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Journal of Neuroimmunology
|
November 26, 2002
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis
M Gomez-Lira, G Moretto, D Bonamini, et al.
Journal of Medical Genetics
|
December 1, 1994
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation
M Gomez-Lira, A Sangalli, P F Pignatti, et al.
Gene
|
December 10, 2020
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure
S Fochi, E Orlandi, L Ceccuzzi, et al.
Human Genetics
|
July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene
M Mottes, A Sangalli, M Valli, et al.
Human Mutation
|
July 20, 2001
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis
C Castellani, M Gomez Lira, L Frulloni, et al.
Human Mutation
|
January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta
M Mottes, M M Gomez Lira, M Valli, et al.
International Journal of Immunogenetics
|
March 22, 2007
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk
S Mazzola, M Gomez Lira, M D Benedetti, et al.
The Journal of Biological Chemistry
|
January 25, 1991
A de novo G to T transversion in a pro-alpha 1 (I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain
M Valli, M Mottes, R Tenni, et al.
Molecular Biology Reports
|
November 14, 2018
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood
S Ferronato, A Scuro, S Fochi, et al.
Neurology
|
November 4, 2000
Adult-onset MLD: a gene mutation with isolated polyneuropathy
K J Felice, M Gomez Lira, M Natowicz, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Journal of Neuroimmunology
|
November 26, 2002
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis
M Gomez-Lira, G Moretto, D Bonamini, et al.
Journal of Medical Genetics
|
December 1, 1994
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation
M Gomez-Lira, A Sangalli, P F Pignatti, et al.
Gene
|
December 10, 2020
Identification of suitable mRNAs and microRNAs as reference genes for expression analyses in skin cells under sex hormone exposure
S Fochi, E Orlandi, L Ceccuzzi, et al.
Human Genetics
|
July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene
M Mottes, A Sangalli, M Valli, et al.
Human Mutation
|
July 20, 2001
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis
C Castellani, M Gomez Lira, L Frulloni, et al.
Human Mutation
|
January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta
M Mottes, M M Gomez Lira, M Valli, et al.
International Journal of Immunogenetics
|
March 22, 2007
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk
S Mazzola, M Gomez Lira, M D Benedetti, et al.
The Journal of Biological Chemistry
|
January 25, 1991
A de novo G to T transversion in a pro-alpha 1 (I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain
M Valli, M Mottes, R Tenni, et al.
Molecular Biology Reports
|
November 14, 2018
Expression of TLR4-PTGE2 signaling genes in atherosclerotic carotid plaques and peripheral blood
S Ferronato, A Scuro, S Fochi, et al.
Neurology
|
November 4, 2000
Adult-onset MLD: a gene mutation with isolated polyneuropathy
K J Felice, M Gomez Lira, M Natowicz, et al.
Page
of 3