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British Journal of Rheumatology|May 1, 1996
Expression of the multidrug resistance glycoprotein 170 in the peripheral blood lymphocytes of rheumatoid arthritis patients. The percentage of lymphocytes expressing glycoprotein 170 is increased in patients treated with prednisoloneJ F Maillefert, M Maynadie, J G Tebib, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 20, 2008
Trends of methicillin-resistant Staphylococcus aureus (MRSA) and Enterobacteriaceae-producing extended-spectrum beta-lactamase (ESBLE) in eastern France: a three-year multi-centre incidence studyX Bertrand, L Mouchot, M Jebabli, et al.
AIDS (London, England)|March 31, 1998
Does hepatitis C virus co-infection accelerate clinical and immunological evolution of HIV-infected patients?L Piroth, M Duong, C Quantin, et al.
Nature Genetics|May 1, 1996
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndromeE Maestrini, A P Monaco, J A McGrath, et al.
Gene Therapy|September 23, 2011
Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosaM Endo, P W Zoltick, A Radu, et al.
The British Journal of Dermatology|December 22, 1999
Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1F J Smith, M Del Monaco, P M Steijlen, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1991
Human type VII collagen: cDNA cloning and chromosomal mapping of the geneM G Parente, L C Chung, J Ryynänen, et al.
Journal of Virology|February 25, 2011
Qualitative and quantitative analysis of the binding of GII.4 norovirus variants onto human blood group antigensA de Rougemont, N Ruvoen-Clouet, B Simon, et al.
Experimental Dermatology|June 6, 2000
Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratodermaF J Smith, M P Fisher, E Healy, et al.
Clinical and Experimental Dermatology|February 24, 2018
Seven novel COL7A1 mutations identified in patients with recessive dystrophic epidermolysis bullosa from MexicoA H Saeidian, L Youssefian, M G Moreno Trevino, et al.
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