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L Pulkkinen

Showing results (81-90 of 138) with videos related to

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Genomics|January 1, 1995
Cloning of the beta 3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosaL Pulkkinen, D R Gerecke, A M Christiano, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 6, 1998
Molecular analysis of the human laminin alpha3a chain gene (LAMA3a): a strategy for mutation identification and DNA-based prenatal diagnosis in Herlitz junctional epidermolysis bullosaL Pulkkinen, P B Cserhalmi-Friedman, M Tang, et al.
The Journal of Investigative Dermatology|January 14, 1999
Four novel plectin gene mutations in Japanese patients with epidermolysis bullosa with muscular dystrophy disclosed by heteroduplex scanning and protein truncation testsY Takizawa, H Shimizu, F Rouan, et al.
Antimicrobial Agents and Chemotherapy|August 1, 1985
Emergence of trimethoprim resistance in fecal floraP Huovinen, T Mattila, O Kiminki, et al.
Archives of Dermatological Research|November 7, 1999
Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophyH Shimizu, T Masunaga, Y Kurihara, et al.
The British Journal of Dermatology|December 21, 2000
Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplexD S Morrell, D S Rubenstein, R A Briggaman, et al.
The Journal of Investigative Dermatology|December 18, 1998
Novel premature termination codon mutations in the laminin gamma2-chain gene (LAMC2) in Herlitz junctional epidermolysis bullosaY Takizawa, H Shimizu, L Pulkkinen, et al.
The Journal of Investigative Dermatology|April 1, 1995
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosaJ A McGrath, L Pulkkinen, A M Christiano, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31B Udd, H Haravuori, H Kalimo, et al.
The Journal of Investigative Dermatology|February 17, 2001
Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C geneA Nakano, K Nomura, H Nakano, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
Genomics|January 1, 1995
Cloning of the beta 3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosaL Pulkkinen, D R Gerecke, A M Christiano, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 6, 1998
Molecular analysis of the human laminin alpha3a chain gene (LAMA3a): a strategy for mutation identification and DNA-based prenatal diagnosis in Herlitz junctional epidermolysis bullosaL Pulkkinen, P B Cserhalmi-Friedman, M Tang, et al.
The Journal of Investigative Dermatology|January 14, 1999
Four novel plectin gene mutations in Japanese patients with epidermolysis bullosa with muscular dystrophy disclosed by heteroduplex scanning and protein truncation testsY Takizawa, H Shimizu, F Rouan, et al.
Antimicrobial Agents and Chemotherapy|August 1, 1985
Emergence of trimethoprim resistance in fecal floraP Huovinen, T Mattila, O Kiminki, et al.
Archives of Dermatological Research|November 7, 1999
Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophyH Shimizu, T Masunaga, Y Kurihara, et al.
The British Journal of Dermatology|December 21, 2000
Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplexD S Morrell, D S Rubenstein, R A Briggaman, et al.
The Journal of Investigative Dermatology|December 18, 1998
Novel premature termination codon mutations in the laminin gamma2-chain gene (LAMC2) in Herlitz junctional epidermolysis bullosaY Takizawa, H Shimizu, L Pulkkinen, et al.
The Journal of Investigative Dermatology|April 1, 1995
Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosaJ A McGrath, L Pulkkinen, A M Christiano, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31B Udd, H Haravuori, H Kalimo, et al.
The Journal of Investigative Dermatology|February 17, 2001
Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C geneA Nakano, K Nomura, H Nakano, et al.
Pageof 14