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L Pulkkinen

Showing results (51-60 of 138) with videos related to

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The Journal of Infectious Diseases|August 1, 1986
Yersinia enterocolitica plasmid in fecal flora of patients with reactive arthritisA M Viitanen, L Pulkkinen, R Lahesmaa-Rantala, et al.
Arthritis and Rheumatism|March 7, 2001
Widespread pain among 11-year-old Finnish twin pairsM Mikkelsson, J Kaprio, J J Salminen, et al.
Experimental Dermatology|March 13, 2003
Novel member of the mouse desmoglein gene family: Dsg1-betaL Pulkkinen, Y W Choi, A Kljuic, et al.
Human Molecular Genetics|February 1, 1996
Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosaS Kivirikko, J A McGrath, L Pulkkinen, et al.
The Journal of Investigative Dermatology|June 1, 1997
Novel ITGB4 mutations in a patient with junctional epidermolysis bullosa-pyloric atresia syndrome and altered basement membrane zone immunofluorescence for the alpha6beta4 integrinY Takizawa, H Shimizu, T Nishikawa, et al.
Archives of Dermatological Research|June 3, 2000
A de novo glycine substitution mutation in the collagenous domain of COL7A1 in dominant dystrophic epidermolysis bullosaJ Y Lee, C Li, S C Chao, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 4, 1998
Novel compound heterozygous mutations in the plectin gene in epidermolysis bullosa with muscular dystrophy and the use of protein truncation test for detection of premature termination codon mutationsM Dang, L Pulkkinen, F J Smith, et al.
The Journal of Investigative Dermatology|November 5, 1997
Novel glycine substitution mutations in COL7A1 reveal that the Pasini and Cockayne-Touraine variants of dominant dystrophic epidermolysis bullosa are allelicA Kon, K Nomura, L Pulkkinen, et al.
The Journal of Investigative Dermatology|June 1, 1997
A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosa pruriginosaJ Y Lee, L Pulkkinen, H S Liu, et al.
The Journal of Investigative Dermatology|May 1, 1996
Compound heterozygosity for nonsense ans missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosaJ A McGarth, A M Christiano, L Pulkkinen, et al.
Pageof 14

Showing results (51-60 of 138) with videos related to

Sort By:
Pageof 14
The Journal of Infectious Diseases|August 1, 1986
Yersinia enterocolitica plasmid in fecal flora of patients with reactive arthritisA M Viitanen, L Pulkkinen, R Lahesmaa-Rantala, et al.
Arthritis and Rheumatism|March 7, 2001
Widespread pain among 11-year-old Finnish twin pairsM Mikkelsson, J Kaprio, J J Salminen, et al.
Experimental Dermatology|March 13, 2003
Novel member of the mouse desmoglein gene family: Dsg1-betaL Pulkkinen, Y W Choi, A Kljuic, et al.
Human Molecular Genetics|February 1, 1996
Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosaS Kivirikko, J A McGrath, L Pulkkinen, et al.
The Journal of Investigative Dermatology|June 1, 1997
Novel ITGB4 mutations in a patient with junctional epidermolysis bullosa-pyloric atresia syndrome and altered basement membrane zone immunofluorescence for the alpha6beta4 integrinY Takizawa, H Shimizu, T Nishikawa, et al.
Archives of Dermatological Research|June 3, 2000
A de novo glycine substitution mutation in the collagenous domain of COL7A1 in dominant dystrophic epidermolysis bullosaJ Y Lee, C Li, S C Chao, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|March 4, 1998
Novel compound heterozygous mutations in the plectin gene in epidermolysis bullosa with muscular dystrophy and the use of protein truncation test for detection of premature termination codon mutationsM Dang, L Pulkkinen, F J Smith, et al.
The Journal of Investigative Dermatology|November 5, 1997
Novel glycine substitution mutations in COL7A1 reveal that the Pasini and Cockayne-Touraine variants of dominant dystrophic epidermolysis bullosa are allelicA Kon, K Nomura, L Pulkkinen, et al.
The Journal of Investigative Dermatology|June 1, 1997
A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosa pruriginosaJ Y Lee, L Pulkkinen, H S Liu, et al.
The Journal of Investigative Dermatology|May 1, 1996
Compound heterozygosity for nonsense ans missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosaJ A McGarth, A M Christiano, L Pulkkinen, et al.
Pageof 14