about
Multidirectional chromosome painting substantiates the occurrence of extensive genomic reshuffling within AccipitriformesCharacterization of the atypical karyotype of the black-winged kite Elanus caeruleus (Falconiformes: Accipitridae) by means of classical and molecular cytogenetic techniques.Non-coding RNAs revealed during identification of genes involved in chicken immune responses.Genetic analysis of local Vietnamese chickens provides evidence of gene flow from wild to domestic populations.Revealing fine scale subpopulation structure in the Vietnamese H'Mong cattle breed for conservation purposes.Vietnamese chickens: a gate towards Asian genetic diversitySex-linked barring in chickens is controlled by the CDKN2A /B tumour suppressor locus.Avian genomes: different karyotypes but a similar distribution of the GC-richest chromosome regions at interphase.Structural and functional annotation of the porcine immunome.Preimplantation genetic diagnosis in Welsh pony embryos after biopsy and cryopreservation.The evolution of Sex-linked barring alleles in chickens involves both regulatory and coding changes in CDKN2AThe lavender plumage colour in Japanese quail is associated with a complex mutation in the region of MLPH that is related to differences in growth, feed consumption and body temperatureTranscriptome-wide investigation of genomic imprinting in chickenDetection of QTL controlling digestive efficiency and anatomy of the digestive tract in chicken fed a wheat-based diet.Chicken domestication: from archeology to genomics.Transcriptomes of whole blood and PBMC in chickens.A novel chicken lung epithelial cell line: characterization and response to low pathogenicity avian influenza virus.A high-density SNP panel reveals extensive diversity, frequent recombination and multiple recombination hotspots within the chicken major histocompatibility complex B region between BG2 and CD1A1.Genome-wide association study and biological pathway analysis of the Eimeria maxima response in broilers.Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species.Annotation and genetic diversity of the chicken collagenous lectins.Sex and PRNP genotype determination in preimplantation caprine embryos.QTL detection for coccidiosis (Eimeria tenella) resistance in a Fayoumi × Leghorn F₂ cross, using a medium-density SNP panel.Characterisation of a cluster of TRIM-B30.2 genes in the chicken MHC B locus.Cytogenetic repartition of chicken CR1 sequences evidenced by PRINS in Galliformes and some other birds.Antibody responses to keyhole limpet hemocyanin, lipopolysaccharide, and Newcastle Disease virus vaccine in F2 and backcrosses of white Leghorn lines selected for two different immune response traits.Assessing the quality of donor cells: karyotyping methods.A global analysis of molecular markers and phenotypic traits in local chicken breeds in Taiwan.The Dark brown plumage color in chickens is caused by an 8.3-kb deletion upstream of SOX10.Molecular genotype investigation of the Gallus gallus major histocompatibility complex.Immunome differences between porcine ileal and jejunal Peyer's patches revealed by global transcriptome sequencing of gut-associated lymphoid tissues.Genetic and morphometric characterization of a local Vietnamese Swamp Buffalo populationUsing molecular markers and multivariate methods to study the genetic diversity of local European and Asian chicken breedsLarge-scale investigation of the parameters in response to Eimeria maxima challenge in broilersDelayed-type hypersensitivity response to KLH in F2 and backcrosses of two immune selected chicken lines: effect of immunisation and selectionComparison of SNPs and microsatellites for assessing the genetic structure of chicken populationsA missense mutation in TYRP1 causes the chocolate plumage color in chicken and alters melanosome structure
P50
Q28607250-2769B965-CDC5-4C3F-8D2D-056CF8B7C3D0Q31152794-81261524-F34B-4C7A-B93D-E26C1B09D5CDQ33384471-D34CA420-9FD4-40A2-B3B9-49D4B315BB30Q33398677-50C2FF7F-EB79-419A-9063-8B9AC438E092Q33595449-A61CA51C-8390-4BBD-8250-2183E8CAFEEAQ33611183-542AB72E-F917-409E-9527-1D744355972BQ34108991-E59CD744-2718-4001-9D8B-4678CF491215Q34473357-D35A6FB3-FEA0-41C4-8CDC-E507FE0F15ECQ34724017-7CFC5E16-5138-412D-B625-B1B1C327E666Q35862025-EABBEC06-65A1-4FEB-8E54-6CE063B969B9Q36339738-64477910-3A1C-4D8A-B072-F13D0793D4F5Q36356244-64AD1D78-0782-4527-8321-3E110EBD728DQ37680361-3D37BF03-138A-42E0-BC4B-EE00B5748036Q37724079-796F42D8-DF41-48C1-970B-0EE65B307C87Q37850131-A484E963-F90D-4EBE-A511-7048FBBBC626Q38981010-3431861F-EA54-4E43-A300-B96B196B8CCDQ39545194-B7D21173-DC25-4982-9250-40CD97525B48Q40840763-78345BEB-69C4-48B6-A53F-47710C21E70FQ40894981-B7D0F850-5A70-4EC6-9505-52E8F8256B0EQ41126905-A9F17DD3-A132-41B6-9F63-4C94BB57734FQ41344895-BFD2113B-CCF3-4C5B-A1C7-8AE299DE286DQ41608529-1182218F-DABE-49A6-A20D-6DF73ABFCC70Q41982773-650DAF1D-45FB-471D-AC4D-99A5BFFF51F8Q42649215-F764CA65-A0C0-482D-B23F-312201DFB504Q42671143-AC3FAF8B-C340-4B27-AA82-CD641BE07BC4Q45402866-05FD3904-B099-46A3-BA45-7DDC67E70945Q48593109-6A5D516C-B58F-428F-B493-5DCB779433B4Q48638896-ECF19178-B099-42C7-95A7-8A3740260CE4Q50549428-A385E47E-E48A-42EC-85AD-E39973F17F2AQ54514487-38C01AF4-F00D-4B49-A555-9A3CC3EF59B6Q55399078-24DA6BE9-D381-489B-8B11-4C947DA2FFD4Q60535793-9103D5D7-9B73-407B-AFB7-DC9292D85D66Q60535795-2C6C931F-6399-4C41-B795-78FBE946335AQ61936137-6DD7DE29-EA2A-486E-8EE0-5343198E57C9Q82075076-0729A2A6-3234-4CFF-94F7-BAC7D073D1F8Q83873441-2CCCD5B0-7902-40F3-9DB5-891AFE98DB7EQ93238414-64990DEF-E50A-4039-A396-76C2CC39833F
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Bertrand Bed'Hom
@ast
Bertrand Bed'Hom
@en
Bertrand Bed'Hom
@es
Bertrand Bed'Hom
@nl
Bertrand Bed'Hom
@sl
type
label
Bertrand Bed'Hom
@ast
Bertrand Bed'Hom
@en
Bertrand Bed'Hom
@es
Bertrand Bed'Hom
@nl
Bertrand Bed'Hom
@sl
prefLabel
Bertrand Bed'Hom
@ast
Bertrand Bed'Hom
@en
Bertrand Bed'Hom
@es
Bertrand Bed'Hom
@nl
Bertrand Bed'Hom
@sl
P1053
G-7313-2011
P106
P1153
23570344600
P31
P496
0000-0002-0825-0886