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The Journal of Cell Biology
|
April 1, 1990
The human alpha 2-macroglobulin receptor: identification of a 420-kD cell surface glycoprotein specific for the activated conformation of alpha 2-macroglobulin
J D Ashcom, S E Tiller, K Dickerson, et al.
Frontiers in Immunology
|
September 21, 2017
Facile Affinity Maturation of Antibody Variable Domains Using Natural Diversity Mutagenesis
Kathryn E Tiller, Ratul Chowdhury, Tong Li, et al.
Journal of Family Medicine and Primary Care
|
July 26, 2016
Domestic violence in the Solomon Islands
Mikaela A Ming, Molly G Stewart, Rose E Tiller, et al.
American Journal of Human Genetics
|
June 13, 1998
Marshall syndrome associated with a splicing defect at the COL11A1 locus
A J Griffith, L K Sprunger, D A Sirko-Osadsa, et al.
The Journal of Biological Chemistry
|
November 5, 1992
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesis
R Bogaert, G E Tiller, M A Weis, et al.
Pediatrics
|
September 1, 1981
Infant pneumonitis associated with cytomegalovirus, Chlamydia, Pneumocystis, and Ureaplasma: a prospective study
S Stagno, D M Brasfield, M B Brown, et al.
Protein Engineering, Design & Selection : PEDS
|
September 20, 2015
Co-evolution of affinity and stability of grafted amyloid-motif domain antibodies
Mark C Julian, Christine C Lee, Kathryn E Tiller, et al.
American Journal of Human Genetics
|
February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenita
G E Tiller, M A Weis, P A Polumbo, et al.
The Journal of Biological Chemistry
|
November 26, 2015
Design and Optimization of Anti-amyloid Domain Antibodies Specific for β-Amyloid and Islet Amyloid Polypeptide
Christine C Lee, Mark C Julian, Kathryn E Tiller, et al.
Nature Genetics
|
August 4, 1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
A K Gedeon, A Colley, R Jamieson, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 60) with videos related to
Sort By:
Page
of 6
The Journal of Cell Biology
|
April 1, 1990
The human alpha 2-macroglobulin receptor: identification of a 420-kD cell surface glycoprotein specific for the activated conformation of alpha 2-macroglobulin
J D Ashcom, S E Tiller, K Dickerson, et al.
Frontiers in Immunology
|
September 21, 2017
Facile Affinity Maturation of Antibody Variable Domains Using Natural Diversity Mutagenesis
Kathryn E Tiller, Ratul Chowdhury, Tong Li, et al.
Journal of Family Medicine and Primary Care
|
July 26, 2016
Domestic violence in the Solomon Islands
Mikaela A Ming, Molly G Stewart, Rose E Tiller, et al.
American Journal of Human Genetics
|
June 13, 1998
Marshall syndrome associated with a splicing defect at the COL11A1 locus
A J Griffith, L K Sprunger, D A Sirko-Osadsa, et al.
The Journal of Biological Chemistry
|
November 5, 1992
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesis
R Bogaert, G E Tiller, M A Weis, et al.
Pediatrics
|
September 1, 1981
Infant pneumonitis associated with cytomegalovirus, Chlamydia, Pneumocystis, and Ureaplasma: a prospective study
S Stagno, D M Brasfield, M B Brown, et al.
Protein Engineering, Design & Selection : PEDS
|
September 20, 2015
Co-evolution of affinity and stability of grafted amyloid-motif domain antibodies
Mark C Julian, Christine C Lee, Kathryn E Tiller, et al.
American Journal of Human Genetics
|
February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenita
G E Tiller, M A Weis, P A Polumbo, et al.
The Journal of Biological Chemistry
|
November 26, 2015
Design and Optimization of Anti-amyloid Domain Antibodies Specific for β-Amyloid and Islet Amyloid Polypeptide
Christine C Lee, Mark C Julian, Kathryn E Tiller, et al.
Nature Genetics
|
August 4, 1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
A K Gedeon, A Colley, R Jamieson, et al.
Page
of 6