Search research articles
Contact Us
Filters
Showing results (1-10 of 20) with videos related to
Page
of 2
Sort By:
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 signaling
T 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 gravis
E 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 gravis
D Franciotta, M Cuccia, E Dondi, et al.
Dermatology (Basel, Switzerland)
|
January 1, 1992
Polymorphisms of HLA class III genes in allergic contact dermatitis
G 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 disease
H 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 localization
J 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 subtypes
O 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 haplotypes
E 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 families
D 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 puberty
M Cisternino, E Dondi, M Martinetti, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 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 signaling
T 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 gravis
E 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 gravis
D Franciotta, M Cuccia, E Dondi, et al.
Dermatology (Basel, Switzerland)
|
January 1, 1992
Polymorphisms of HLA class III genes in allergic contact dermatitis
G 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 disease
H 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 localization
J 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 subtypes
O 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 haplotypes
E 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 families
D 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 puberty
M Cisternino, E Dondi, M Martinetti, et al.
Page
of 2