Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Nico Fuhrmann"'
Publikováno v:
eLife, Vol 12 (2023)
Adaptive ecotype formation can be the first step to speciation, but the genetic underpinnings of this process are poorly understood. Marine midges of the genus Clunio (Diptera) have recolonized Northern European shore areas after the last glaciation.
Externí odkaz:
https://doaj.org/article/4f06ebbb59574f7ab5b77c9343080b89
Autor:
Stephan Holger Drukewitz, Nico Fuhrmann, Eivind A. B. Undheim, Alexander Blanke, Julien Giribaldi, Rosanna Mary, Guillaume Laconde, Sébastien Dutertre, Björn Marcus von Reumont
Publikováno v:
Toxins, Vol 10, Iss 1, p 29 (2018)
Predatory robber flies (Diptera, Asilidae) have been suspected to be venomous due to their ability to overpower well-defended prey. However, details of their venom composition and toxin arsenal remained unknown. Here, we provide a detailed characteri
Externí odkaz:
https://doaj.org/article/846b91b9dcf244bd87fffe2e95cd4b51
Publikováno v:
eLife
Adaptive ecotype formation is the first step to speciation, but the genetic underpinnings of this process are poorly understood. Marine midges of the genus Clunio (Diptera) have recolonized Northern European shore areas after the last glaciation. In
Autor:
Nico Fuhrmann, Tobias S. Kaiser
Publikováno v:
Genome. 64:242-252
DNA barcodes are widely used for species identification and biogeographic studies. Here, we compare the use of full mitochondrial genomes versus DNA barcodes and other mitochondrial DNA fragments for biogeographic and ecological analyses. Our dataset
Autor:
Reza Boostani, Brunhilde Wirth, Sanem Yilmaz, Nico Fuhrmann, Janine Altmueller, Reza Maroofian, Gilbert Wunderlich, Natalie Keller, Olcay Ünver, Bertold Schrank, Cem Paketçi, Uluç Yiş, Susanne Motameny, Peter Nürnberg, Mert Karakaya, Ehsan Ghayoor Karimiani, Holger Thiele
Hereditary lower motor neuron diseases (LMND) other than 5q-spinal muscular atrophy (5q-SMA) can be classified according to affected muscle groups. Proximal and distal forms of non-5q-SMA represent a clinically and genetically heterogeneous spectrum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b937a88cebfcb5475f133c7af13ce71
https://openaccess.sgul.ac.uk/id/eprint/113088/1/humu.24181.pdf
https://openaccess.sgul.ac.uk/id/eprint/113088/1/humu.24181.pdf
Autor:
Brunhilde Wirth, Jonathan Baets, Claudia Gonzaga-Jauregui, Roman Rombo, Stephan Züchner, Nico Fuhrmann, Irmgard Hölker, Maximilian P. Thelen, Vincent J Carson, Peter De Jonghe, Bertold Schrank, Erik G. Puffenberger, Gilbert Wunderlich, Danique Beijer, Kevin A. Strauss, Natalia Mendoza-Ferreira, Mert Karakaya, Nur Cengiz, Tine Deconinck, Sebastian Zetzsche, Karlla W. Brigatti
Publikováno v:
American Journal of Human Genetics
The American Journal of Human Genetics
The American journal of human genetics
The American Journal of Human Genetics
The American journal of human genetics
Distal hereditary motor neuropathies (HMNs) and axonal Charcot-Marie-Tooth neuropathy (CMT2) are clinically and genetically heterogeneous diseases characterized primarily by motor neuron degeneration and distal weakness. The genetic cause for about h
Autor:
Reumont, Stephan Drukewitz, Nico Fuhrmann, Eivind Undheim, Alexander Blanke, Julien Giribaldi, Rosanna Mary, Guillaume Laconde, Sébastien Dutertre, Björn Von
Publikováno v:
Toxins; Volume 10; Issue 1; Pages: 29
Predatory robber flies (Diptera, Asilidae) have been suspected to be venomous due to their ability to overpower well-defended prey. However, details of their venom composition and toxin arsenal remained unknown. Here, we provide a detailed characteri
Autor:
Stephan Holger Drukewitz, Eivind A. B. Undheim, Nico Fuhrmann, Alexander Blanke, Björn M. von Reumont
Publikováno v:
Toxicon. 149:99
Publikováno v:
Human Mutation. 29:106-112
Autosomal dominant optic atrophy (adOA) is most commonly caused by mutations in the OPA1 gene. There is a considerable allelic heterogeneity among adOA-associated OPA1 mutations, however these mutations have mostly been identified and studied only at