Deppe, Arvid Sönke

[["dc.bibliographiccitation.firstpage","335"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Animal Genetics"],["dc.bibliographiccitation.lastpage","336"],["dc.bibliographiccitation.volume","31"],["dc.contributor.author","Leeb, Tosso"],["dc.contributor.author","Deppe, A."],["dc.contributor.author","Kriegesmann, B."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T09:17:52Z"],["dc.date.available","2018-11-07T09:17:52Z"],["dc.date.issued","2000"],["dc.identifier.doi","10.1046/j.1365-2052.2000.00656.x"],["dc.identifier.isi","000165797800011"],["dc.identifier.pmid","11105218"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28272"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Science Ltd"],["dc.relation.issn","0268-9146"],["dc.title","Genomic structure and nucleotide polymorphisms of the porcine agouti signalling protein gene (ASIP)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","295"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Genome Research"],["dc.bibliographiccitation.lastpage","301"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Leeb, Tosso"],["dc.contributor.author","Neumann, S."],["dc.contributor.author","Deppe, A."],["dc.contributor.author","Breen, M."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T09:10:18Z"],["dc.date.available","2018-11-07T09:10:18Z"],["dc.date.issued","2000"],["dc.description.abstract","Dystroglycan is a laminin binding protein, which provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix. It is also involved in the organization of basement membranes. So far the genomic organization of the dystroglycan gene DAG1 has nor been completely investigated. Here we report the cloning and sequencing of 162 kb of dog genomic DNA containing the complete similar to 71-kb canine DAG1 gene, which consists of three exons, with the translation start codon located in exon 2. Its 2679-nucleotide ORF encodes a polypeptide of 892 amino acids, which is highly similar to human, rabbit, and bovine orthologs. To further characterize the dog DAG1 gene we determined,the transcription start site and several naturally occurring polymorphisms, which partially result in amino acid substitutions of the dystroglycan protein. The dog DAG1 gene was assigned to chromosome 20q15.1-q15.2 by FISH analysis. The analysis of the entire reported sequence revealed that the genes for aminomethyltransferase (AMT), bassoon (BSN), TCTA (T-cell leukemia translocation-associated) gene, and an as yet uncharacterized protein are located very close to the DAG1 gene. Therefore, this study defines a novel syntenic region among dog chromosome 20q15, human chromosome 3p21, and murine chromosome 9F."],["dc.identifier.doi","10.1101/gr.10.3.295"],["dc.identifier.isi","000085868500004"],["dc.identifier.pmid","10720570"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/26457"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Cold Spring Harbor Lab Press"],["dc.relation.issn","1088-9051"],["dc.title","Genomic organization of the dog dystroglycan gene DAG1 locus on chromosome 20q15.1-q15.2"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","186"],["dc.bibliographiccitation.issue","3-4"],["dc.bibliographiccitation.journal","CYTOGENETICS AND CELL GENETICS"],["dc.bibliographiccitation.lastpage","189"],["dc.bibliographiccitation.volume","94"],["dc.contributor.author","Conrad, K."],["dc.contributor.author","Deppe, A."],["dc.contributor.author","Neumann, S."],["dc.contributor.author","Breen, M."],["dc.contributor.author","Quignon, P."],["dc.contributor.author","Andre, C."],["dc.contributor.author","Brenig, Bertram"],["dc.contributor.author","Leeb, Tosso"],["dc.date.accessioned","2018-11-07T09:31:02Z"],["dc.date.available","2018-11-07T09:31:02Z"],["dc.date.issued","2001"],["dc.description.abstract","Mutations in the gene for gamma-sarcoglycan (SGCG) located on HSA 13q12 are responsible for limb girdle muscular dystrophy (LGMD2C) in human. Here we report the cloning of the canine SGCG gene together with its genomic structure and several intragenic polymorphisms. The coding part of the canine SGCG contains seven exons spanning at least 70 kb of genomic DNA. The chromosome assignment of the canine SGCG gene to CFA 25q21 --> q23 confirms that the canine syntenic group 10 corresponds to CFA 2 5 and also supports the findings of human-canine reciprocal chromosome painting. Copyright (C) 2002 S. Karger AG, Basel."],["dc.identifier.doi","10.1159/000048813"],["dc.identifier.isi","000174156400015"],["dc.identifier.pmid","11856878"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/31449"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Karger"],["dc.relation.issn","0301-0171"],["dc.title","Characterization and chromosome assignment of the canine gamma-sarcoglycan gene (SGCG) to CFA 25q21 -> q23"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","175"],["dc.bibliographiccitation.issue","1-2"],["dc.bibliographiccitation.journal","DNA SEQUENCE"],["dc.bibliographiccitation.lastpage","179"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Giese, A."],["dc.contributor.author","Deppe, A."],["dc.contributor.author","Brenig, Bertram"],["dc.contributor.author","Leeb, Tosso"],["dc.date.accessioned","2018-11-07T11:03:35Z"],["dc.date.available","2018-11-07T11:03:35Z"],["dc.date.issued","2000"],["dc.description.abstract","Ryanodine receptor 3 is a calcium channel located in the membrane of the endoplasmic reticulum. We isolated eight overlapping PAC clones from the porcine ryanodine receptor 3 gene (RYR3) and determined the DNA sequences of the first and second exon together with 5.8 kb of 5' flanking region and 10.3 kb of intron sequences. By comparing the porcine genomic sequence to the human RYR3 cDNA sequence the porcine transcription start site could be mapped to a GC-rich region. Physical mapping of the isolated PAC clones revealed that the complete porcine RYR3 gene spans more than 200 kb of genomic DNA."],["dc.identifier.isi","000088802700024"],["dc.identifier.pmid","10902927"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/51655"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Harwood Acad Publ Gmbh"],["dc.relation.issn","1042-5179"],["dc.title","Genomic structure of the 5 ' end of the porcine ryanodine receptor 3 gene (RYR3)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]