about
Ectopic KIT copy number variation underlies impaired migration of primordial germ cells associated with gonadal hypoplasia in cattle (Bos taurus)A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus).FISH mapping of 10 canine BAC clones harbouring genes and microsatellites in the arctic fox and the Chinese raccoon dog genomes.Cytogenetic mapping of eight genes encoding fatty acid binding proteins (FABPs) in the pig genome.Missense mutations and polymorphisms of the MC4R gene in Polish obese children and adolescents in relation to the relative body mass indexThe first case of 38,XX (SRY-positive) disorder of sex development in a cat.Effect of three common SNPs in 5'-flanking region of LEP and ADIPOQ genes on their expression in Polish obese children and adolescents.Copy number variation in the region harboring SOX9 gene in dogs with testicular/ovotesticular disorder of sex development (78,XX; SRY-negative)Pig fatness in relation to FASN and INSIG2 genes polymorphism and their transcript level.Efficient production of multi-modified pigs for xenotransplantation by 'combineering', gene stacking and gene editing.Cytogenetic screening of livestock populations in Europe: an overview.Common polymorphism (81Val>Ile) and rare mutations (257Arg>Ser and 335Ile>Ser) of the MC3R gene in obese Polish children and adolescents.Comparative genomics of 3 farm canids in relation to the dog.Family of melanocortin receptor (MCR) genes in mammals-mutations, polymorphisms and phenotypic effects.A high incidence of adjacent-1 meiotic segregation pattern, revealed by multicolor sperm FISH, in a carrier boar of a new reciprocal translocation t(6;16)(p13;q23).Dog obesity--the need for identifying predisposing genetic markers.Dog as a model in studies on human hereditary diseases and their gene therapy.Transcript level of the porcine ME1 gene is affected by SNP in its 3'UTR, which is also associated with subcutaneous fat thickness.X monosomy in a virilized female cat.Identification of a new reciprocal translocation in an AI bull by synaptonemal complex analysis, followed by chromosome painting.Development of a cytogenetic map for the Chinese raccoon dog (Nyctereutes procyonoides procyonoides) and the arctic fox (Alopex lagopus) genomes, using canine-derived microsatellite probes.Comparative chromosomal localization of the canine-derived BAC clones containing LEP and IGF1 genes in four species of the family Canidae.Two cases of infertile bitches with 78,XX/77,X mosaic karyotype: a need for cytogenetic evaluation of dogs with reproductive disorders.Report on the progress of standardization of the G-banded canine (Canis familiaris) karyotype. Committee for the Standardized Karyotype of the Dog (Canis familiaris).Germline gene polymorphisms predisposing domestic mammals to carcinogenesis.Polymorphism and methylation of the MC4R gene in obese and non-obese dogsGenetics of Adiposity in Large Animal Models for Human Obesity-Studies on Pigs and Dogs.Polymorphisms in the promoter region of the adiponectin (ADIPOQ) gene are presumably associated with transcription level and carcass traits in pigs.Porcine familial adenomatous polyposis model enables systematic analysis of early events in adenoma progression.Molecular evolution of the leptin exon 3 in some species of the family Canidae.The pig CART (cocaine- and amphetamine-regulated transcript) gene and association of its microsatellite polymorphism with production traits.The ACACA and SREBF1 genes are promising markers for pig carcass and performance traits, but not for fatty acid content in the longissimus dorsi muscle and adipose tissue.Altered microRNA profiles during early colon adenoma progression in a porcine model of familial adenomatous polyposis.Confirmation that a deletion in the POMC gene is associated with body weight of Labrador Retriever dogs.Transcript abundance of the pig stearoyl-CoA desaturase gene has no effect on fatty acid composition in muscle and fat tissues, but its polymorphism within the putative microRNA target site is associated with daily body weight gain and feed conversiPolymorphic variants within a putative upstream open reading frame of the MC4R gene do not affect body weight of farmed red foxes.Two candidate genes (FTO and INSIG2) for fat accumulation in four canids: chromosome mapping, gene polymorphisms and association studies of body and skin weight of red foxes.Association of MC3R gene polymorphisms with body weight in the red fox and comparative gene organization in four canids.Variability of CAG tandem repeats in exon 1 of the androgen receptor gene is not related with dog intersexuality.Methylation Patterns of SOX3, SOX9, and WNT4 Genes in Gonads of Dogs with XX (SRY-Negative) Disorder of Sexual Development.
