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A Klausegger

Showing results (11-20 of 19) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2006
Introducing a fast and simple PCR-RFLP analysis for the detection of mutant thiopurine S-methyltransferase alleles TPMT*3A and TPMT*3CK Oender, C M Lanschuetzer, M Laimer, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|May 12, 2009
[Hereditary blistering diseases. Symptoms, diagnosis and treatment of epidermolysis bullosa]M Laimer, C M Lanschützer, E Nischler, et al.
Experimental Dermatology|March 13, 2003
Development of spliceosome-mediated RNA trans-splicing (SMaRT) for the correction of inherited skin diseasesG Dallinger, M Puttaraju, L G Mitchell, et al.
Human Genetics|August 11, 2004
Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, KoebnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Journal of Cutaneous Pathology|September 26, 2003
Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorderC M Lanschuetzer, W H Muss, M Emberger, et al.
Clinical and Experimental Dermatology|February 1, 2003
A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type KöbnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
The British Journal of Dermatology|August 3, 2016
Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significanceI Fuentes, M Campos, G Repetto, et al.
The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.
The British Journal of Dermatology|January 13, 2006
Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosaM Laimer, J W Bauer, A Klausegger, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2006
Introducing a fast and simple PCR-RFLP analysis for the detection of mutant thiopurine S-methyltransferase alleles TPMT*3A and TPMT*3CK Oender, C M Lanschuetzer, M Laimer, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|May 12, 2009
[Hereditary blistering diseases. Symptoms, diagnosis and treatment of epidermolysis bullosa]M Laimer, C M Lanschützer, E Nischler, et al.
Experimental Dermatology|March 13, 2003
Development of spliceosome-mediated RNA trans-splicing (SMaRT) for the correction of inherited skin diseasesG Dallinger, M Puttaraju, L G Mitchell, et al.
Human Genetics|August 11, 2004
Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, KoebnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Journal of Cutaneous Pathology|September 26, 2003
Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorderC M Lanschuetzer, W H Muss, M Emberger, et al.
Clinical and Experimental Dermatology|February 1, 2003
A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type KöbnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
The British Journal of Dermatology|August 3, 2016
Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significanceI Fuentes, M Campos, G Repetto, et al.
The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.
The British Journal of Dermatology|January 13, 2006
Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosaM Laimer, J W Bauer, A Klausegger, et al.
Pageof 2