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The Journal of Biological Chemistry
|
August 8, 2001
Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis
T Pan, M Colucci, B S Wong, et al.
Annals of Neurology
|
September 3, 2002
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy
Ayush Dagvadorj, Robert B Petersen, Hee Suk Lee, et al.
Plos One
|
December 17, 2011
Hyperdimensional analysis of amino acid pair distributions in proteins
Svend B Henriksen, Rasmus J Mortensen, Henrik M Geertz-Hansen, et al.
Human Antibodies and Hybridomas
|
January 1, 1990
Potential role of PHA in producing human monoclonal thyroid autoantibodies of different subclasses
S M McLachlan, N Fukuma, D Sarsero, et al.
Brain Research
|
March 30, 2001
Differential expression of cellular prion protein in mouse brain as detected with multiple anti-PrP monoclonal antibodies
T Liu, T Zwingman, R Li, et al.
Ugeskrift for Laeger
|
February 8, 1993
[AIDS--knowledge, behavior and attitude at the University of Aarhus in 1990. A questionnaire study]
M R Andersen, I Nielsen, H Nørrelund, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2005
Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases
Merete Bugge, Celia deLozier-Blanchet, Mads Bak, et al.
American Journal of Human Genetics
|
January 1, 1991
Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome
M B Petersen, A A Schinzel, F Binkert, et al.
International Journal of Obesity (2005)
|
June 6, 2013
DNA hypomethylation of inflammation-associated genes in adipose tissue of female mice after multigenerational high fat diet feeding
Y Ding, J Li, S Liu, et al.
Human Genetics
|
October 28, 1997
A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
O Bartsch, G K Hinkel, M B Petersen, et al.
Page
of 124
Search research articles
Search
Showing results (821-830 of 1,237) with videos related to
Sort By:
Page
of 124
The Journal of Biological Chemistry
|
August 8, 2001
Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis
T Pan, M Colucci, B S Wong, et al.
Annals of Neurology
|
September 3, 2002
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy
Ayush Dagvadorj, Robert B Petersen, Hee Suk Lee, et al.
Plos One
|
December 17, 2011
Hyperdimensional analysis of amino acid pair distributions in proteins
Svend B Henriksen, Rasmus J Mortensen, Henrik M Geertz-Hansen, et al.
Human Antibodies and Hybridomas
|
January 1, 1990
Potential role of PHA in producing human monoclonal thyroid autoantibodies of different subclasses
S M McLachlan, N Fukuma, D Sarsero, et al.
Brain Research
|
March 30, 2001
Differential expression of cellular prion protein in mouse brain as detected with multiple anti-PrP monoclonal antibodies
T Liu, T Zwingman, R Li, et al.
Ugeskrift for Laeger
|
February 8, 1993
[AIDS--knowledge, behavior and attitude at the University of Aarhus in 1990. A questionnaire study]
M R Andersen, I Nielsen, H Nørrelund, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2005
Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases
Merete Bugge, Celia deLozier-Blanchet, Mads Bak, et al.
American Journal of Human Genetics
|
January 1, 1991
Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome
M B Petersen, A A Schinzel, F Binkert, et al.
International Journal of Obesity (2005)
|
June 6, 2013
DNA hypomethylation of inflammation-associated genes in adipose tissue of female mice after multigenerational high fat diet feeding
Y Ding, J Li, S Liu, et al.
Human Genetics
|
October 28, 1997
A large family with subtelomeric translocation t(18;21)(q23;q22.1) and molecular breakpoint in the Down syndrome critical region
O Bartsch, G K Hinkel, M B Petersen, et al.
Page
of 124