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D Hohl

Showing results (111-120 of 144) with videos related to

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Cell|June 15, 1990
Identification of a major keratinocyte cell envelope protein, loricrinT Mehrel, D Hohl, J A Rothnagel, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 30, 2022
PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndromeG Blanchard, A A Yurchenko, O T Pop, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 6, 2016
Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screeningL Marquardt, M Lacour, M Hoernes, et al.
The British Journal of Dermatology|July 2, 2009
Incidence of bullous pemphigoid and pemphigus in Switzerland: a 2-year prospective studyG Marazza, H C Pham, L Schärer, et al.
The British Journal of Dermatology|March 5, 2014
New and recurrent AAGAB mutations in punctate palmoplantar keratodermaE Pohler, M Huber, S E Boonen, et al.
Current Oncology (Toronto, Ont.)|April 21, 2022
Operationalizing Leadership and Clinician Buy-In to Implement Evidence-Based Tobacco Treatment Programs in Routine Oncology Care: A Mixed-Method Study of the U.S. Cancer Center Cessation InitiativeSarah D Hohl, Jennifer E Bird, Claire V T Nguyen, et al.
Journal of Clinical and Translational Science|January 10, 2025
The intersection of community engagement and team science research: A scoping reviewSarah D Hohl, Erin Abu-Rish Blakeney, Lori Carter-Edwards, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activityE Petit, M Huber, A Rochat, et al.
Science (New York, N.Y.)|August 21, 1992
Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosisJ A Rothnagel, A M Dominey, L D Dempsey, et al.
The British Journal of Dermatology|August 2, 2003
Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutationsS M Morley, M D'Alessandro, C Sexton, et al.
Pageof 15

Showing results (111-120 of 144) with videos related to

Sort By:
Pageof 15
Cell|June 15, 1990
Identification of a major keratinocyte cell envelope protein, loricrinT Mehrel, D Hohl, J A Rothnagel, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 30, 2022
PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndromeG Blanchard, A A Yurchenko, O T Pop, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 6, 2016
Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screeningL Marquardt, M Lacour, M Hoernes, et al.
The British Journal of Dermatology|July 2, 2009
Incidence of bullous pemphigoid and pemphigus in Switzerland: a 2-year prospective studyG Marazza, H C Pham, L Schärer, et al.
The British Journal of Dermatology|March 5, 2014
New and recurrent AAGAB mutations in punctate palmoplantar keratodermaE Pohler, M Huber, S E Boonen, et al.
Current Oncology (Toronto, Ont.)|April 21, 2022
Operationalizing Leadership and Clinician Buy-In to Implement Evidence-Based Tobacco Treatment Programs in Routine Oncology Care: A Mixed-Method Study of the U.S. Cancer Center Cessation InitiativeSarah D Hohl, Jennifer E Bird, Claire V T Nguyen, et al.
Journal of Clinical and Translational Science|January 10, 2025
The intersection of community engagement and team science research: A scoping reviewSarah D Hohl, Erin Abu-Rish Blakeney, Lori Carter-Edwards, et al.
European Journal of Human Genetics : EJHG|July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activityE Petit, M Huber, A Rochat, et al.
Science (New York, N.Y.)|August 21, 1992
Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosisJ A Rothnagel, A M Dominey, L D Dempsey, et al.
The British Journal of Dermatology|August 2, 2003
Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutationsS M Morley, M D'Alessandro, C Sexton, et al.
Pageof 15