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J L Jorcano

Showing results (71-80 of 74) with videos related to

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Histology and Histopathology|July 29, 2006
Skin gene therapy for acquired and inherited disordersM Carretero, M J Escámez, F Prada, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 28, 2001
A cutaneous gene therapy approach to human leptin deficiencies: correction of the murine ob/ob phenotype using leptin-targeted keratinocyte graftsF Larcher, M Del Rio, F Serrano, et al.
Oncogene|October 26, 2005
Hair cycle and wound healing in mice with a keratinocyte-restricted deletion of FAKS Essayem, B Kovacic-Milivojevic, C Baumbusch, et al.
The British Journal of Dermatology|February 27, 2010
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutationM J Escámez, M García, N Cuadrado-Corrales, et al.
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Showing results (71-80 of 74) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 74 results.
Histology and Histopathology|July 29, 2006
Skin gene therapy for acquired and inherited disordersM Carretero, M J Escámez, F Prada, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 28, 2001
A cutaneous gene therapy approach to human leptin deficiencies: correction of the murine ob/ob phenotype using leptin-targeted keratinocyte graftsF Larcher, M Del Rio, F Serrano, et al.
Oncogene|October 26, 2005
Hair cycle and wound healing in mice with a keratinocyte-restricted deletion of FAKS Essayem, B Kovacic-Milivojevic, C Baumbusch, et al.
The British Journal of Dermatology|February 27, 2010
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutationM J Escámez, M García, N Cuadrado-Corrales, et al.
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