Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Deborah S Hartman"'
Autor:
Rebecca Evans, Haruhide Kimura, Masato Nakashima, Takashi Ishikawa, Hiroshi Yukitake, Motohisa Suzuki, James Hazel, Hélène Faessel, Jingtao Wu, Yaming Hang, Robert Alexander, Laura Rosen, Deborah S. Hartman, Emiliangelo Ratti
Publikováno v:
Journal of Sleep Research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b2ee4334095be19c07b3f91f8ebd609
https://doi.org/10.1111/jsr.13878
https://doi.org/10.1111/jsr.13878
Publikováno v:
Advances in Therapy
Introduction Kabuki syndrome is a rare congenital condition characterized clinically by unique facial features, abnormalities in the skeleton, finger pad abnormalities, and developmental delays, as well as a range of other health issues. Existing res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18f344a80dd9d3a07926421e340a0822
http://europepmc.org/articles/PMC8799562
http://europepmc.org/articles/PMC8799562
Autor:
Polyna Khudyakov, Maria S. Quinton, Wei Yin, Saurabh Gupta, Deborah S. Hartman, Dimitrios Arkilo, Jie Lin, Laura Rosen, Jens R. Wendland, Jim Hazel, Martin M. Bednar
Publikováno v:
British Journal of Clinical Pharmacology. 87:4756-4768
Aims Dysregulation of histone methylation epigenetic marks may result in intellectual and developmental disability, as seen in Kabuki syndrome. Animal data suggest that increasing histone methylation by inhibiting lysine-specific demethylase 1A (LSD1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36d95521bc2b88788b5b0a41298167ac
https://doi.org/10.1111/bcp.14912
https://doi.org/10.1111/bcp.14912
Autor:
Rebecca Evans, Haruhide Kimura, Robert Alexander, Ceri H. Davies, Hélène Faessel, Deborah S. Hartman, Takashi Ishikawa, Emiliangelo Ratti, Kohei Shimizu, Motohisa Suzuki, Shinichiro Tanaka, Hiroshi Yukitake, Yves Dauvilliers, Emmanuel Mignot
Publikováno v:
Proceedings of the National Academy of Sciences. 119
Narcolepsy type 1 (NT1) is a sleep disorder caused by a loss of orexinergic neurons. Narcolepsy type 2 (NT2) is heterogeneous; affected individuals typically have normal orexin levels. Following evaluation in mice, the effects of the orexin 2 recepto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2359c6452ab5701e434a27ca5102585
https://doi.org/10.1073/pnas.2207531119
https://doi.org/10.1073/pnas.2207531119
Autor:
Maggie Paulich, Christina Theodore-Oklota, Hans T. Bjornsson, Deborah S. Hartman, Shayna Egan, Deborah Hoffman, Christopher J. Evans
Publikováno v:
American Journal of Medical Genetics. Part a
Publisher's version (útgefin grein)
Kabuki syndrome is a genetic disorder that can affect multiple body systems and manifest as congenital abnormalities and both developmental and socio-emotional delays. The condition is largely unknown by most
Kabuki syndrome is a genetic disorder that can affect multiple body systems and manifest as congenital abnormalities and both developmental and socio-emotional delays. The condition is largely unknown by most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4293dc8334bb01ed3d9793e785bf8098
https://hdl.handle.net/20.500.11815/2311
https://hdl.handle.net/20.500.11815/2311
Publikováno v:
Analytical Biochemistry. 318:91-99
A novel approach to measuring receptor-stimulated phosphoinositide hydrolysis was developed based on the principles of immobilized metal ion affinity chromatography (IMAC) and scintillation proximity assay (SPA). Hard Lewis metal ions, such as Zr(4+)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7202e9d8034f2d95ab390c4fbd51bfd
https://doi.org/10.1016/s0003-2697(03)00159-3
https://doi.org/10.1016/s0003-2697(03)00159-3
Autor:
Deborah S. Hartman, Cornelia Hertel
Publikováno v:
Journal of Neurochemistry. 63:1261-1270
Nerve growth factor (NGF) binds to two distinct cell surface receptors, TrkA, which is a receptor tyrosine kinase, and p75NGFR, whose role in NGF-induced signal transduction remains unclear. We have found that human neuroblastoma IMR-32 cells express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ba5014c2083d1a9016091d188c5582
https://doi.org/10.1046/j.1471-4159.1994.63041261.x
https://doi.org/10.1046/j.1471-4159.1994.63041261.x
Publikováno v:
Journal of Neurochemistry. 68:804-812
The catecholamines dopamine (DA), epinephrine (EP), and norepinephrine (NE) play important roles in learning and memory, emotional states, and control of voluntary movement, as well as cardiovascular and kidney function. They activate distinct but ov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26fff077292bf30ffefddce49e009e17
https://doi.org/10.1046/j.1471-4159.1997.68020804.x
https://doi.org/10.1046/j.1471-4159.1997.68020804.x
Autor:
Dunja Wildt-Perinic, J. Richard L. Pink, Manfred Brockhaus, Fabienne Lanau, Alphonse Probst, Christelle Franchet, Deborah S. Hartman, Corine Goepfert
Publikováno v:
Journal of Neurochemistry. 69:2169-2178
The human dopamine D4 receptor (hD4R), which has been implicated in human diseases such as schizophrenia and in a personality trait called “novelty seeking,” has not yet been characterized at the protein level. Following epitope scanning of the h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c853a25349d185afe35b1894b14c7a
https://doi.org/10.1046/j.1471-4159.1997.69052169.x
https://doi.org/10.1046/j.1471-4159.1997.69052169.x
Autor:
Eric J. Lien, Arima Das, Partha Nandy, Shijun Ren, Horst Kleinkauf, Hans von Döhren, Iradj Hajimohamadreza, J. Mark Treherne, Esteban Domingo, Luis Menéndez-Arias, Miguel E. Quiñones-Mateu, Africa Holguín, Mónica Gutiérrez-Rivas, Miguel A. Martínez, Josep Quer, Isabel S. Novella, John J. Holland, Vijendra K. Singh, Deborah S. Hartman, Olivier Civelli, Vera M. Kolb