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JAMA Dermatology
|
April 10, 2024
Guselkumab for Pityriasis Rubra Pilaris and Dysregulation of IL-23/IL-17 and NFkB Signaling: A Nonrandomized Trial
Rose C Velasco, Connie Shao, Brett Cutler, et al.
American Journal of Medical Genetics. Part A
|
January 14, 2026
Novel RNF113A Variant Underlying X-Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
Rachel Rabin, Kevin T A Booth, Shawn E Cowper, et al.
BMC Medical Genetics
|
May 5, 2016
Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report
Viviana Karina Dalamón, Paula Buonfiglio, Margarita Larralde, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 26, 2002
KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein
Murat Gunel, Maxwell S H Laurans, Dana Shin, et al.
Developmental Cell
|
January 1, 2019
Single-Cell Analysis Reveals a Hair Follicle Dermal Niche Molecular Differentiation Trajectory that Begins Prior to Morphogenesis
Khusali Gupta, Jonathan Levinsohn, George Linderman, et al.
Cancers
|
January 21, 2022
Introduction of Mutant GNAQ into Endothelial Cells Induces a Vascular Malformation Phenotype with Therapeutic Response to Imatinib
Maiko Sasaki, Yoonhee Jung, Paula North, et al.
JAMA Dermatology
|
April 16, 2020
Evaluation of Ixekizumab Treatment for Patients With Pityriasis Rubra Pilaris: A Single-Arm Trial
Dylan Haynes, Jennifer L Strunck, Christina A Topham, et al.
JAMA Dermatology
|
January 8, 2015
Cellular basis of secondary infections and impaired desquamation in certain inherited ichthyoses
Aegean Chan, Elena Godoy-Gijon, Almudena Nuno-Gonzalez, et al.
The Journal of Investigative Dermatology
|
April 12, 2026
Tape strips capture immune and epidermal hyperplasia markers in the major orphan ichthyoses
Madeline Kim, Meredith Manson, Ying Liu, et al.
EMBO Molecular Medicine
|
July 26, 2024
Dantrolene corrects cellular disease features of Darier disease and may be a novel treatment
Matthew Hunt, Nuoqi Wang, Naricha Pupinyo, et al.
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Search research articles
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Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 4
JAMA Dermatology
|
April 10, 2024
Guselkumab for Pityriasis Rubra Pilaris and Dysregulation of IL-23/IL-17 and NFkB Signaling: A Nonrandomized Trial
Rose C Velasco, Connie Shao, Brett Cutler, et al.
American Journal of Medical Genetics. Part A
|
January 14, 2026
Novel RNF113A Variant Underlying X-Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
Rachel Rabin, Kevin T A Booth, Shawn E Cowper, et al.
BMC Medical Genetics
|
May 5, 2016
Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report
Viviana Karina Dalamón, Paula Buonfiglio, Margarita Larralde, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 26, 2002
KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein
Murat Gunel, Maxwell S H Laurans, Dana Shin, et al.
Developmental Cell
|
January 1, 2019
Single-Cell Analysis Reveals a Hair Follicle Dermal Niche Molecular Differentiation Trajectory that Begins Prior to Morphogenesis
Khusali Gupta, Jonathan Levinsohn, George Linderman, et al.
Cancers
|
January 21, 2022
Introduction of Mutant GNAQ into Endothelial Cells Induces a Vascular Malformation Phenotype with Therapeutic Response to Imatinib
Maiko Sasaki, Yoonhee Jung, Paula North, et al.
JAMA Dermatology
|
April 16, 2020
Evaluation of Ixekizumab Treatment for Patients With Pityriasis Rubra Pilaris: A Single-Arm Trial
Dylan Haynes, Jennifer L Strunck, Christina A Topham, et al.
JAMA Dermatology
|
January 8, 2015
Cellular basis of secondary infections and impaired desquamation in certain inherited ichthyoses
Aegean Chan, Elena Godoy-Gijon, Almudena Nuno-Gonzalez, et al.
The Journal of Investigative Dermatology
|
April 12, 2026
Tape strips capture immune and epidermal hyperplasia markers in the major orphan ichthyoses
Madeline Kim, Meredith Manson, Ying Liu, et al.
EMBO Molecular Medicine
|
July 26, 2024
Dantrolene corrects cellular disease features of Darier disease and may be a novel treatment
Matthew Hunt, Nuoqi Wang, Naricha Pupinyo, et al.
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of 4