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Genomics|November 20, 1995
Cloning of the laminin alpha 3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosaF Vidal, C Baudoin, C Miquel, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 1, 1993
Basement membrane proteins kalinin and nicein are structurally and immunologically identicalM P Marinkovich, P Verrando, D R Keene, et al.
The Journal of Investigative Dermatology|August 1, 1997
Predominance of the recurrent mutation R635X in the LAMB3 gene in European patients with Herlitz junctional epidermolysis bullosa has implications for mutation detection strategyL Pulkkinen, G Meneguzzi, J A McGrath, et al.
The Journal of Investigative Dermatology|February 13, 2001
A homozygous nonsense mutation in type XVII collagen gene (COL17A1) uncovers an alternatively spliced mRNA accounting for an unusually mild form of non-Herlitz junctional epidermolysis bullosaL Ruzzi, H Pas, P Posteraro, et al.
Intervirology|January 1, 1981
Lack of association between BK virus and ependymomas, malignant tumors of pancreatic islets, osteosarcomas and other human tumorsM P Grossi, G Meneguzzi, N Chenciner, et al.
The Journal of General Virology|December 1, 1982
Transformation of human embryonic fibroblasts by BK virus, BK virus DNA and a subgenomic BK virus DNA fragmentM P Grossi, A Caputo, G Meneguzzi, et al.
Oncogene|April 4, 2007
Id3 is a novel regulator of p27kip1 mRNA in early G1 phase and is required for cell-cycle progressionA-A Chassot, L Turchi, T Virolle, et al.
International Journal of Systematic and Evolutionary Microbiology|April 25, 2015
Detection and identification of a novel 16SrXIII subgroup phytoplasma associated with strawberry red leaf disease in ArgentinaFranco D Fernández, Natalia G Meneguzzi, Fabiana A Guzmán, et al.
Gene Therapy|February 4, 1999
Corrective gene transfer of keratinocytes from patients with junctional epidermolysis bullosa restores assembly of hemidesmosomes in reconstructed epitheliaJ Vailly, L Gagnoux-Palacios, E Dell'Ambra, et al.
The Journal of Investigative Dermatology|April 1, 1995
Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrenceJ Vailly, L Pulkkinen, C Miquel, et al.
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