Search research articles
Contact Us
Filters
Showing results (91-100 of 118) with videos related to
Page
of 12
Sort By:
American Journal of Ophthalmology
|
July 1, 1997
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
S Andréasson, V Ponjavic, M Abrahamson, et al.
Biochemical and Biophysical Research Communications
|
May 15, 1989
Rapid cloning of rearranged immunoglobulin genes from human hybridoma cells using mixed primers and the polymerase chain reaction
J W Larrick, L Danielsson, C A Brenner, et al.
Journal of Periodontal Research
|
November 3, 2012
Cleavage of IgG1 in gingival crevicular fluid is associated with the presence of Porphyromonas gingivalis
A Guentsch, C Hirsch, W Pfister, et al.
Molecular Pathology : MP
|
April 8, 1999
Intracellular accumulation of the amyloidogenic L68Q variant of human cystatin C in NIH/3T3 cells
M Bjarnadottir, B S Wulff, M Sameni, et al.
American Journal of Hematology
|
February 1, 1993
Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders
G M Abrahamson, K Rack, D G Oscier, et al.
The Journal of Biological Chemistry
|
July 25, 1993
Human cystatin D. cDNA cloning, characterization of the Escherichia coli expressed inhibitor, and identification of the native protein in saliva
J P Freije, M Balbín, M Abrahamson, et al.
Archives of Biochemistry and Biophysics
|
February 20, 1995
Synthesis and secretion of procathepsin B and cystatin C by human bronchial epithelial cells in vitro: modulation of cathepsin B activity by neutrophil elastase
D Burnett, M Abrahamson, J L Devalia, et al.
Biomedica Biochimica Acta
|
January 1, 1991
Regulation of cystatin C activity by serine proteinases
M Abrahamson, D J Buttle, R W Mason, et al.
Ophthalmic Genetics
|
December 1, 1995
Phenotype variations within a choroideremia family lacking the entire CHM gene
V Ponjavic, M Abrahamson, S Andréasson, et al.
Cancer Genetics and Cytogenetics
|
May 1, 1991
Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor
G M Abrahamson, K Rack, V J Buckle, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 118) with videos related to
Sort By:
Page
of 12
American Journal of Ophthalmology
|
July 1, 1997
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
S Andréasson, V Ponjavic, M Abrahamson, et al.
Biochemical and Biophysical Research Communications
|
May 15, 1989
Rapid cloning of rearranged immunoglobulin genes from human hybridoma cells using mixed primers and the polymerase chain reaction
J W Larrick, L Danielsson, C A Brenner, et al.
Journal of Periodontal Research
|
November 3, 2012
Cleavage of IgG1 in gingival crevicular fluid is associated with the presence of Porphyromonas gingivalis
A Guentsch, C Hirsch, W Pfister, et al.
Molecular Pathology : MP
|
April 8, 1999
Intracellular accumulation of the amyloidogenic L68Q variant of human cystatin C in NIH/3T3 cells
M Bjarnadottir, B S Wulff, M Sameni, et al.
American Journal of Hematology
|
February 1, 1993
Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders
G M Abrahamson, K Rack, D G Oscier, et al.
The Journal of Biological Chemistry
|
July 25, 1993
Human cystatin D. cDNA cloning, characterization of the Escherichia coli expressed inhibitor, and identification of the native protein in saliva
J P Freije, M Balbín, M Abrahamson, et al.
Archives of Biochemistry and Biophysics
|
February 20, 1995
Synthesis and secretion of procathepsin B and cystatin C by human bronchial epithelial cells in vitro: modulation of cathepsin B activity by neutrophil elastase
D Burnett, M Abrahamson, J L Devalia, et al.
Biomedica Biochimica Acta
|
January 1, 1991
Regulation of cystatin C activity by serine proteinases
M Abrahamson, D J Buttle, R W Mason, et al.
Ophthalmic Genetics
|
December 1, 1995
Phenotype variations within a choroideremia family lacking the entire CHM gene
V Ponjavic, M Abrahamson, S Andréasson, et al.
Cancer Genetics and Cytogenetics
|
May 1, 1991
Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor
G M Abrahamson, K Rack, V J Buckle, et al.
Page
of 12