Zobrazeno 1 - 10
of 763
pro vyhledávání: '"Platzer Matthias"'
Autor:
Vos, Stijn, Van den Bergh, Bea R.H., Martens, Dries S., Bijnens, Esmée, Shkedy, Ziv, Kindermans, Hanne, Platzer, Matthias, Schwab, Matthias, Nawrot, Tim S.
Publikováno v:
In Psychoneuroendocrinology September 2024 167
Autor:
Taudien Stefan, Gäbel Gabor, Kuss Oliver, Groth Marco, Grützmann Robert, Huse Klaus, Kluttig Alexander, Wolf Andreas, Nothnagel Michael, Rosenstiel Philip, Greiser Karin Halina, Werdan Karl, Krawczak Michael, Pilarsky Christian, Platzer Matthias
Publikováno v:
BMC Research Notes, Vol 5, Iss 1, p 629 (2012)
Abstract Background Human ß-defensins are a family of antimicrobial peptides located at the mucosal surface. Both sequence multi-site variations (MSV) and copy-number variants (CNV) of the defensin-encoding genes are associated with increased risk f
Externí odkaz:
https://doaj.org/article/138c55bcca3d43f4975a41ec1bea671c
Autor:
Scholz Uwe, Petzold Andreas, Felder Marius, Groth Marco, Schmutzer Thomas, Schulte Daniela, Ariyadasa Ruvini, Steuernagel Burkhard, Taudien Stefan, Mayer Klaus FX, Stein Nils, Platzer Matthias
Publikováno v:
BMC Research Notes, Vol 4, Iss 1, p 411 (2011)
Abstract Background Next generation sequencing of BACs is a viable option for deciphering the sequence of even large and highly repetitive genomes. In order to optimize this strategy, we examined the influence of read length on the quality of Roche/4
Externí odkaz:
https://doaj.org/article/7a60cfdaa0b541619936740f1c005695
Autor:
Zhang Xinmin, Petzold Andreas, Raffaelli Francesca, Huse Klaus, Groth Marco, Felder Marius, Szafranski Karol, Taudien Stefan, Rosenstiel Philip, Hampe Jochen, Schreiber Stefan, Platzer Matthias
Publikováno v:
BMC Genomics, Vol 12, Iss 1, p 243 (2011)
Abstract Background In highly copy number variable (CNV) regions such as the human defensin gene locus, comprehensive assessment of sequence variations is challenging. PCR approaches are practically restricted to tiny fractions, and next-generation s
Externí odkaz:
https://doaj.org/article/0c71d151470e4aa1a2935a01928c5705
Autor:
Kramer Marcel, Boeck Janne, Reichenbach Daniela, Kaether Christoph, Schreiber Stefan, Platzer Matthias, Rosenstiel Philip, Huse Klaus
Publikováno v:
BMC Research Notes, Vol 3, Iss 1, p 224 (2010)
Abstract Background The innate immune system employs several receptor families that form the basis of sensing pathogen-associated molecular patterns. NOD (nucleotide-binding and oligomerization domain) like receptors (NLRs) comprise a group of cytoso
Externí odkaz:
https://doaj.org/article/ce3191667faa4e36ba1d500b0e2a790a
Autor:
Rosenstiel Philip, Hampe Jochen, Szafranski Karol, Petzold Andreas, Huse Klaus, Groth Marco, Taudien Stefan, Schreiber Stefan, Platzer Matthias
Publikováno v:
BMC Genomics, Vol 11, Iss 1, p 252 (2010)
Abstract Background The beta-defensin gene cluster (DEFB) at chromosome 8p23.1 is one of the most copy number (CN) variable regions of the human genome. Whereas individual DEFB CNs have been suggested as independent genetic risk factors for several d
Externí odkaz:
https://doaj.org/article/37ff71ef4a79447dbc84c48625e83dde
Identification and characterization of NAGNAG alternative splicing in the moss Physcomitrella patens
Autor:
Bolte Kathrin, Zimmer Andreas D, Sinha Rileen, Lang Daniel, Reski Ralf, Platzer Matthias, Rensing Stefan A, Backofen Rolf
Publikováno v:
BMC Plant Biology, Vol 10, Iss 1, p 76 (2010)
Abstract Background Alternative splicing (AS) involving tandem acceptors that are separated by three nucleotides (NAGNAG) is an evolutionarily widespread class of AS, which is well studied in Homo sapiens (human) and Mus musculus (mouse). It has also
Externí odkaz:
https://doaj.org/article/369284ee1a974ff2a56ce37b92bf8478
Autor:
Hampe Jochen, Rosenstiel Philip, Huse Klaus, Szafranski Karol, Friedel Swetlana, Gausmann Ulrike, Jahn Niels, Lenser Thorsten, Sinha Rileen, Schuster Stefan, Hiller Michael, Backofen Rolf, Platzer Matthias
Publikováno v:
BMC Bioinformatics, Vol 11, Iss 1, p 216 (2010)
Abstract Background Subtle alternative splicing events involving tandem splice sites separated by a short (2-12 nucleotides) distance are frequent and evolutionarily widespread in eukaryotes, and a major contributor to the complexity of transcriptome
Externí odkaz:
https://doaj.org/article/ef9d35cb7efa4f98bb6a454094490f59
Autor:
Scholz Uwe, Graner Andreas, Felder Marius, Petzold Andreas, Schulte Daniela, Ariyadasa Ruvini, Seidel Michael, Gundlach Heidrun, Taudien Stefan, Steuernagel Burkhard, Mayer Klaus FX, Platzer Matthias, Stein Nils
Publikováno v:
BMC Genomics, Vol 10, Iss 1, p 547 (2009)
Abstract Background De novo sequencing the entire genome of a large complex plant genome like the one of barley (Hordeum vulgare L.) is a major challenge both in terms of experimental feasibility and costs. The emergence and breathtaking progress of
Externí odkaz:
https://doaj.org/article/9c3261936ce34ddfa91677173aceeadb
Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa
Autor:
Herpertz-Dahlmann Beate, Herzog Wolfgang, Scherag André, Nguyen Thuy, Kirschner Jeanette, Brönner Günter, Reichwald Kathrin, Müller Timo, Lichtner Peter, Meitinger Thomas, Platzer Matthias, Schäfer Helmut, Hebebrand Johannes, Hinney Anke
Publikováno v:
Child and Adolescent Psychiatry and Mental Health, Vol 2, Iss 1, p 33 (2008)
Abstract Background Several lines of evidence indicate that the central cannabinoid receptor 1 (CNR1) as well as the major endocannabinoid degrading enzymes fatty acid amide hydrolase (FAAH), N-acylethanolamine-hydrolyzing acid amidase (NAAA) and mon
Externí odkaz:
https://doaj.org/article/30a5062e33cb43cf959990a613d9da44