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H R Colten

Showing results (181-190 of 200) with videos related to

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The Journal of Biological Chemistry|June 25, 1985
Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1E C Mantzouranis, S B Dowton, A S Whitehead, et al.
The Journal of Clinical Investigation|April 1, 1994
A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindredsL M Nogee, G Garnier, H C Dietz, et al.
The Journal of Pediatrics|September 1, 1994
Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacementA Hamvas, F S Cole, D E deMello, et al.
The New England Journal of Medicine|July 4, 1985
The molecular basis for genetic deficiency of the second component of human complementF S Cole, A S Whitehead, H S Auerbach, 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.
Biochemistry|June 4, 1985
Human serum amyloid A (SAA): biosynthesis and postsynthetic processing of preSAA and structural variants defined by complementary DNAJ D Sipe, H R Colten, G Goldberger, et al.
Pediatrics|March 4, 2000
Population-based estimates of surfactant protein B deficiencyF S Cole, A Hamvas, P Rubinstein, et al.
The Journal of Clinical Investigation|September 1, 1986
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variantsP M Schneider, M C Carroll, C A Alper, et al.
Clinical Immunology and Immunopathology|November 1, 1977
Homozygous C3 deficiency: detection of C3 by radioimmunoassayA E Davis, J S Davis, A R Rabson, et al.
The Journal of Experimental Medicine|September 1, 1982
Cooperative interaction of factor B and other complement components with mononuclear cells in the antibody-independent lysis of xenogeneic erythrocytesR E Hall, R M Blaese, A E Davis, et al.
Pageof 20

Showing results (181-190 of 200) with videos related to

Sort By:
Pageof 20
The Journal of Biological Chemistry|June 25, 1985
Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1E C Mantzouranis, S B Dowton, A S Whitehead, et al.
The Journal of Clinical Investigation|April 1, 1994
A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindredsL M Nogee, G Garnier, H C Dietz, et al.
The Journal of Pediatrics|September 1, 1994
Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacementA Hamvas, F S Cole, D E deMello, et al.
The New England Journal of Medicine|July 4, 1985
The molecular basis for genetic deficiency of the second component of human complementF S Cole, A S Whitehead, H S Auerbach, 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.
Biochemistry|June 4, 1985
Human serum amyloid A (SAA): biosynthesis and postsynthetic processing of preSAA and structural variants defined by complementary DNAJ D Sipe, H R Colten, G Goldberger, et al.
Pediatrics|March 4, 2000
Population-based estimates of surfactant protein B deficiencyF S Cole, A Hamvas, P Rubinstein, et al.
The Journal of Clinical Investigation|September 1, 1986
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variantsP M Schneider, M C Carroll, C A Alper, et al.
Clinical Immunology and Immunopathology|November 1, 1977
Homozygous C3 deficiency: detection of C3 by radioimmunoassayA E Davis, J S Davis, A R Rabson, et al.
The Journal of Experimental Medicine|September 1, 1982
Cooperative interaction of factor B and other complement components with mononuclear cells in the antibody-independent lysis of xenogeneic erythrocytesR E Hall, R M Blaese, A E Davis, et al.
Pageof 20