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

Joey Lai-Cheong

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

Pageof 1
Sort By:
The New England Journal of Medicine|December 24, 2010
Images in clinical medicine. TineaJoey Lai-Cheong, John McGrath
Contact Dermatitis|March 21, 2013
Chemical atopyPailin Puangpet, Joey Lai-Cheong, John P McFadden
Anais Brasileiros De Dermatologia|December 19, 2013
Sporadic Kindler syndrome with a novel mutationHiram Larangeira de Almeida, Gláucia Thomas Heckler, Kenneth Fong, et al.
Photodermatology, Photoimmunology & Photomedicine|March 12, 2011
Successful treatment of microstomia with UVA1 phototherapy in systemic sclerosisAngela Tewari, Trish Garibaldinos, Joey Lai-Cheong, et al.
Anais Brasileiros De Dermatologia|September 17, 2015
Is adermatoglyphia an additional feature of Kindler Syndrome?Hiram Larangeira de Almeida, Fernanda Mendes Goetze, Kenneth Fong, et al.
The Journal of Investigative Dermatology|March 18, 2011
cis-Urocanic acid enhances prostaglandin E2 release and apoptotic cell death via reactive oxygen species in human keratinocytesKazuyo Kaneko, Susan L Walker, Joey Lai-Cheong, et al.
Acta Dermato-Venereologica|February 7, 2009
New glycine substitution mutations in type VII collagen underlying epidermolysis bullosa pruriginosa but the phenotype is not explained by a common polymorphism in the matrix metalloproteinase-1 gene promoterNoor Almaani, Lu Liu, Naomi Harrison, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
American Journal of Human Genetics|January 9, 2008
Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosisKen Arita, Andrew P South, Günter Hans-Filho, et al.
European Journal of Human Genetics : EJHG|August 20, 2009
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosisMing-Wei Lin, Ding-Dar Lee, Tze-Tze Liu, et al.
Pageof 1

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

Sort By:
Pageof 1
The New England Journal of Medicine|December 24, 2010
Images in clinical medicine. TineaJoey Lai-Cheong, John McGrath
Contact Dermatitis|March 21, 2013
Chemical atopyPailin Puangpet, Joey Lai-Cheong, John P McFadden
Anais Brasileiros De Dermatologia|December 19, 2013
Sporadic Kindler syndrome with a novel mutationHiram Larangeira de Almeida, Gláucia Thomas Heckler, Kenneth Fong, et al.
Photodermatology, Photoimmunology & Photomedicine|March 12, 2011
Successful treatment of microstomia with UVA1 phototherapy in systemic sclerosisAngela Tewari, Trish Garibaldinos, Joey Lai-Cheong, et al.
Anais Brasileiros De Dermatologia|September 17, 2015
Is adermatoglyphia an additional feature of Kindler Syndrome?Hiram Larangeira de Almeida, Fernanda Mendes Goetze, Kenneth Fong, et al.
The Journal of Investigative Dermatology|March 18, 2011
cis-Urocanic acid enhances prostaglandin E2 release and apoptotic cell death via reactive oxygen species in human keratinocytesKazuyo Kaneko, Susan L Walker, Joey Lai-Cheong, et al.
Acta Dermato-Venereologica|February 7, 2009
New glycine substitution mutations in type VII collagen underlying epidermolysis bullosa pruriginosa but the phenotype is not explained by a common polymorphism in the matrix metalloproteinase-1 gene promoterNoor Almaani, Lu Liu, Naomi Harrison, et al.
Investigative Ophthalmology & Visual Science|February 19, 2010
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular musclesPatrick Yu-Wai-Man, Joey Lai-Cheong, Gillian M Borthwick, et al.
American Journal of Human Genetics|January 9, 2008
Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosisKen Arita, Andrew P South, Günter Hans-Filho, et al.
European Journal of Human Genetics : EJHG|August 20, 2009
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosisMing-Wei Lin, Ding-Dar Lee, Tze-Tze Liu, et al.
Pageof 1