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Titolo Data di pubblicazione Autori File
NUCLEOTIDE-SEQUENCE OF THE CDNA FOR LECITHIN-CHOLESTEROL ACYL TRANSFERASE (LCAT) FROM THE RAT 1-gen-1990 MERONI, GERMANA +
DEFINITION OF THE TRANSCRIPTION INITIATION SITE OF HUMAN PLASMINOGEN GENE IN LIVER AND NON HEPATIC CELL-LINES 1-gen-1990 MERONI, GERMANA +
FUNCTIONAL-ANALYSIS OF THE HUMAN LECITHIN-CHOLESTEROL ACYL TRANSFERASE GENE PROMOTER 1-gen-1991 MERONI, GERMANA +
A CLUSTER OF SULFATASE GENES ON XP22.3 - MUTATIONS IN CHONDRODYSPLASIA PUNCTATA (CDPX) AND IMPLICATIONS FOR WARFARIN EMBRYOPATHY 1-gen-1995 MERONI, GERMANA +
Motifs resembling hepatocyte nuclear factor 1 and activator protein 3 mediate the tissue specificity of the human plasminogen gene 1-gen-1996 MERONI, GERMANA +
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region 1-gen-1996 MERONI, GERMANA +
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor 1-gen-1997 MERONI, GERMANA +
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE gene 1-gen-1997 MERONI, GERMANA +
Comparative mapping of Xp22 genes in hominoids - Evolutionary linear instability of their Y homologues 1-gen-1997 MERONI, GERMANA +
The sulfatase gene family 1-gen-1997 MERONI, GERMANA +
Assignement of the E1A-regulated transcription factor gene(E4F17 to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids 1-gen-1998 MERONI, GERMANADEL SAL, GIANNINO +
Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata 1-gen-1998 MERONI, GERMANA +
The human ROX gene: Genomic structure and mutation analysis in human breast tumors 1-gen-1998 MERONI, GERMANA +
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle 1-gen-1999 MERONI, GERMANA +
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development 1-gen-1999 MERONI, GERMANA +
Mlx, a new Max-Like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? 1-gen-2000 MERONI, GERMANA +
The tripartite motif family identifies cell compartments 1-gen-2001 MERONI, GERMANA +
Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4 1-gen-2001 MERONI, GERMANA +
TRIM9 is specifically expressed in the embryonic and adult nervous system 1-gen-2002 MERONI, GERMANA +
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) 1-gen-2002 MERONI, GERMANA +
Mostrati risultati da 1 a 20 di 66
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