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S Weidinger

Showing results (81-90 of 129) with videos related to

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Allergy|April 15, 2011
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activitiesL Maintz, C-F Yu, E Rodríguez, et al.
Vox Sanguinis|January 1, 1993
Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclatureI Yuasa, S Weidinger, K Umetsu, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 20, 2021
[Quality of care for patients with atopic dermatitis in Germany-no improvements in indicators after ten years]A Langenbruch, N Mohr, F Abeck, et al.
The British Journal of Dermatology|February 1, 2006
The course of eczema in children aged 5-7 years and its relation to atopy: differences between boys and girlsM Möhrenschlager, T Schäfer, J Huss-Marp, et al.
The Clinical Investigator|July 1, 1994
High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failureM Pecherstorfer, I Zimmer-Roth, S Weidinger, et al.
Human Reproduction (Oxford, England)|December 4, 2004
Tryptase inhibits motility of human spermatozoa mainly by activation of the mitogen-activated protein kinase pathwayS Weidinger, A Mayerhofer, L Kunz, et al.
Allergy|April 19, 2016
Childhood atopic dermatitis-Brain-derived neurotrophic factor correlates with serum eosinophil cationic protein and disease severityR Fölster-Holst, E Papakonstantinou, U Rüdrich, et al.
The British Journal of Dermatology|June 20, 2002
Invasion of human keratinocytes by Staphylococcus aureus and intracellular bacterial persistence represent haemolysin-independent virulence mechanisms that are followed by features of necrotic and apoptotic keratinocyte cell deathM Mempel, C Schnopp, M Hojka, et al.
Genomics|September 1, 1993
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung diseaseW Poller, J P Faber, S Weidinger, et al.
The British Journal of Dermatology|October 9, 2012
Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitisM J Visser, L Landeck, L E Campbell, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Allergy|April 15, 2011
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activitiesL Maintz, C-F Yu, E Rodríguez, et al.
Vox Sanguinis|January 1, 1993
Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclatureI Yuasa, S Weidinger, K Umetsu, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 20, 2021
[Quality of care for patients with atopic dermatitis in Germany-no improvements in indicators after ten years]A Langenbruch, N Mohr, F Abeck, et al.
The British Journal of Dermatology|February 1, 2006
The course of eczema in children aged 5-7 years and its relation to atopy: differences between boys and girlsM Möhrenschlager, T Schäfer, J Huss-Marp, et al.
The Clinical Investigator|July 1, 1994
High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failureM Pecherstorfer, I Zimmer-Roth, S Weidinger, et al.
Human Reproduction (Oxford, England)|December 4, 2004
Tryptase inhibits motility of human spermatozoa mainly by activation of the mitogen-activated protein kinase pathwayS Weidinger, A Mayerhofer, L Kunz, et al.
Allergy|April 19, 2016
Childhood atopic dermatitis-Brain-derived neurotrophic factor correlates with serum eosinophil cationic protein and disease severityR Fölster-Holst, E Papakonstantinou, U Rüdrich, et al.
The British Journal of Dermatology|June 20, 2002
Invasion of human keratinocytes by Staphylococcus aureus and intracellular bacterial persistence represent haemolysin-independent virulence mechanisms that are followed by features of necrotic and apoptotic keratinocyte cell deathM Mempel, C Schnopp, M Hojka, et al.
Genomics|September 1, 1993
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung diseaseW Poller, J P Faber, S Weidinger, et al.
The British Journal of Dermatology|October 9, 2012
Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitisM J Visser, L Landeck, L E Campbell, et al.
Pageof 13