science
plus
.abes.fr
|
explorer
À propos de :
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_1/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/2001/volume_10
has manifestation of work
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_1/m/web
http://hub.abes.fr/oup/periodical/hmg/2001/volume_10/issue_1/m/print
Date Copyrighted
2001
issue
1
is
Is Part Of
of
Palmitoyl protein thioesterase (PPT) localizes into synaptosomes and synaptic vesicles in neurons: implications for infantile neuronal ceroid lipofuscinosis (INCL)
The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia
Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues
The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy
The kyphoscoliosis (ky) mouse is deficient in hypertrophic responses and is caused by a mutation in a novel muscle-specific protein
The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death
Methylation profiles of DXPas34 during the onset of X-inactivation
Autosomal dominant transmission of GLUT1 deficiency
A germline deletion of p14ARF but not CDKN2A in a melanoma-neural system tumour syndrome family
Corrigendum
X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications
Erratum
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata