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M L Lokki

Showing results (21-30 of 35) with videos related to

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Tissue Antigens|January 11, 2007
Human MHC region harbors both susceptibility and protective haplotypes for coronary artery diseaseA Palikhe, J Sinisalo, M Seppänen, et al.
Immunology|June 9, 1998
Molecular heterogeneity in deficiency of complement protein C2 type IX Wang, A Circolo, M L Lokki, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 27, 1999
Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genesM L Lokki, A Circolo, P Ahokas, et al.
Clinical Immunology and Immunopathology|December 1, 1996
Inherited complement C3 deficiency: reduced C3 mRNA and protein levels in a Laotian kindredL Singer, M L Van Hee, M L Lokki, et al.
Human Molecular Genetics|July 11, 2000
A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility alleleK Asumalahti, T Laitinen, R Itkonen-Vatjus, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 29, 2001
Complement C4 deficiency and HLA homozygosity in patients with frequent intraoral herpes simplex virus type 1 infectionsM Seppänen, M L Lokki, T Timonen, et al.
The Journal of Biological Chemistry|March 8, 1996
Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretionR A Wetsel, J Kulics, M L Lokki, et al.
Scandinavian Journal of Immunology|January 30, 2007
Complement and c4 null alleles in severe chronic adult periodontitisM Seppänen, M-L Lokki, I-L Notkola, et al.
Clinical and Experimental Immunology|August 24, 2017
C4B gene influences intestinal microbiota through complement activation in patients with paediatric-onset inflammatory bowel diseaseE Nissilä, K Korpela, A I Lokki, et al.
Tissue Antigens|April 4, 2008
Lymphotoxin alpha LTA+496C allele is a risk factor for periodontitis in patients with coronary artery diseaseA Palikhe, M-L Lokki, P J Pussinen, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Tissue Antigens|January 11, 2007
Human MHC region harbors both susceptibility and protective haplotypes for coronary artery diseaseA Palikhe, J Sinisalo, M Seppänen, et al.
Immunology|June 9, 1998
Molecular heterogeneity in deficiency of complement protein C2 type IX Wang, A Circolo, M L Lokki, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 27, 1999
Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genesM L Lokki, A Circolo, P Ahokas, et al.
Clinical Immunology and Immunopathology|December 1, 1996
Inherited complement C3 deficiency: reduced C3 mRNA and protein levels in a Laotian kindredL Singer, M L Van Hee, M L Lokki, et al.
Human Molecular Genetics|July 11, 2000
A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility alleleK Asumalahti, T Laitinen, R Itkonen-Vatjus, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 29, 2001
Complement C4 deficiency and HLA homozygosity in patients with frequent intraoral herpes simplex virus type 1 infectionsM Seppänen, M L Lokki, T Timonen, et al.
The Journal of Biological Chemistry|March 8, 1996
Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretionR A Wetsel, J Kulics, M L Lokki, et al.
Scandinavian Journal of Immunology|January 30, 2007
Complement and c4 null alleles in severe chronic adult periodontitisM Seppänen, M-L Lokki, I-L Notkola, et al.
Clinical and Experimental Immunology|August 24, 2017
C4B gene influences intestinal microbiota through complement activation in patients with paediatric-onset inflammatory bowel diseaseE Nissilä, K Korpela, A I Lokki, et al.
Tissue Antigens|April 4, 2008
Lymphotoxin alpha LTA+496C allele is a risk factor for periodontitis in patients with coronary artery diseaseA Palikhe, M-L Lokki, P J Pussinen, et al.
Pageof 4