Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laure Case"'
Autor:
Samantha Meadows, Crystal Davis, Suzanne R. Burstein, Corey Anderson, Aamir Zuberi, Kirsten Bredvik, Teresa A. Milner, Jalia Dash, Alessandra Piersigilli, Giovanni Manfredi, Cathleen M. Lutz, Hibiki Kawamata, Laure Case
Publikováno v:
Acta Neuropathol
Mutations in coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10), a mitochondrial protein of unknown function, cause a disease spectrum with clinical features of motor neuron disease, dementia, myopathy and cardiomyopathy. To investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99e5af000f4c279f688e57bb9336a44
https://europepmc.org/articles/PMC6571048/
https://europepmc.org/articles/PMC6571048/
Publikováno v:
The Journal of Immunology. 202:132.14-132.14
Systemic Lupus Erythematosus is a chronic autoimmune disease that causes systemic damage throughout the body and is characterized by a broad spectrum of clinical manifestations. The pathogenic mechanisms underlying the disease remain unclear, but are
Publikováno v:
The Journal of Immunology. 188:123.14-123.14
The histamine H1 receptor (Hrh1/H1R) was identified as a shared autoimmune disease (SAID) gene in experimental allergic encephalomyelitis (EAE) and autoimmune orchitis, the principal AI models of multiple sclerosis (MS) and idiopathic male infertilit
Autor:
Leon Toussaint, Laure Case, Stephanie Terrizzi, Jeffrey Ericson, Christophe Benoist, Cory Teuscher, Laurent Brossay
Publikováno v:
The Journal of Immunology. 186:153.44-153.44
In previous studies, we identified a mouse strain, B6.Ynkt, in which only males were deficient in iNKT cells and demonstrated that the deficiency was linked to Y-chromosome factors. We reasoned that the deficiency could be due to either a consomic ef
Publikováno v:
The Journal of Immunology. 184:143.51-143.51
Histamine (HA) is a key regulator of experimental allergic encephalomyelitis (EAE), the autoimmune disease model of multiple sclerosis (MS). Histidine decarboxylase deficient mice (HDCKO), which are unable to synthesize HA, exhibit more severe EAE an