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S Weidinger

Showing results (71-80 of 129) with videos related to

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European Journal of Pediatrics|March 1, 1997
Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG)K Heyne, H Henry, B Messerli, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1993
Genetic polymorphism in the Garfagnana population (Tuscany)G Paoli, S Tofanelli, M G Franceschi, et al.
Human Genetics|March 1, 1988
A "new" allele of esterase D in a retinoblastoma familyF Munier, G Pescia, A Balmer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 10, 2012
GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruptionM Zirbs, C Pürner, J T M Buters, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 19, 2002
Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiencyH K Harms, K P Zimmer, K Kurnik, et al.
Human Mutation|January 29, 2000
Identification and molecular characterization of the new alpha-1-antitrypsin deficient allele PI Y barcelona (Asp256-->Val and Pro391-->His). Mutations in brief no. 174. OnlineR Jardi, F Rodriguez, M Miravitlles, et al.
Human Heredity|January 1, 1991
New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity caseK Bender, D Kasulke, A Mayerovà, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|March 16, 2007
Monocyte-derived dendritic cells from highly atopic individuals are not impaired in their pro-inflammatory response to toll-like receptor ligandsD Terhorst, B N Kalali, S Weidinger, et al.
The Journal of Allergy and Clinical Immunology|July 31, 2004
Association between atopy and cryptorchidismS Weidinger, T Schäfer, B Malek, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Molecular characterisation of the defective alpha 1-antitrypsin alleles PI Mwurzburg (Pro369Ser), Mheerlen (Pro369Leu), and Q0lisbon (Thr68Ile)W Poller, F Merklein, S Schneider-Rasp, et al.
Pageof 13

Showing results (71-80 of 129) with videos related to

Sort By:
Pageof 13
European Journal of Pediatrics|March 1, 1997
Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG)K Heyne, H Henry, B Messerli, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1993
Genetic polymorphism in the Garfagnana population (Tuscany)G Paoli, S Tofanelli, M G Franceschi, et al.
Human Genetics|March 1, 1988
A "new" allele of esterase D in a retinoblastoma familyF Munier, G Pescia, A Balmer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 10, 2012
GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruptionM Zirbs, C Pürner, J T M Buters, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 19, 2002
Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiencyH K Harms, K P Zimmer, K Kurnik, et al.
Human Mutation|January 29, 2000
Identification and molecular characterization of the new alpha-1-antitrypsin deficient allele PI Y barcelona (Asp256-->Val and Pro391-->His). Mutations in brief no. 174. OnlineR Jardi, F Rodriguez, M Miravitlles, et al.
Human Heredity|January 1, 1991
New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity caseK Bender, D Kasulke, A Mayerovà, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|March 16, 2007
Monocyte-derived dendritic cells from highly atopic individuals are not impaired in their pro-inflammatory response to toll-like receptor ligandsD Terhorst, B N Kalali, S Weidinger, et al.
The Journal of Allergy and Clinical Immunology|July 31, 2004
Association between atopy and cryptorchidismS Weidinger, T Schäfer, B Malek, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Molecular characterisation of the defective alpha 1-antitrypsin alleles PI Mwurzburg (Pro369Ser), Mheerlen (Pro369Leu), and Q0lisbon (Thr68Ile)W Poller, F Merklein, S Schneider-Rasp, et al.
Pageof 13