Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Franz Petry"'
Publikováno v:
Experimental Parasitology. 126:304-309
Species of the genus Cryptosporidium are protozoan parasites (Apicomplexa) that cause gastroenteritis in animals and humans. Of these Cryptosporidium parvum and Cryptosporidium hominis are the major causative agents of human cryptosporidiosis. Wherea
Publikováno v:
Acta Tropica. 115:77-83
In this study, 1034 faecal samples from patients with diarrhoea were screened for Cryptosporidium oocysts. Samples were collected from nine different regions in Ethiopia. Of these, 79 samples (7.6%) were positive for Cryptosporidium by modified Ziehl
Autor:
Jun-ichi Furukawa, Shin-Ichiro Nishimura, Lucie Clementine Baudino, Yasuro Shinohara, J. Sjef Verbeek, Falk Nimmerjahn, Jeffery V. Ravetch, Franz Petry, Shozo Izui
Publikováno v:
Journal of Immunology, Vol. 181, No 6 (2008) pp. 4107-12
Four murine IgG subclasses display markedly different Fc-associated effector functions because of their differential binding to three activating IgG Fc receptors (FcγRI, FcγRIII, and FcγRIV) and C1q. Previous analysis of IgG subclass switch varian
Publikováno v:
Held, K, Thiel, S, Loos, M & Petry, F 2008, ' Increased susceptibility of complement factor B/C2 double knockout mice and mannan-binding lectin knockout mice to systemic infection with Candida albicans ', Molecular Immunology, vol. 45, no. 15, pp. 3934-41 . https://doi.org/10.1016/j.molimm.2008.06.021
Candida albicans is the major cause of systemic fungal infections in immunocompromised patients. We investigated the susceptibility of mice deficient in complement factor B and C2 (Bf/C2-/-), C1q (C1qa-/-), and mannan-binding lectin (MBL)-A (MBL-A) a
Publikováno v:
Immunobiology. 212:229-232
Autor:
Franz Petry, Michael Loos
Publikováno v:
Immunogenetics. 57:566-571
Hereditary complete deficiency of complement component C1q is a rare genetic disorder that is associated with severe recurrent infections and a high prevalence of lupus-erythematosus-like symptoms. In the past, several single nucleotide polymorphisms
Autor:
Josefina Cortes-Hernandez, Franz Petry, Michael Loos, Mark Walport, Liliane Fossati-Jimack, Shozo Izui, H. Terence Cook, Marina Botto
Publikováno v:
European Journal of Immunology, Vol. 34, No 12 (2004) pp. 3713-3722
C1q deficiency in both humans and mice is strongly associated with autoimmunity. We have previously shown that bone marrow transplantation (BMT) restored C1q levels in C1q-deficient (C1qa(-/-)) mice. Here, we studied the effect of BMT on autoimmunity
Publikováno v:
Parasitology. 128:269-282
Amylopectin is used for carbohydrate storage in different life-stages of a number of apicomplexan parasites. We have performed an ultrastructural analysis of amylopectin granules from the oocyst residual body and sporozoites ofCryptosporidium parvum.
Publikováno v:
Journal of Antimicrobial Chemotherapy. 52:359-364
With the spread of the human immunodeficiency virus in the early 1980s, cryptosporidiosis was regarded as an AIDS-defining disease. As an opportunistic pathogen, the intestinal parasite Cryptosporidium parvum became an important cause of chronic diar
Publikováno v:
Immunobiology. 201:347-355
Selective complete C1q deficiencies (SCDC1q) of the complement component C1q are rare genetic disorders with high prevalence of lupus-erythematosus-like symptoms and recurrent infections. Among the 41 published cases from 23 families, 10 derive from