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The New England Journal of Medicine
|
October 31, 1985
Genotyping with DNA probes in combined immunodeficiency syndrome with defective expression of HLA
T R Welch, L S Beischel
Human Immunology
|
July 1, 1993
A patient with 21-hydroxylase deficiency who exhibited only maternal major histocompatibility complex (MHC) antigens
T R Welch, L S Beischel
The American Journal of Pathology
|
October 1, 1991
Detection and cellular localization of human C4 gene expression in the renal tubular epithelial cells and other extrahepatic epithelial sources
D P Witte, T R Welch, L S Beischel
The Journal of Infectious Diseases
|
July 1, 1990
C4B deficiency: a risk factor for bacteremia with encapsulated organisms
N A Bishof, T R Welch, L S Beischel
Pediatric Nephrology (Berlin, Germany)
|
April 1, 1987
C4 isotype deficiency in IgA nephropathy
T R Welch, A Berry, L S Beischel
Human Immunology
|
December 1, 1989
Molecular genetics of C4B deficiency in IgA nephropathy
T R Welch, L S Beischel, E M Choi
The Journal of Clinical Investigation
|
September 1, 1993
Differential expression of complement C3 and C4 in the human kidney
T R Welch, L S Beischel, D P Witte
Arthritis and Rheumatism
|
September 1, 1995
Glomerulonephritis associated with complete deficiency of the fourth component of complement. Response to intravenous immunoglobulin
T R Welch, A J McAdams, L S Beischel
Kidney International
|
August 1, 1996
Regulated expression of complement factor B in the human kidney
T R Welch, L S Beischel, M Frenzke, et al.
The Journal of Clinical Investigation
|
August 1, 1990
Uniparental isodisomy 6 associated with deficiency of the fourth component of complement
T R Welch, L S Beischel, E Choi, et al.
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Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
The New England Journal of Medicine
|
October 31, 1985
Genotyping with DNA probes in combined immunodeficiency syndrome with defective expression of HLA
T R Welch, L S Beischel
Human Immunology
|
July 1, 1993
A patient with 21-hydroxylase deficiency who exhibited only maternal major histocompatibility complex (MHC) antigens
T R Welch, L S Beischel
The American Journal of Pathology
|
October 1, 1991
Detection and cellular localization of human C4 gene expression in the renal tubular epithelial cells and other extrahepatic epithelial sources
D P Witte, T R Welch, L S Beischel
The Journal of Infectious Diseases
|
July 1, 1990
C4B deficiency: a risk factor for bacteremia with encapsulated organisms
N A Bishof, T R Welch, L S Beischel
Pediatric Nephrology (Berlin, Germany)
|
April 1, 1987
C4 isotype deficiency in IgA nephropathy
T R Welch, A Berry, L S Beischel
Human Immunology
|
December 1, 1989
Molecular genetics of C4B deficiency in IgA nephropathy
T R Welch, L S Beischel, E M Choi
The Journal of Clinical Investigation
|
September 1, 1993
Differential expression of complement C3 and C4 in the human kidney
T R Welch, L S Beischel, D P Witte
Arthritis and Rheumatism
|
September 1, 1995
Glomerulonephritis associated with complete deficiency of the fourth component of complement. Response to intravenous immunoglobulin
T R Welch, A J McAdams, L S Beischel
Kidney International
|
August 1, 1996
Regulated expression of complement factor B in the human kidney
T R Welch, L S Beischel, M Frenzke, et al.
The Journal of Clinical Investigation
|
August 1, 1990
Uniparental isodisomy 6 associated with deficiency of the fourth component of complement
T R Welch, L S Beischel, E Choi, et al.
Page
of 2