WorldCat Identities

Schütz, Ekkehard

Overview
Works: 15 works in 19 publications in 2 languages and 58 library holdings
Roles: Other, Contributor, dgs, Author
Publication Timeline
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Most widely held works by Ekkehard Schütz
Molekulargenetische Untersuchungen zu Augenerkrankungen beim Holstein Friesian Rind by Anne Katrin Hollmann( )

2 editions published in 2017 in German and held by 14 WorldCat member libraries worldwide

The current study deals with ophthalmological anomalies in Holstein Friesian (HF) cattle and is divided into two parts. The first part of the study considers the development of congenital cataracts in HF cattle. In total 31 cases were examined showing bilateral mature cataracts at time of birth. Pedigree analysis revealed a relationship of all cataract cases indicating an autosomal recessive inheritance of the disorder. A case-control association study based on genotyping data of 26 cases and 88 controls and a subsequent whole genome re-sequencing of one case and four closely related cattle
Identification of molecular genetic causes of bull infertility by Shuwen Shan( )

2 editions published in 2021 in English and held by 4 WorldCat member libraries worldwide

This is a cumulative thesis that includes three different topics around male infertility in cattle and canine diseases. Whole genome association analysis (GWAS) and whole genome sequencing (WGS), as well as additional experimental approaches, were used to identify the candidate genes for these disorders. One of the current challenges facing the dairy industry is to predict and improve the fertility of bulls. We have detected a Holstein bull, who had been approved for artificial insemination based on his semen characteristics, but did not produce offspring after 412 first inseminations, resu
Genetic Analysis of Dog Congenital Deafness and Herding Behavior by Fangzheng Xu( )

2 editions published in 2021 in English and held by 4 WorldCat member libraries worldwide

Strong artificial selections of canine morphological and behavioral traits lead to the formation of more than 400 modern dog (Canis familiaris, CFA) breeds within the past 300 years. Most dog breeds are derived from small numbers of founders, and this closed genetic pool within each breed results in the high frequency of occurrence of canine congenital disorders. The majority of these heredopathies share common clinical signs with corresponding human diseases. Therefore, dogs are appropriate spontaneous models for studying human diseases. Congenital deafness can cause both health and welfar
Association of [alpha]/[beta]-hydrolase D16B with bovine conception rate and sperm plasma membrane lipid composition by Shuwen Shan( )

1 edition published in 2020 in English and held by 3 WorldCat member libraries worldwide

Hämorheologische Wirksamkeit der heparin-induzierten extrakorporalen LDL-Präzipitation (HELP) bei Patienten mit familiärer Hypercholesterinämie by Ekkehard Schütz( Book )

2 editions published between 1988 and 1989 in German and held by 3 WorldCat member libraries worldwide

Osteogenesis imperfecta in a male holstein calf associated with a possible oligogenic origin by Xuying Zhang( )

1 edition published in 2020 in English and held by 3 WorldCat member libraries worldwide

Abstract: Background: Neuromusculoskeletal anomalies generally in combination with severe clinical symptoms, comprise a heterogeneous group of fairly common and mostly fatal disorders in man and animals. Osteogenesis imperfecta (OI), also known as brittle bone disease, causes bone fragility and deformity. Prominent extra-skeletal accessory manifestations of OI comprise blue/gray sclerae, hearing impairment, lung abnormalities and hypercalciuria. Cases of OI in cattle have been reported. However, no causative mutations have been identified in cattle so far.<br><br>Aim: To report a possible oligogenic origin identified in a calf from clinically healthy parents suffering from OI.<br><br>Materials and Methods: A neonatal embryo transfer male Holstein calf developing multiple fractures with bone tissue showing marked osteopenia was used for whole genome re-sequencing as well as its parents. In addition, 2,612 randomly chosen healthy Holstein cattle were genotyped as well as controls.<br><br>Results: Sixteen candidate genes with potential protein-altering variants were selected revealing non-synonymous variants only within IFITM5 and CRTAP genes. However, in-depth gene analysis did not result in the identification of a single causative mutation in the OI calf.<br><br>Conclusion: The analysis of the OI case revealed a possible oligogenic origin of the disease attributable to additive effects of three candidate genes, i.e., ABCA13, QRFPR, and IFTIM5.<br><br>Clinical relevance: Most OI cases in humans and domestic animals reported so far are caused by distinct dominant or recessive monogenic mutations, therefore a potential oligogenic additive genetic effect is a novel finding. Furthermore, the case presented here demonstrates that cross-species genetic analyses might not always be straightforward
Comparative High-Resolution Transcriptome Sequencing of Lymphoma Cell Lines and de novo Lymphomas Reveals Cell-Line-Specific Pathway Dysregulation by Leila Taher( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

Collaborative trial to assess the performance of digital PCR in the field of GMO analysis using an artificial sample material( )

1 edition published in 2017 in English and held by 2 WorldCat member libraries worldwide

DdRADseq reveals determinants for temperature-dependent sex reversal in Nile tilapia on LG23 by Stephan Wessels( )

1 edition published in 2017 in English and held by 2 WorldCat member libraries worldwide

Collaborative trial to assess the performance of digital PCR in the field of GMO analysis using an artificial sample material by René Köppel( )

1 edition published in 2016 in English and held by 2 WorldCat member libraries worldwide

Hoxa9 and Meis1 cooperatively induce addiction to syk signaling by suppressing miR-146a in acute myeloid leukemia by Sebastian Mohr( )

1 edition published in 2017 in English and held by 2 WorldCat member libraries worldwide

Azathioprine Pharmacogenetics: The Relationship between 6-Thioguanine Nucleotides and Thiopurine Methyltransferase in Patients after Heart and Kidney Transplantation by Ekkehard Schütz( )

1 edition published in 1996 in Undetermined and held by 2 WorldCat member libraries worldwide

A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle by Anne K Hollmann( )

1 edition published in 2017 in English and held by 2 WorldCat member libraries worldwide

Die Untersuchung zellfreier DNA durch Liquid Biopsy in der Medizin( )

1 edition published in 2019 in German and held by 2 WorldCat member libraries worldwide

 
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Languages
English (12)

German (6)