Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Delf-Magnus Kummerfeld"'
Autor:
Delf-Magnus, Kummerfeld, Boris V, Skryabin, Juergen, Brosius, Sergey Y, Vakhrushev, Timofey S, Rozhdestvensky
Publikováno v:
International journal of molecular sciences. 23(15)
Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by the deletion or inactivation of paternally expressed imprinted genes at the chromosomal region 15q11-q13. The PWS-critical region (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb25c92baf775165058f3dc5e5c24d84
https://pubmed.ncbi.nlm.nih.gov/35955861
https://pubmed.ncbi.nlm.nih.gov/35955861
Autor:
Delf-Magnus Kummerfeld, Boris V. Skryabin, Juergen Brosius, Sergey Y. Vakhrushev, Timofey S. Rozhdestvensky
Publikováno v:
Kummerfeld, D-M, Skryabin, B V, Brosius, J, Vakhrushev, S Y & Rozhdestvensky, T S 2022, ' Reference Genes across Nine Brain Areas of Wild Type and Prader-Willi Syndrome Mice : Assessing Differences in Igfbp7, Pcsk1, Nhlh2 and Nlgn3 Expression ', International Journal of Molecular Sciences, vol. 23, no. 15, 8729 . https://doi.org/10.3390/ijms23158729
International Journal of Molecular Sciences; Volume 23; Issue 15; Pages: 8729
International Journal of Molecular Sciences; Volume 23; Issue 15; Pages: 8729
Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by the deletion or inactivation of paternally expressed imprinted genes at the chromosomal region 15q11–q13. The PWS-critical region (PWScr) harbors tandemly repeated non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c27e6fcf46e1bea17179f2112c6fd478
https://doi.org/10.3390/ijms23158729
https://doi.org/10.3390/ijms23158729
Autor:
Cord Sunderkötter, Roland Wedlich-Söldner, Juergen Brosius, Hermann Pavenstädt, Yuri B. Schwartz, Thomas Pap, Boris V. Skryabin, Sven G. Meuth, Helena Kaiser, Anja Stegemann, Johannes Roth, J. Sherwood, Delf-Magnus Kummerfeld, Timofey S. Rozhdestvensky, Birte Seeger, Leonid Gubar
Publikováno v:
Science Advances
Knock-in genome targeting risks: Comprehensive locus analysis is essential for precision chromosome-editing identification.
CRISPR-Cas9–mediated homology-directed DNA repair is the method of choice for precise gene editing in a wide range of m
CRISPR-Cas9–mediated homology-directed DNA repair is the method of choice for precise gene editing in a wide range of m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f28368132401db8031f263b1847e6a9f
http://europepmc.org/articles/PMC7015686
http://europepmc.org/articles/PMC7015686
Autor:
Reinhard Voss, Delf-Magnus Kummerfeld, Boris V. Skryabin, Jochen Seggewiss, Chenna R. Galiveti, Andreas Huge, Anna Wolters, Carsten A. Raabe, Juergen Brosius, Timofey S. Rozhdestvensky
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Serotonin 5-HT2C receptor is a G-protein coupled excitatory receptor that regulates several biochemical pathways and has been implicated in obesity, mental state, sleep cycles, autism, neuropsychiatric disorders and neurodegenerative diseases. The ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bc90bc012aea307454ecb4162ae5411
http://europepmc.org/articles/PMC6414643
http://europepmc.org/articles/PMC6414643
Autor:
Delf-Magnus Kummerfeld, Raabe, Carsten A, Voss, Reinhard, Juergen Brosius, Chenna R. Galiveti, Wolters, Anna, Seggewiss, Jochen, Huge, Andreas, Skryabin, Boris, Rozhdestvensky, Timofey S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54b919689a23ad4e39c29478316b2178
Autor:
Delf-Magnus Kummerfeld, Timofey S. Rozhdestvensky, Carsten A. Raabe, Dingding Mo, Juergen Brosius, Boris V. Skryabin
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 3613, p 3613 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 3613, p 3613 (2021)
Prader-Willi syndrome (PWS) is a neurogenetic multifactorial disorder caused by the deletion or inactivation of paternally imprinted genes on human chromosome 15q11-q13. The affected homologous locus is on mouse chromosome 7C. The positional conserva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c385dc05555210bd35f3512ddecd24d2
https://doi.org/10.3390/ijms22073613
https://doi.org/10.3390/ijms22073613