about
Dynamic instability of the major urinary protein gene family revealed by genomic and phenotypic comparisons between C57 and 129 strain miceGenetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.The DNA sequence and biological annotation of human chromosome 1The DNA sequence and comparative analysis of human chromosome 10The DNA sequence and analysis of human chromosome 6The DNA sequence and comparative analysis of human chromosome 20The DNA sequence of the human X chromosomeDNA sequence and analysis of human chromosome 9The genome sequence of taurine cattle: a window to ruminant biology and evolutionThe Vertebrate Genome Annotation (Vega) databaseCurrent status and new features of the Consensus Coding Sequence databaseTracking and coordinating an international curation effort for the CCDS ProjectThe DNA sequence and analysis of human chromosome 13The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcriptsVariation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype ProjectThe consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomesDNA sequence of human chromosome 17 and analysis of rearrangement in the human lineageIntegrative annotation of 21,037 human genes validated by full-length cDNA clonesThe GENCODE human gene setThe transcriptional landscape of the mammalian genomeAnalysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAsIdentification of putative noncoding RNAs among the RIKEN mouse full-length cDNA collectionA novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the müllerian ductFunctional annotation of a full-length mouse cDNA collectionPseudo-messenger RNA: phantoms of the transcriptomeDiscovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.Meeting report: a workshop on Best Practices in Genome Annotation.The Vertebrate Genome Annotation browser 10 years onGenomic anatomy of the Tyrp1 (brown) deletion complex.The vertebrate genome annotation (Vega) databaseStructural and functional annotation of the porcine immunome.Gene map of the extended human MHC.Sequencing and characterization of the FVB/NJ mouse genome.Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183).Sequencing and comparative analysis of the gorilla MHC genomic sequenceOrganization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouse.Complete MHC haplotype sequencing for common disease gene mapping.The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.Expression of cell growth and bone specific genes at single cell resolution during development of bone tissue-like organization in primary osteoblast cultures.Progressive development of the rat osteoblast phenotype in vitro: reciprocal relationships in expression of genes associated with osteoblast proliferation and differentiation during formation of the bone extracellular matrix.
P50
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description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Laurens G Wilming
@en
Laurens G Wilming
@es
Laurens G Wilming
@nl
Laurens G Wilming
@sl
Laurens Wilming
@fr
type
label
Laurens G Wilming
@en
Laurens G Wilming
@es
Laurens G Wilming
@nl
Laurens G Wilming
@sl
Laurens Wilming
@fr
prefLabel
Laurens G Wilming
@en
Laurens G Wilming
@es
Laurens G Wilming
@nl
Laurens G Wilming
@sl
Laurens Wilming
@fr
P106
P21
P2456
P31
P496
0000-0002-4154-7358