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Maranke I Koster

Showing results (31-40 of 53) with videos related to

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Developmental Biology|March 21, 2008
Disruption of epidermal specific gene expression and delayed skin development in AP-2 gamma mutant miceJillian Guttormsen, Maranke I Koster, John R Stevens, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
p63 induces key target genes required for epidermal morphogenesisMaranke I Koster, Daisy Dai, Barbara Marinari, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
DeltaNp63 knockdown mice: A mouse model for AEC syndromeMaranke I Koster, Barbara Marinari, Aimee S Payne, et al.
ACS Nano|September 22, 2020
Solar Freckles: Long-Term Photochromic Tattoos for Intradermal Ultraviolet RadiometryJesse L Butterfield, Sean P Keyser, Karan V Dikshit, et al.
American Journal of Medical Genetics. Part A|October 15, 2025
Complex Wounds in Ectodermal Dysplasias: Translating Discovery to TherapyMary Fete, Becky M Abbott, Maddison N Salois, et al.
Plos One|December 11, 2012
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosisJianning Tao, Maranke I Koster, Wilbur Harrison, et al.
Fetal and Pediatric Pathology|April 18, 2024
Immunohistochemical and Histopathological Characterization of Spina Bifida Defect Tissues Removed After Prenatal and Postnatal Surgical RepairJames R Bardill, Melissa R Laughter, Jaclyn B Anderson, et al.
Genesis (New York, N.Y. : 2000)|April 10, 2007
Double-inducible gene activation system for caspase 3 and 9 in epidermisViraj R Shah, Maranke I Koster, Dennis R Roop, et al.
The Journal of Investigative Dermatology|February 27, 2018
A Human Stem Cell-Based System to Study the Role of TP63 Mutations in Ectodermal DysplasiasJason D Dinella, Jiangli Chen, Saiphone Webb, et al.
American Journal of Medical Genetics. Part A|December 19, 2022
Rare diseases of ectoderm: Translating discovery to therapyJohn Timothy Wright, Becky M Abbott, Maddison N Salois, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Developmental Biology|March 21, 2008
Disruption of epidermal specific gene expression and delayed skin development in AP-2 gamma mutant miceJillian Guttormsen, Maranke I Koster, John R Stevens, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
p63 induces key target genes required for epidermal morphogenesisMaranke I Koster, Daisy Dai, Barbara Marinari, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
DeltaNp63 knockdown mice: A mouse model for AEC syndromeMaranke I Koster, Barbara Marinari, Aimee S Payne, et al.
ACS Nano|September 22, 2020
Solar Freckles: Long-Term Photochromic Tattoos for Intradermal Ultraviolet RadiometryJesse L Butterfield, Sean P Keyser, Karan V Dikshit, et al.
American Journal of Medical Genetics. Part A|October 15, 2025
Complex Wounds in Ectodermal Dysplasias: Translating Discovery to TherapyMary Fete, Becky M Abbott, Maddison N Salois, et al.
Plos One|December 11, 2012
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosisJianning Tao, Maranke I Koster, Wilbur Harrison, et al.
Fetal and Pediatric Pathology|April 18, 2024
Immunohistochemical and Histopathological Characterization of Spina Bifida Defect Tissues Removed After Prenatal and Postnatal Surgical RepairJames R Bardill, Melissa R Laughter, Jaclyn B Anderson, et al.
Genesis (New York, N.Y. : 2000)|April 10, 2007
Double-inducible gene activation system for caspase 3 and 9 in epidermisViraj R Shah, Maranke I Koster, Dennis R Roop, et al.
The Journal of Investigative Dermatology|February 27, 2018
A Human Stem Cell-Based System to Study the Role of TP63 Mutations in Ectodermal DysplasiasJason D Dinella, Jiangli Chen, Saiphone Webb, et al.
American Journal of Medical Genetics. Part A|December 19, 2022
Rare diseases of ectoderm: Translating discovery to therapyJohn Timothy Wright, Becky M Abbott, Maddison N Salois, et al.
Pageof 6