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E Dondi

Showing results (1-10 of 20) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 26, 2000
A dual role for the kinase-like domain of the tyrosine kinase Tyk2 in interferon-alpha signalingT C Yeh, E Dondi, G Uze, et al.
Journal of Neuroimmunology|May 1, 1994
Association of Km3 allotype with increased serum levels of autoantibodies against muscle acetylcholine receptor in myasthenia gravisE Dondi, P Gajdos, J F Bach, et al.
Journal of the Neurological Sciences|September 28, 2001
Polymorphic markers in MHC class II/III region: a study on Italian patients with myasthenia gravisD Franciotta, M Cuccia, E Dondi, et al.
Dermatology (Basel, Switzerland)|January 1, 1992
Polymorphisms of HLA class III genes in allergic contact dermatitisG Orecchia, L Perfetti, O Finco, et al.
Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|March 31, 2000
Lymphocyte expression of human leukocyte antigen class II molecules in patients with chronic obstructive pulmonary diseaseH Recalde, M Cuccia, T Oggionni, et al.
The Journal of Biological Chemistry|June 16, 2001
The receptor interaction region of Tyk2 contains a motif required for its nuclear localizationJ Ragimbeau, E Dondi, A Vasserot, et al.
Complement and Inflammation|January 1, 1991
Sarcoidosis and major histocompatibility complex genes with special emphasis on BF F subtypesO Finco, M Martinetti, E Dondi, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|October 1, 1994
Molecular analysis of CYP21 gene mutations carried on HLA-B14 positive haplotypesE Dondi, M Cuccia, E Keller, et al.
Clinical Endocrinology|January 1, 1994
Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their familiesD Larizza, M Cuccia, M Martinetti, et al.
Clinical Endocrinology|July 17, 1998
Exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation and evidence for CYP21B gene point mutations in true precocious pubertyM Cisternino, E Dondi, M Martinetti, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Proceedings of the National Academy of Sciences of the United States of America|July 26, 2000
A dual role for the kinase-like domain of the tyrosine kinase Tyk2 in interferon-alpha signalingT C Yeh, E Dondi, G Uze, et al.
Journal of Neuroimmunology|May 1, 1994
Association of Km3 allotype with increased serum levels of autoantibodies against muscle acetylcholine receptor in myasthenia gravisE Dondi, P Gajdos, J F Bach, et al.
Journal of the Neurological Sciences|September 28, 2001
Polymorphic markers in MHC class II/III region: a study on Italian patients with myasthenia gravisD Franciotta, M Cuccia, E Dondi, et al.
Dermatology (Basel, Switzerland)|January 1, 1992
Polymorphisms of HLA class III genes in allergic contact dermatitisG Orecchia, L Perfetti, O Finco, et al.
Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|March 31, 2000
Lymphocyte expression of human leukocyte antigen class II molecules in patients with chronic obstructive pulmonary diseaseH Recalde, M Cuccia, T Oggionni, et al.
The Journal of Biological Chemistry|June 16, 2001
The receptor interaction region of Tyk2 contains a motif required for its nuclear localizationJ Ragimbeau, E Dondi, A Vasserot, et al.
Complement and Inflammation|January 1, 1991
Sarcoidosis and major histocompatibility complex genes with special emphasis on BF F subtypesO Finco, M Martinetti, E Dondi, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|October 1, 1994
Molecular analysis of CYP21 gene mutations carried on HLA-B14 positive haplotypesE Dondi, M Cuccia, E Keller, et al.
Clinical Endocrinology|January 1, 1994
Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their familiesD Larizza, M Cuccia, M Martinetti, et al.
Clinical Endocrinology|July 17, 1998
Exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation and evidence for CYP21B gene point mutations in true precocious pubertyM Cisternino, E Dondi, M Martinetti, et al.
Pageof 2