science
plus
.abes.fr
|
explorer
À propos de :
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_22/w
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
bibo:Issue
, within Data Space :
scienceplus.abes.fr
associated with source
document(s)
Type:
work
Issue
New Facet based on Instances of this Class
Attributs
Valeurs
type
work
Issue
Is Part Of
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12
has manifestation of work
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_22/m/web
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_22/m/print
Date Copyrighted
2003
issue
22
is
Is Part Of
of
Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos
Mutation of a transcriptional motif of a distant regulatory element reduces the expression of embryonic and fetal globin genes
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
Gene expression variation in the adult human retina
Genetic background regulates β-amyloid precursor protein processing and β-amyloid deposition in the mouse
RING finger 1 mutations in Parkin produce altered localization of the protein
Inducible mEDA-A1 transgene mediates sebaceous gland hyperplasia and differential formation of two types of mouse hair follicles
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
Interaction between a peroxisome proliferator-activated receptor γ gene polymorphism and dietary fat intake in relation to body mass
NSDHL, an enzyme involved in cholesterol biosynthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid droplets
E-cadherin germline missense mutations and cell phenotype: evidence for the independence of cell invasion on the motile capabilities of the cells
Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains
Co-duplication of olfactory receptor and MHC class I genes in the mouse major histocompatibility complex
Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda
The HLA class III subregion is responsible for an increased breast cancer risk
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata