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The Journal of Investigative Dermatology
|
September 18, 1998
Role of Staphylococcus aureus surface-associated proteins in the attachment to cultured HaCaT keratinocytes in a new adhesion assay
M Mempel, T Schmidt, S Weidinger, et al.
American Journal of Human Genetics
|
April 1, 1990
Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern
M D Holmes, M L Brantly, D T Curiel, et al.
The British Journal of Dermatology
|
July 10, 2013
A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrin
L Cifuentes, D Kiritsi, W Chen, et al.
Human Reproduction (Oxford, England)
|
December 4, 2003
Mast cell-sperm interaction: evidence for tryptase and proteinase-activated receptors in the regulation of sperm motility
S Weidinger, A Mayerhofer, M B Frungieri, et al.
Allergy
|
September 8, 2011
Itches and scratches – is there a link between eczema, ADHD, sleep disruption and food hypersensitivity?
M Romanos, A Buske-Kirschbaum, R Fölster-Holst, et al.
The British Journal of Dermatology
|
October 26, 2021
Tralokinumab plus topical corticosteroids in adults with severe atopic dermatitis and inadequate response to or intolerance of ciclosporin A: a placebo-controlled, randomized, phase III clinical trial (ECZTRA 7)
J Gutermuth, A E Pink, M Worm, et al.
Human Genetics
|
January 1, 1983
Isoelectric focusing with immobilized pH gradients for the analysis of transferrin (Tf) subtypes and variants
A Görg, J Weser, R Westermeier, et al.
American Journal of Human Genetics
|
December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele
J P Faber, W Poller, S Weidinger, et al.
Lancet (London, England)
|
June 20, 1992
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease
W Poller, J P Faber, S Scholz, et al.
Human Genetics
|
August 1, 1990
Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant
A Graham, K Hayes, S Weidinger, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 129) with videos related to
Sort By:
Page
of 13
The Journal of Investigative Dermatology
|
September 18, 1998
Role of Staphylococcus aureus surface-associated proteins in the attachment to cultured HaCaT keratinocytes in a new adhesion assay
M Mempel, T Schmidt, S Weidinger, et al.
American Journal of Human Genetics
|
April 1, 1990
Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern
M D Holmes, M L Brantly, D T Curiel, et al.
The British Journal of Dermatology
|
July 10, 2013
A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrin
L Cifuentes, D Kiritsi, W Chen, et al.
Human Reproduction (Oxford, England)
|
December 4, 2003
Mast cell-sperm interaction: evidence for tryptase and proteinase-activated receptors in the regulation of sperm motility
S Weidinger, A Mayerhofer, M B Frungieri, et al.
Allergy
|
September 8, 2011
Itches and scratches – is there a link between eczema, ADHD, sleep disruption and food hypersensitivity?
M Romanos, A Buske-Kirschbaum, R Fölster-Holst, et al.
The British Journal of Dermatology
|
October 26, 2021
Tralokinumab plus topical corticosteroids in adults with severe atopic dermatitis and inadequate response to or intolerance of ciclosporin A: a placebo-controlled, randomized, phase III clinical trial (ECZTRA 7)
J Gutermuth, A E Pink, M Worm, et al.
Human Genetics
|
January 1, 1983
Isoelectric focusing with immobilized pH gradients for the analysis of transferrin (Tf) subtypes and variants
A Görg, J Weser, R Westermeier, et al.
American Journal of Human Genetics
|
December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele
J P Faber, W Poller, S Weidinger, et al.
Lancet (London, England)
|
June 20, 1992
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease
W Poller, J P Faber, S Scholz, et al.
Human Genetics
|
August 1, 1990
Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant
A Graham, K Hayes, S Weidinger, et al.
Page
of 13