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L Pulkkinen

Showing results (61-70 of 138) with videos related to

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Nature Genetics|March 1, 1994
Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosaL Pulkkinen, A M Christiano, T Airenne, et al.
Alcoholism, Clinical and Experimental Research|November 15, 2001
Drinking or abstaining at age 14? A genetic epidemiological studyR J Rose, D M Dick, R J Viken, et al.
Terapevticheskii Arkhiv|January 1, 1986
[Do bacterial antigens persist in patients with reactive arthritis?]A Toivanen, A M Viitanen, T H Stälberg, et al.
Human Mutation|February 5, 2000
Laminin 5 genes and Herlitz junctional epidermolysis bullosa: novel mutations and polymorphisms in the LAMB3 and LAMC2 genes. Mutations in brief no. 190. OnlineA Kon, L Pulkkinen, M Hara, et al.
The Journal of Investigative Dermatology|May 14, 1998
Maternal uniparental meroisodisomy in the LAMB3 region of chromosome 1 results in lethal junctional epidermolysis bullosaY Takizawa, L Pulkkinen, H Shimizu, et al.
The Journal of Investigative Dermatology|December 18, 1998
Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitz junctional epidermolysis bullosa, and their application for prenatal testingY Takizawa, H Shimizu, L Pulkkinen, et al.
The Journal of Investigative Dermatology|May 8, 1999
Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1)M F Jonkman, G Moreno, F Rouan, et al.
American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 31, 1999
[Prenatal diagnosis of recessive hereditary dystrophic epidermolysis bullosa with haplotype analysis of the type VII collagen gene]J W Bauer, S Ortiz, M Hengstschläger, et al.
The Journal of Investigative Dermatology|January 15, 2000
Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosaL Pulkkinen, M P Marinkovich, H T Tran, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
Nature Genetics|March 1, 1994
Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosaL Pulkkinen, A M Christiano, T Airenne, et al.
Alcoholism, Clinical and Experimental Research|November 15, 2001
Drinking or abstaining at age 14? A genetic epidemiological studyR J Rose, D M Dick, R J Viken, et al.
Terapevticheskii Arkhiv|January 1, 1986
[Do bacterial antigens persist in patients with reactive arthritis?]A Toivanen, A M Viitanen, T H Stälberg, et al.
Human Mutation|February 5, 2000
Laminin 5 genes and Herlitz junctional epidermolysis bullosa: novel mutations and polymorphisms in the LAMB3 and LAMC2 genes. Mutations in brief no. 190. OnlineA Kon, L Pulkkinen, M Hara, et al.
The Journal of Investigative Dermatology|May 14, 1998
Maternal uniparental meroisodisomy in the LAMB3 region of chromosome 1 results in lethal junctional epidermolysis bullosaY Takizawa, L Pulkkinen, H Shimizu, et al.
The Journal of Investigative Dermatology|December 18, 1998
Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitz junctional epidermolysis bullosa, and their application for prenatal testingY Takizawa, H Shimizu, L Pulkkinen, et al.
The Journal of Investigative Dermatology|May 8, 1999
Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1)M F Jonkman, G Moreno, F Rouan, et al.
American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 31, 1999
[Prenatal diagnosis of recessive hereditary dystrophic epidermolysis bullosa with haplotype analysis of the type VII collagen gene]J W Bauer, S Ortiz, M Hengstschläger, et al.
The Journal of Investigative Dermatology|January 15, 2000
Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosaL Pulkkinen, M P Marinkovich, H T Tran, et al.
Pageof 14