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H Schumann

Showing results (61-70 of 90) with videos related to

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Frontiers in Chemistry|April 24, 2015
Changing the topology of protein backbone: the effect of backbone cyclization on the structure and dynamics of a SH3 domainFrank H Schumann, Ranjani Varadan, Praveen P Tayakuniyil, et al.
The Journal of Investigative Dermatology|March 20, 1999
Clustering of COL7A1 mutations in exon 73: implications for mutation analysis in dystrophic epidermolysis bullosaS Mecklenbeck, N Hammami-Hauasli, B Höpfner, et al.
The Journal of Biological Chemistry|July 21, 1998
Some, but not all, glycine substitution mutations in COL7A1 result in intracellular accumulation of collagen VII, loss of anchoring fibrils, and skin blisteringN Hammami-Hauasli, H Schumann, M Raghunath, et al.
Biomolecular NMR Assignments|July 29, 2009
NMR-assignments of a cytosolic domain of the C-terminus of polycystin-2Frank H Schumann, Helen Hoffmeister, Maren Schmidt, et al.
Journal of Molecular and Cellular Cardiology|June 10, 1998
Endotoxin and tumor necrosis factor alpha exert a similar proinflammatory effect in neonatal rat cardiomyocytes, but have different cardiodepressant profilesU Müller-Werdan, H Schumann, H Loppnow, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|November 22, 2021
Esophageal carcinoma in severe recessive dystrophic epidermolysis bullosa-an underestimated complication?A Schwieger-Briel, L Trefzer, H Schumann, et al.
The British Journal of Dermatology|May 30, 2012
Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 geneH Schumann, W Roth, C Has, et al.
The British Journal of Dermatology|February 1, 2011
Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VIIM Leverkus, A Ambach, M Hoefeld-Fegeler, et al.
The Journal of Biological Chemistry|February 1, 2000
Collagen XVII is destabilized by a glycine substitution mutation in the cell adhesion domain Col15K Tasanen, J A Eble, M Aumailley, et al.
The British Journal of Dermatology|September 6, 2019
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort studyA Reimer, M Hess, A Schwieger-Briel, et al.
Pageof 9

Showing results (61-70 of 90) with videos related to

Sort By:
Pageof 9
Frontiers in Chemistry|April 24, 2015
Changing the topology of protein backbone: the effect of backbone cyclization on the structure and dynamics of a SH3 domainFrank H Schumann, Ranjani Varadan, Praveen P Tayakuniyil, et al.
The Journal of Investigative Dermatology|March 20, 1999
Clustering of COL7A1 mutations in exon 73: implications for mutation analysis in dystrophic epidermolysis bullosaS Mecklenbeck, N Hammami-Hauasli, B Höpfner, et al.
The Journal of Biological Chemistry|July 21, 1998
Some, but not all, glycine substitution mutations in COL7A1 result in intracellular accumulation of collagen VII, loss of anchoring fibrils, and skin blisteringN Hammami-Hauasli, H Schumann, M Raghunath, et al.
Biomolecular NMR Assignments|July 29, 2009
NMR-assignments of a cytosolic domain of the C-terminus of polycystin-2Frank H Schumann, Helen Hoffmeister, Maren Schmidt, et al.
Journal of Molecular and Cellular Cardiology|June 10, 1998
Endotoxin and tumor necrosis factor alpha exert a similar proinflammatory effect in neonatal rat cardiomyocytes, but have different cardiodepressant profilesU Müller-Werdan, H Schumann, H Loppnow, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|November 22, 2021
Esophageal carcinoma in severe recessive dystrophic epidermolysis bullosa-an underestimated complication?A Schwieger-Briel, L Trefzer, H Schumann, et al.
The British Journal of Dermatology|May 30, 2012
Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 geneH Schumann, W Roth, C Has, et al.
The British Journal of Dermatology|February 1, 2011
Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VIIM Leverkus, A Ambach, M Hoefeld-Fegeler, et al.
The Journal of Biological Chemistry|February 1, 2000
Collagen XVII is destabilized by a glycine substitution mutation in the cell adhesion domain Col15K Tasanen, J A Eble, M Aumailley, et al.
The British Journal of Dermatology|September 6, 2019
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort studyA Reimer, M Hess, A Schwieger-Briel, et al.
Pageof 9