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Structure (London, England : 1993)
|
September 21, 2000
Crystal structure and mutational analysis of the Saccharomyces cerevisiae cell cycle regulatory protein Cks1: implications for domain swapping, anion binding and protein interactions
Y Bourne, M H Watson, A S Arvai, et al.
Antonie Van Leeuwenhoek
|
January 1, 1987
Three dimensional structure of bacterial pili
H E Parge, D E McRee, M A Capozza, et al.
Journal of Science and Medicine in Sport
|
January 5, 2019
Gross motor skills of South African preschool-aged children across different income settings
S A Tomaz, R A Jones, T Hinkley, et al.
Infection and Immunity
|
February 1, 1996
Assembly and antigenicity of the Neisseria gonorrhoeae pilus mapped with antibodies
K T Forest, S L Bernstein, E D Getzoff, et al.
Journal of Molecular Biology
|
September 6, 1996
A mutation in the human cyclin-dependent kinase interacting protein, CksHs2, interferes with cyclin-dependent kinase binding and biological function, but preserves protein structure and assembly
M H Watson, Y Bourne, A S Arvai, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 24, 1995
Crystal structure of the cell cycle-regulatory protein suc1 reveals a beta-hinge conformational switch
Y Bourne, A S Arvai, S L Bernstein, et al.
American Journal of Human Genetics
|
June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
Z M Ahmed, S Riazuddin, S L Bernstein, et al.
Molecular Vision
|
October 31, 2000
Clusterin protein diversity in the primate eye
P Wong, B A Pfeffer, S L Bernstein, et al.
The Journal of Biological Chemistry
|
February 5, 1990
Biochemical purification and crystallographic characterization of the fiber-forming protein pilin from Neisseria gonorrhoeae
H E Parge, S L Bernstein, C D Deal, et al.
American Journal of Human Genetics
|
November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
J M Bork, L M Peters, S Riazuddin, et al.
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of 3
Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 30 results.
Structure (London, England : 1993)
|
September 21, 2000
Crystal structure and mutational analysis of the Saccharomyces cerevisiae cell cycle regulatory protein Cks1: implications for domain swapping, anion binding and protein interactions
Y Bourne, M H Watson, A S Arvai, et al.
Antonie Van Leeuwenhoek
|
January 1, 1987
Three dimensional structure of bacterial pili
H E Parge, D E McRee, M A Capozza, et al.
Journal of Science and Medicine in Sport
|
January 5, 2019
Gross motor skills of South African preschool-aged children across different income settings
S A Tomaz, R A Jones, T Hinkley, et al.
Infection and Immunity
|
February 1, 1996
Assembly and antigenicity of the Neisseria gonorrhoeae pilus mapped with antibodies
K T Forest, S L Bernstein, E D Getzoff, et al.
Journal of Molecular Biology
|
September 6, 1996
A mutation in the human cyclin-dependent kinase interacting protein, CksHs2, interferes with cyclin-dependent kinase binding and biological function, but preserves protein structure and assembly
M H Watson, Y Bourne, A S Arvai, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 24, 1995
Crystal structure of the cell cycle-regulatory protein suc1 reveals a beta-hinge conformational switch
Y Bourne, A S Arvai, S L Bernstein, et al.
American Journal of Human Genetics
|
June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
Z M Ahmed, S Riazuddin, S L Bernstein, et al.
Molecular Vision
|
October 31, 2000
Clusterin protein diversity in the primate eye
P Wong, B A Pfeffer, S L Bernstein, et al.
The Journal of Biological Chemistry
|
February 5, 1990
Biochemical purification and crystallographic characterization of the fiber-forming protein pilin from Neisseria gonorrhoeae
H E Parge, S L Bernstein, C D Deal, et al.
American Journal of Human Genetics
|
November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
J M Bork, L M Peters, S Riazuddin, et al.
Page
of 3