Brenig, Bertram B.

[["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Animal Genetics"],["dc.bibliographiccitation.volume","31"],["dc.contributor.author","Leeb, Tosso"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T09:18:19Z"],["dc.date.available","2018-11-07T09:18:19Z"],["dc.date.issued","2000"],["dc.format.extent","337"],["dc.identifier.doi","10.1046/j.1365-2052.2000.00659.x"],["dc.identifier.isi","000165797800013"],["dc.identifier.pmid","11105220"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28384"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Science Ltd"],["dc.relation.issn","0268-9146"],["dc.title","Two highly polymorphic microsatellites between the canine DAG1 and BSN genes on CFA20q15.1-15.2"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","163"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","KRIMINALISTIK"],["dc.bibliographiccitation.lastpage","164"],["dc.bibliographiccitation.volume","57"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Volkel, I."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T10:40:39Z"],["dc.date.available","2018-11-07T10:40:39Z"],["dc.date.issued","2003"],["dc.identifier.isi","000182109400005"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/46354"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Kriminalistik Verlag"],["dc.relation.issn","0023-4699"],["dc.title","Animals as evidentary organisms - New possibilities in DNA analysis"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","179"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Animal Genetics"],["dc.bibliographiccitation.lastpage","181"],["dc.bibliographiccitation.volume","36"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Voelkel, Inger"],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T11:09:17Z"],["dc.date.available","2018-11-07T11:09:17Z"],["dc.date.issued","2005"],["dc.identifier.doi","10.1111/j.1365-2052.2005.01245.x"],["dc.identifier.isi","000227720000025"],["dc.identifier.pmid","15771741"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/52970"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Publishing Ltd"],["dc.relation.issn","0268-9146"],["dc.title","Phylogenetics of the European Dahomey miniature cattle based on mitochondrial D-loop region DNA sequence"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.subtype","letter_note"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","321"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Animal Genetics"],["dc.bibliographiccitation.lastpage","322"],["dc.bibliographiccitation.volume","30"],["dc.contributor.author","Leeb, T."],["dc.contributor.author","Giese, A."],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Brenig, B."],["dc.date.accessioned","2021-12-08T12:27:32Z"],["dc.date.available","2021-12-08T12:27:32Z"],["dc.date.issued","2001"],["dc.identifier.doi","10.1046/j.1365-2052.1999.00445-5.x"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/95379"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-476"],["dc.relation.issn","0268-9146"],["dc.rights.uri","http://doi.wiley.com/10.1002/tdm_license_1.1"],["dc.title","Two highly polymorphic microsatellites within the porcine ryanodine receptor 3 gene (RYR3)"],["dc.title.alternative","MOLECULAR GENETIC MARKERS"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","55"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Theory in Biosciences"],["dc.bibliographiccitation.lastpage","64"],["dc.bibliographiccitation.volume","124"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Brenig, Bertram"],["dc.contributor.author","Kutschera, U."],["dc.date.accessioned","2018-11-07T08:27:45Z"],["dc.date.available","2018-11-07T08:27:45Z"],["dc.date.issued","2005"],["dc.description.abstract","The phylogenetic relationships of erpobdellid leeches collected throughout Europe were investigated using newly obtained mitochondrial cytochrome c oxidase subunit I (CO-I) gene sequence data from 10 taxa. Monophyly of the five European Erpobdella species (sub-family Erpobdellinae) was supported, but a newly discovered leech, E. wuttkei Kutschera, 2004 (the smallest member of its genus, discovered in an aquarium) was only distantly related to this clade. Three members of the semiaquatic Trochetinae were included in this study. The largest European leech species discovered so far, Trocheta haskonis Grosser, 2000, was found to be a terrestrial predator that feeds on earthworms. The rare species T haskonis is the sister taxon of T bykowskii Gedroye, 1913, a well-known amphibious leech. Based on a comparison of body sizes and a phylogenetic tree the