Home
About
Overview
Sharing Data
ORCID
Help
History (1)
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.
See All Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 2001 May 31; 411(6837):603-6.
View in:
PubMed
subject areas
Adult
Alleles
Amino Acid Sequence
Base Sequence
Carrier Proteins
Case-Control Studies
Cell Line
Child
Crohn Disease
Cytosine
DNA
Female
Frameshift Mutation
Gene Frequency
Genetic Predisposition to Disease
Heterozygote
Homozygote
Humans
Intracellular Signaling Peptides and Proteins
Lipopolysaccharides
Male
Molecular Sequence Data
Mutagenesis, Insertional
NF-kappa B
Nod2 Signaling Adaptor Protein
Polymerase Chain Reaction
Protein Structure, Tertiary
Proteins
authors with profiles
Stephen B. Hanauer
Dan Liviu Nicolae
Barbara S. Kirschner