P50
Q27305178-AF738878-CA8F-4586-8D90-51EC90B25B68Q30993144-9D895105-DFBE-4857-94BB-5410BF94501DQ33257111-840C4893-1FF1-4010-9413-21B63DAB50E6Q33300665-D57DEC5C-64A3-4595-9781-4DFD3141DF16Q35093953-3AC258B7-BC24-4908-8792-27CDEAC02221Q35246084-0373397C-B836-4A02-811C-AD8AB65C5A67Q35803830-C07D764A-315F-497D-955F-A26BE4AFC4AEQ36109732-B809BA17-4BA0-4FBC-B561-F5788B8D86A6Q36798952-3BBD8C72-B5C2-440D-8E30-D8F2CADC555BQ37050158-36BF94DA-E854-4F01-9975-66BD58F339BBQ37158349-EB02A551-8027-4349-BBAF-05F34C981E58Q37330731-F5605B3A-FEC6-4D85-9902-C743A80EEBD6Q37656935-C45776B8-9CF0-4DFA-BDFF-32BC1DCBE28AQ38133424-95F2C720-72BA-4CB4-8253-11BD43C8349AQ38136784-5236A86A-E8DB-4475-BCCE-DF3679AFDC72Q38137400-63FB3D56-6B3E-4FDF-85E2-3E6FCBC635CFQ38194317-F01FFB4B-7059-48C0-BF25-8355D766093AQ38310137-E0B7A01A-C640-406D-B98D-06F9CC67A110Q38416664-A43572C7-7D64-4BEC-9B63-3B150CA50176Q38454618-3F589514-E34B-4E29-92A4-8EB6BADFDA52Q38480134-CC328FAC-7A44-42DF-AE60-43C8253A6EE6Q38480141-F1D62DFB-B946-4331-9670-D86CF5B73EC3Q38484500-40FF8912-DE2C-486C-94C2-D7922B42AF4EQ38506931-ECFC6EFA-015E-470C-AC77-27F304AF93CBQ38635393-7A28FDA2-BA5C-41B2-B68F-8DDA0CC19EE6Q38654122-5B1FED24-A8F9-47D3-AFA3-A533CD5B9B90Q38862150-1EDB8370-3117-4E6F-BD1F-E5AB651F82B8Q39311912-9FB04489-A5E4-4C1E-B188-8C40420A90C4Q41140347-60EF9263-CB11-47F3-9535-D7C66AE41AD9Q41396925-5F67FC0F-5BB6-4EBE-B1AA-763B5C6D0499Q44001149-570F79A0-3E4A-4033-90E5-70239124740DQ46136121-EFDA05CB-808E-4C98-96A5-94444A5BB902Q47142174-6CE91A2C-1060-4D63-9021-121EE1E08C80Q47233295-64AF9E2B-4FA2-4E1A-A956-ED433E13AEFDQ47280138-EB42685F-1376-4EFC-9821-178BE22586B2Q47316079-19A69A64-99DA-48F1-A1F9-4EB2DEA6401AQ47360554-ED8CE8C4-C6AF-4588-98D1-0AEC9DAB462BQ47431956-8F4FDAA9-3938-41C1-9FCE-369C829BBDBEQ47688882-E325F9F3-7182-47A4-8816-1A0BEACA63B0Q47807998-5EE3F7DC-CCAF-49A3-8830-60646F28A5F4
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marek Switonski
@ast
Marek Switonski
@en
Marek Switonski
@es
Marek Switonski
@nl
Marek Switonski
@sl
type
label
Marek Switonski
@ast
Marek Switonski
@en
Marek Switonski
@es
Marek Switonski
@nl
Marek Switonski
@sl
prefLabel
Marek Switonski
@ast
Marek Switonski
@en
Marek Switonski
@es
Marek Switonski
@nl
Marek Switonski
@sl
P214
P106
P1153
7005924121
P214
P31
P496
0000-0003-2539-9508
P735
P7859
lccn-n91072596