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J W Bauer

Showing results (21-30 of 64) with videos related to

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The Journal of Clinical Investigation|May 20, 1999
Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutationT N Darling, C Yee, J W Bauer, et al.
Journal of Dairy Science|January 22, 2026
Association of calving factors and labor duration with postpartum uterine health in Holstein cattleJ W Bauer, T A Burnett, A M L Madureira, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 31, 1999
[Prenatal diagnosis of recessive hereditary dystrophic epidermolysis bullosa with haplotype analysis of the type VII collagen gene]J W Bauer, S Ortiz, M Hengstschläger, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 25, 2017
Vismodegib for recurrent locally destructive basal cell carcinoma in a renal transplant patientP Koelblinger, R Dummer, M Laimer, et al.
Bone Marrow Transplantation|February 14, 2012
Successful allogeneic cord blood transplantation in a patient with Evans syndrome leads to correction of hereditary angioedema type I as secondary effectA Klausegger, M Wiednig, C Urban, et al.
Acta Dermato-Venereologica|September 18, 2001
Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosaF Weber, J W Bauer, N Sepp, et al.
Journal of Neuroendocrinology|May 11, 2011
Sex-Related Differences in Chromogranin A, Chromogranin B and Secretogranin II Gene Expression in Rat PituitaryR Fischer-Colbrie, K W Schmid, S K Mahata, et al.
Gene Therapy|July 20, 2016
Construction and validation of an RNA trans-splicing molecule suitable to repair a large number of COL7A1 mutationsB Tockner, T Kocher, S Hainzl, et al.
The British Journal of Dermatology|July 21, 2005
Epidermolysis bullosa naevi reveal a distinctive dermoscopic patternC M Lanschuetzer, M Emberger, M Laimer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 19, 2022
Phenotypic alleviation in LAMB3-mutated severe junctional epidermolysis bullosaK Medek, A Klausegger, K Ude-Schoder, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|May 20, 1999
Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutationT N Darling, C Yee, J W Bauer, et al.
Journal of Dairy Science|January 22, 2026
Association of calving factors and labor duration with postpartum uterine health in Holstein cattleJ W Bauer, T A Burnett, A M L Madureira, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 31, 1999
[Prenatal diagnosis of recessive hereditary dystrophic epidermolysis bullosa with haplotype analysis of the type VII collagen gene]J W Bauer, S Ortiz, M Hengstschläger, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 25, 2017
Vismodegib for recurrent locally destructive basal cell carcinoma in a renal transplant patientP Koelblinger, R Dummer, M Laimer, et al.
Bone Marrow Transplantation|February 14, 2012
Successful allogeneic cord blood transplantation in a patient with Evans syndrome leads to correction of hereditary angioedema type I as secondary effectA Klausegger, M Wiednig, C Urban, et al.
Acta Dermato-Venereologica|September 18, 2001
Squamous cell carcinoma in junctional and dystrophic epidermolysis bullosaF Weber, J W Bauer, N Sepp, et al.
Journal of Neuroendocrinology|May 11, 2011
Sex-Related Differences in Chromogranin A, Chromogranin B and Secretogranin II Gene Expression in Rat PituitaryR Fischer-Colbrie, K W Schmid, S K Mahata, et al.
Gene Therapy|July 20, 2016
Construction and validation of an RNA trans-splicing molecule suitable to repair a large number of COL7A1 mutationsB Tockner, T Kocher, S Hainzl, et al.
The British Journal of Dermatology|July 21, 2005
Epidermolysis bullosa naevi reveal a distinctive dermoscopic patternC M Lanschuetzer, M Emberger, M Laimer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 19, 2022
Phenotypic alleviation in LAMB3-mutated severe junctional epidermolysis bullosaK Medek, A Klausegger, K Ude-Schoder, et al.
Pageof 7