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Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1989
A monoclonal anti-double-stranded DNA autoantibody binds to a 94-kDa cell-surface protein on various cell types via nucleosomes or a DNA-histone complex
L Jacob, J P Viard, B Allenet, et al.
Allergy
|
July 22, 2014
Casein-specific IL-4- and IL-13-secreting T cells: a tool to implement diagnosis of cow's milk allergy
B Michaud, J Aroulandom, N Baiz, et al.
Nature Genetics
|
October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
S Laberge-le Couteulx, H H Jung, P Labauge, et al.
Human Genetics
|
November 1, 1996
Age-dependent penetrance and mapping of the locus for juvenile and early-onset open-angle glaucoma on chromosome 1q (GLC1A) in a French family
A Meyer, A Béchetoille, F Valtot, et al.
Journal of Medical Genetics
|
July 1, 1997
Genetic heterogeneity of primary open angle glaucoma and ocular hypertension: linkage to GLC1A associated with an increased risk of severe glaucomatous optic neuropathy
A P Brézin, A Béchetoille, P Hamard, et al.
European Journal of Immunology
|
February 10, 2004
Exacerbated Th2-mediated airway inflammation and hyperresponsiveness in autoimmune diabetes-prone NOD mice: a critical role for CD1d-dependent NKT cells
Luiza M Araujo, Jean Lefort, Marie-Anne Nahori, et al.
Klinische Wochenschrift
|
January 15, 1988
Cyclosporin-associated nephropathy in patients with autoimmune diseases
M J Mihatsch, J F Bach, H M Coovadia, et al.
Lancet (London, England)
|
December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
A Joutel, K Vahedi, C Corpechot, et al.
Journal of Autoimmunity
|
March 14, 1998
Treatment of recalcitrant plaque psoriasis with a humanized non-depleting antibody to CD4
H Bachelez, B Flageul, L Dubertret, et al.
Human Molecular Genetics
|
November 5, 1997
Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucoma
M F Adam, A Belmouden, P Binisti, et al.
Page
of 48
Search research articles
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Showing results (461-470 of 478) with videos related to
Sort By:
Page
of 48
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1989
A monoclonal anti-double-stranded DNA autoantibody binds to a 94-kDa cell-surface protein on various cell types via nucleosomes or a DNA-histone complex
L Jacob, J P Viard, B Allenet, et al.
Allergy
|
July 22, 2014
Casein-specific IL-4- and IL-13-secreting T cells: a tool to implement diagnosis of cow's milk allergy
B Michaud, J Aroulandom, N Baiz, et al.
Nature Genetics
|
October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
S Laberge-le Couteulx, H H Jung, P Labauge, et al.
Human Genetics
|
November 1, 1996
Age-dependent penetrance and mapping of the locus for juvenile and early-onset open-angle glaucoma on chromosome 1q (GLC1A) in a French family
A Meyer, A Béchetoille, F Valtot, et al.
Journal of Medical Genetics
|
July 1, 1997
Genetic heterogeneity of primary open angle glaucoma and ocular hypertension: linkage to GLC1A associated with an increased risk of severe glaucomatous optic neuropathy
A P Brézin, A Béchetoille, P Hamard, et al.
European Journal of Immunology
|
February 10, 2004
Exacerbated Th2-mediated airway inflammation and hyperresponsiveness in autoimmune diabetes-prone NOD mice: a critical role for CD1d-dependent NKT cells
Luiza M Araujo, Jean Lefort, Marie-Anne Nahori, et al.
Klinische Wochenschrift
|
January 15, 1988
Cyclosporin-associated nephropathy in patients with autoimmune diseases
M J Mihatsch, J F Bach, H M Coovadia, et al.
Lancet (London, England)
|
December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
A Joutel, K Vahedi, C Corpechot, et al.
Journal of Autoimmunity
|
March 14, 1998
Treatment of recalcitrant plaque psoriasis with a humanized non-depleting antibody to CD4
H Bachelez, B Flageul, L Dubertret, et al.
Human Molecular Genetics
|
November 5, 1997
Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucoma
M F Adam, A Belmouden, P Binisti, et al.
Page
of 48