evolution of terrestrialism in the family Erpobdellidae is discussed. (C) 2005 Elsevier GmbH. All rights reserved."],["dc.identifier.doi","10.1016/j.thbio.2005.05.002"],["dc.identifier.isi","000231670300004"],["dc.identifier.pmid","17046348"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/16269"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Urban & Fischer Verlag"],["dc.relation.issn","1431-7613"],["dc.title","Molecular phylogeny of selected predaceous leeches with reference to the evolution of body size and terrestrialism"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","201"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Journal of Animal Breeding and Genetics"],["dc.bibliographiccitation.lastpage","208"],["dc.bibliographiccitation.volume","119"],["dc.contributor.author","Kutzer, T."],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T10:15:59Z"],["dc.date.available","2018-11-07T10:15:59Z"],["dc.date.issued","2002"],["dc.description.abstract","The association between scrapie and polymorphisms of the prion protein (PrP) gene was studied in 1108 German sheep of 33 different breeds. The aim of the investigation was the determination of the codons 136, 154 and 171 of the PrP gene, which are important for scrapie susceptibility. In addition to the published allelic variants ARR, ARQ, AHQ, ARH and VRQ, two novel, rare haplotypes (AHR and VRR) were found in the breeds of Texel, Nolana and Suffolk. A comparison of PrP genotype frequencies among the analysed different breeds revealed distinct variations. Breeds such as Texel showed a complex genotype distribution over 17 variants, while breeds such as Friesian Milk Sheep indicated only seven different genotypes."],["dc.identifier.doi","10.1046/j.1439-0388.2002.00335.x"],["dc.identifier.isi","000177464100001"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/40943"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Verlag Gmbh"],["dc.relation.issn","0931-2668"],["dc.title","Identification of new allelic variants in the ovine prion protein (PrP) gene"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","149"],["dc.bibliographiccitation.issue","2-3"],["dc.bibliographiccitation.journal","Forensic Science International"],["dc.bibliographiccitation.lastpage","151"],["dc.bibliographiccitation.volume","141"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Volkel, I."],["dc.contributor.author","Taubert, H."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T10:48:59Z"],["dc.date.available","2018-11-07T10:48:59Z"],["dc.date.issued","2004"],["dc.description.abstract","The forensic application of DNA-typing for the identification of dog hair provides objective evidence in the characterisation of traces found at crime scenes. During the past few years forensic dog identity testing has been improved considerably using multiplex PCR systems. However, DNA-typing from samples of one up to 10 dog hairs is often problematic in forensic science. A single dog hair contains very small quantities of DNA or the hair sample consists of hairs with roots of bad quality or even of broken hairshafts without roots. Here we describe an experimental study about dog hairs by means of a Ca2+ improved DNA-extraction method, quantification and amplification. (C) 2004 Elsevier Ireland Ltd. All rights reserved."],["dc.identifier.doi","10.1016/j.forsciint.2004.01.016"],["dc.identifier.isi","000220891300013"],["dc.identifier.pmid","15062955"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/48326"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Sci Ireland Ltd"],["dc.relation.issn","0379-0738"],["dc.title","Forensic DNA-typing of dog hair: DNA-extraction and PCR amplification"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","19"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Neurogenetics"],["dc.bibliographiccitation.lastpage","25"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Sander, P."],["dc.contributor.author","Hamann, H."],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Wemheuer, W."],["dc.contributor.author","Brenig, Bertram"],["dc.contributor.author","Groschup, Martin H."],["dc.contributor.author","Ziegler, U."],["dc.contributor.author","Distl, O."],["dc.contributor.author","Leeb, Tosso"],["dc.date.accessioned","2018-11-07T10:51:31Z"],["dc.date.available","2018-11-07T10:51:31Z"],["dc.date.issued","2004"],["dc.description.abstract","Different alleles of the prion protein gene (PRNP) of human and sheep are known to be associated with varying susceptibilities to transmissible spongiform encephalopathies. However, no polymorphisms in the