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Holm Schneider

Showing results (1-10 of 106) with videos related to

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Deutsches Arzteblatt International|April 29, 2014
Consider further differential diagnosesHolm Schneider
Frontiers in Genetics|September 23, 2022
Ectodermal dysplasias: New perspectives on the treatment of so far immedicable genetic disordersHolm Schneider
Zeitschrift Fur Geburtshilfe Und Neonatologie|July 22, 2024
Holm Schneider
Human Genetics|October 21, 2010
Gene symbol: LAMC2. Disease: Epidermolysis Bullosa, HerlitzHolm Schneider, Christiane Muehle
European Journal of Dermatology : EJD|March 7, 2009
X-chromosomal insertions at a recurrent site causing ectodermal dysplasiaHolm Schneider, Christiane Mühle
Clinical Genetics|January 10, 2019
Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasiaSigrun Wohlfart, Holm Schneider
Methods in Molecular Biology (Clifton, N.J.)|May 19, 2011
In vivo evaluation of gene transfer into mesenchymal cells (in view of cartilage repair)Kolja Gelse, Holm Schneider
Frontiers in Genetics|November 4, 2021
Editorial: Gene, Cell and Protein Replacement Therapy for Genetic Muscle, Bone and Skin DisordersHolm Schneider, Michele De Luca
European Journal of Cell Biology|September 27, 2006
Biological function of laminin-5 and pathogenic impact of its deficiencyHolm Schneider, Christiane Mühle, Frederic Pacho
Journal of Human Genetics|June 17, 2016
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangementsSigrun Wohlfart, Johanna Hammersen, Holm Schneider
Pageof 11

Showing results (1-10 of 106) with videos related to

Sort By:
Pageof 11
Deutsches Arzteblatt International|April 29, 2014
Consider further differential diagnosesHolm Schneider
Frontiers in Genetics|September 23, 2022
Ectodermal dysplasias: New perspectives on the treatment of so far immedicable genetic disordersHolm Schneider
Zeitschrift Fur Geburtshilfe Und Neonatologie|July 22, 2024
Holm Schneider
Human Genetics|October 21, 2010
Gene symbol: LAMC2. Disease: Epidermolysis Bullosa, HerlitzHolm Schneider, Christiane Muehle
European Journal of Dermatology : EJD|March 7, 2009
X-chromosomal insertions at a recurrent site causing ectodermal dysplasiaHolm Schneider, Christiane Mühle
Clinical Genetics|January 10, 2019
Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasiaSigrun Wohlfart, Holm Schneider
Methods in Molecular Biology (Clifton, N.J.)|May 19, 2011
In vivo evaluation of gene transfer into mesenchymal cells (in view of cartilage repair)Kolja Gelse, Holm Schneider
Frontiers in Genetics|November 4, 2021
Editorial: Gene, Cell and Protein Replacement Therapy for Genetic Muscle, Bone and Skin DisordersHolm Schneider, Michele De Luca
European Journal of Cell Biology|September 27, 2006
Biological function of laminin-5 and pathogenic impact of its deficiencyHolm Schneider, Christiane Mühle, Frederic Pacho
Journal of Human Genetics|June 17, 2016
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangementsSigrun Wohlfart, Johanna Hammersen, Holm Schneider
Pageof 11