Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christina Flachmeier"'
Autor:
Benjamin Klein, Tamara Kerscher, Franz Rüschendorf, Christina Flachmeier, Jamina Eckhard, Emmanuel Delaporte, Nick Zimmermann, Theresa Thuß, Claudia Günther, Nicole Berndt, Nadja Lucas, Min Ae Lee-Kirsch, Jorge Esparza-Gordillo, Heiko Traupe, Norbert Hubner, Young-Ae Lee, Ingo Marenholz, Anja Matanovic
Publikováno v:
The Journal of investigative dermatology. 138(6)
Huriez syndrome is a rare dominant genodermatosis characterized by congenital palmoplantar keratosis, scleroatrophic changes of the hands and feet, and an increased risk for cutaneous squamous cell carcinoma (CSCC) in approximately 15% of affected in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90b5f243bb5f868fb6525d3b61230ee
https://pubmed.ncbi.nlm.nih.gov/29409814
https://pubmed.ncbi.nlm.nih.gov/29409814
Autor:
Petra Heere, David Bauer, Siegfried Scherneck, Harald Pankow, Margret R. Hoehe, Wolfgang Schulze, Andreas Hewelt, Christina Flachmeier, Stephan B. Felix, Katrin Wenzel, Ingrid Grunewald
Publikováno v:
Biological Chemistry. 384
We describe the molecular characterization of a novel human gene on chromosome 1q23.3, termed KAT, which is highly conserved among mammals. The KAT gene spans a genomic region of approximately 1.6 kilobases and consists of 4 exons encoding a 115 amin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac61fbbb1b4841a2fcf8162832042889
https://doi.org/10.1515/bc.2003.085
https://doi.org/10.1515/bc.2003.085
Autor:
Hanns Jürgen Kunert, Thomas Rinn, Hannelore Ehrenreich, Karla Köpke, Christina Flachmeier, Petra Heere, Bernd Timmermann, Margret R. Hoehe
Publikováno v:
Europe PubMed Central
Rare but striking individual differences in responsiveness to cannabinoids have been observed that might involve mutations in the gene encoding the brain-expressed cannabinoid receptor. In a preliminary study, the human CB1 cannabinoid receptor codin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f14db9437132275a1133138a3e42bd1
https://pubmed.ncbi.nlm.nih.gov/11324942
https://pubmed.ncbi.nlm.nih.gov/11324942
Autor:
Klaus Rohde, Birgit Wendel, Karla Köpke, George M. Church, Kenneth K. Kidd, Christina Flachmeier, Margret R. Hoehe, Wade H. Berrettini
Publikováno v:
Human molecular genetics. 9(19)
To analyze candidate genes and establish complex genotype-phenotype relationships against a background of high natural genome sequence variability, we have developed approaches to (i) compare candidate gene sequence information in multiple individual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d40aab35137156feeac5df51720f8c7b
https://pubmed.ncbi.nlm.nih.gov/11092766
https://pubmed.ncbi.nlm.nih.gov/11092766