bovine PRNP gene with an effect on susceptibility to prion diseases have been identified to date. In this study we investigated such polymorphisms in German cattle; 48 healthy animals from six different German cattle breeds and 43 cattle with bovine spongiform encephalopathy (BSE) were analyzed. In contrast to previous studies, all three exons as well as the promoter region of the PRNP gene were investigated. Sequence variants in the bovine PRNP gene could have an impact on the amino acid sequence or the expression level of the prion protein and thus on susceptibility to BSE. We identified a total of 60 polymorphisms in the PRNP gene of German cattle. Of these 60 polymorphisms, 36 were newly identified, whereas 24 of these polymorphisms had been described previously. We did not detect any novel polymorphisms affecting the amino acid sequence of the prion protein. However, we identified a 23-bp insertion/deletion polymorphism in the putative PRNP promoter region that shows a significant association with BSE susceptibility in our animals."],["dc.identifier.doi","10.1007/s10048-003-0171-y"],["dc.identifier.isi","000189173500003"],["dc.identifier.pmid","14727152"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/48913"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","1364-6745"],["dc.title","Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","140"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Journal of Animal Breeding and Genetics"],["dc.bibliographiccitation.lastpage","142"],["dc.bibliographiccitation.volume","122"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Brenig, Bertram"],["dc.date.accessioned","2018-11-07T11:11:42Z"],["dc.date.available","2018-11-07T11:11:42Z"],["dc.date.issued","2005"],["dc.description.abstract","Canine leucocyte adhesion deficiency (CLAD) is an autosomal recessive hereditary disease occurring among Irish red setters. The genetic defect causative for this disorder was recently identified as a missense mutation in the ITGB2 gene. Irish red setters with one copy of the mutant gene appear normal, while dogs with two copies of the mutant gene manifest the disease. The present report describes the analysis of the single nucleotide polymorphism in 289 Irish red setters by DNA sequencing. The frequency of CLAD carriers in Germany is 11%."],["dc.identifier.doi","10.1111/j.1439-0388.2005.00500.x"],["dc.identifier.isi","000227593800008"],["dc.identifier.pmid","16130481"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/53493"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Verlag Gmbh"],["dc.relation.issn","0931-2668"],["dc.title","Frequency of the canine leucocyte adhesion deficiency (CLAD) mutation among Irish red setters in Germany"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","47"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Animal Genetics"],["dc.bibliographiccitation.lastpage","50"],["dc.bibliographiccitation.volume","34"],["dc.contributor.author","Brenig, Bertram"],["dc.contributor.author","Pfeiffer, I."],["dc.contributor.author","Jaggy, A."],["dc.contributor.author","Kathmann, I."],["dc.contributor.author","Balzari, M."],["dc.contributor.author","Gaillard, C."],["dc.contributor.author","Dolf, G."],["dc.date.accessioned","2018-11-07T10:41:02Z"],["dc.date.available","2018-11-07T10:41:02Z"],["dc.date.issued","2003"],["dc.description.abstract","The causative mutation in a gene related to hearing loss in Dalmatians has been elusive. Because of its role in melanocyte migration and differentiation as integral component of the inner ear, we hypothesized that the canine PAX3 (paired box homeotic gene 3) gene could be a candidate for Dalmatian deafness. Therefore, we isolated the canine PAX3 gene and searched for causative mutations within the coding region of important regulatory domains of PAX3 . However, no mutations were identified when comparing the DNA sequences of healthy and affected dogs. These results were confirmed by a two-point linkage analysis in 203 Dalmatians transmitting deafness. Our data clearly show that the canine PAX3 gene can be excluded as candidate for Dalmatian deafness."],["dc.identifier.doi","10.1046/j.1365-2052.2003.00931.x"],["dc.identifier.isi","000180800200007"],["dc.identifier.pmid","12580786"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/46447"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Publishing Ltd"],["dc.relation.issn","0268-9146"],["dc.title","Analysis of the 5 ' region of the canine PAX3 gene and exclusion as a candidate for Dalmatian deafness"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]