cell & Melanoma Research|May 13, 2025
A Dominant Mutation in G<sub>α</sub>s-Protein Increases Hair PigmentationPhilip S Goff, Peter Budd, Darren W Logan, et al.
Membranes|January 21, 2022
Novel Mixed Matrix Membranes Based on Polymer of Intrinsic Microporosity PIM-1 Modified with Metal-Organic Frameworks for Removal of Heavy Metal Ions and Food Dyes by NanofiltrationAnna Kuzminova, Mariia Dmitrenko, Andrey Zolotarev, et al.
Pigment Cell & Melanoma Research|November 22, 2022
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineageEmma L Wilkinson, Louise C Brennan, Olivia J Harrison, et al.
The Journal of Investigative Dermatology|May 11, 2012
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentVeronica A Kinsler, Sayeda Abu-Amero, Peter Budd, et al.
American Journal of Human Genetics|April 9, 2011
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisPleasantine Mill, Paul J Lockhart, Elizabeth Fitzpatrick, et al.
American Journal of Human Genetics|April 18, 2017
PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic ProteinsEmma A Hall, Michael S Nahorski, Lyndsay M Murray, et al.
Pageof 1