Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Tamas Danko"'
Autor:
Bahareh Haddad Derafshi, Tamas Danko, Soham Chanda, Pedro J. Batista, Ulrike Litzenburger, Qian Yi Lee, Yi Han Ng, Anu Sebin, Howard Y. Chang, Thomas C. Südhof, Marius Wernig
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-28 (2022)
Abstract The chromodomain helicase DNA-binding protein CHD8 is the most frequently mutated gene in autism spectrum disorder. Despite its prominent disease involvement, little is known about its molecular function in the human brain. CHD8 is a chromat
Externí odkaz:
https://doaj.org/article/f6144c8eb12747dd9d2726213f094bb0
Autor:
Pedro J. Batista, Bahareh Haddad Derafshi, Tamas Danko, Marius Wernig, Thomas C. Südhof, Yi Han Ng, Ulrike Litzenburger, Anu Sebin, Soham Chanda, Howard Y. Chang, Qian Yi Lee
Publikováno v:
Scientific Reports. 12
The chromodomain helicase DNA-binding protein CHD8 is among the most frequently found de-novo mutations in autism (1–3). Unlike most other autism-risk genes, CHD8 mutations appear to be fully penetrant (4). Despite its prominent disease involvement
Autor:
Alexis Mitelpunkt, Koji Tanabe, Anshul Kundaje, Wing Hung Wong, Cheen Euong Ang, Jonathan A. Bernstein, Tamas Danko, Soumya Kundu, Bruce J. Aronow, Joachim Hallmayer, Carolin Purmann, Alexander E. Urban, Shining Ma, Thomas C. Südhof, Yue Zhang, Marius Wernig
Standard methods for the creation of neuronal cells via direct induction from primary tissue use perinatal fibroblasts, which hinders the important study of patient specific genetic lesions such as those underlying neuropsychiatric disorders. To addr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ac794fc56f488fdc1f69e3270cabe91
https://doi.org/10.1101/2021.10.14.464344
https://doi.org/10.1101/2021.10.14.464344
Autor:
Philip Dexheimer, Jeffrey L. Dage, Xianglong Zhang, Thomas J. Ward, Yu-Wen Alvin Huang, Yingfei Liu, Marius Wernig, Zhiping P. Pang, Tamas Danko, ChangHui Pak, Jinzhao Wang, Vincent R. Mirabella, Kang Jin, Michael McLachlan, Madhuri Vangipuram, Carolin Purmann, Jennifer C. Moore, Junyi Ma, Bradley J. Swanson, Sarah Grieder, Eric E. Bardes, Douglas F. Levinson, Alexis Mitelpunkt, Bruce J. Aronow, Alexander E. Urban, Thomas C. Südhof, Pingping Qu
Publikováno v:
Proc Natl Acad Sci U S A
Heterozygous NRXN1 deletions constitute the most prevalent currently known single-gene mutation predisposing to schizophrenia. Previous studies showed that engineered heterozygous NRXN1 deletions impaired neurotransmitter release in human neurons, su
Autor:
Katalin Horvath, Beáta Zs. Kovács, Tamas Danko, Ildikó Somlyai, Gábor Somlyai, Miklos Z. Molnar
Publikováno v:
Molecular and Cellular Biochemistry
BackgroundDeuterium (D) is a stable isotope of hydrogen (H) with a mass number of 2. It is present in natural waters in the form of HDO, at a concentration of 16.8 mmol/L, equivalent to 150 ppm. In a phase II clinical study, deuterium depletion reduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f26a7652a5e752919d55aebc0561251
https://doi.org/10.21203/rs.3.rs-117904/v1
https://doi.org/10.21203/rs.3.rs-117904/v1
Autor:
Fei Yi, Jason Aoto, Garret R. Anderson, Stephan Maxeiner, Thomas C. Südhof, Yingsha Zhang, Tamas Danko, Marius Wernig, ChangHui Pak
Publikováno v:
Cell stem cell, vol 17, iss 3
Heterozygous mutations of the NRXN1 gene, which encodes the presynaptic cell-adhesion molecule neurexin-1, were repeatedly associated with autism and schizophrenia. However, diverse clinical presentations of NRXN1 mutations in patients raise the ques
Autor:
Matthias A. Hediger, Ákos Zsembery, Gergely Kovacs, Bernadett Balázs, Tamas Danko, László Köles
Publikováno v:
Cellular Physiology and Biochemistry, Vol 32, Iss 1, Pp 11-24 (2013)
Balázs, B.; Dankó, T.; Kovács, G.; Köles, L.; Hediger, M. A.; Zsembery, Á. (2013). Investigation of the inhibitory effects of the benzodiazepine derivative, 5-BDBD on P2X4 purinergic receptors by two complementary methods. Cellular physiology and biochemistry, 32(1), pp. 11-24. Karger 10.1159/000350119
Balázs, B.; Dankó, T.; Kovács, G.; Köles, L.; Hediger, M. A.; Zsembery, Á. (2013). Investigation of the inhibitory effects of the benzodiazepine derivative, 5-BDBD on P2X4 purinergic receptors by two complementary methods. Cellular physiology and biochemistry, 32(1), pp. 11-24. Karger 10.1159/000350119
BACKGROUND/AIMS ATP-gated P2X4 purinergic receptors (P2X4Rs) are cation channels with important roles in diverse cell types. To date, lack of specific inhibitors has hampered investigations on P2X4Rs. Recently, the benzodiazepine derivative, 5-BDBD h
Autor:
Jason P. Covy, Soham Chanda, Yingsha Zhang, Thomas C. Südhof, ChangHui Pak, Lu Chen, Nan Yang, Claudio Acuna, Wei Xu, Christopher Patzke, Henrik Ahlenius, Tamas Danko, Zhenjie Zhang, Samuele Marro, Marius Wernig, Yan Han
Publikováno v:
Neuron. 78(5):785-798
SummaryAvailable methods for differentiating human embryonic stem cells (ESCs) and induced pluripotent cells (iPSCs) into neurons are often cumbersome, slow, and variable. Alternatively, human fibroblasts can be directly converted into induced neuron
Autor:
Tamas Danko, Nicolas Montalbetti, Ákos Zsembery, Matthias A. Hediger, Gergely Kovacs, Alexandre Simonin, Bernadett Balázs
Publikováno v:
Cell Calcium. 52:468-480
TRPV6, a highly calcium-selective member of the transient receptor potential (TRP) channel superfamily, is a major pathway for calcium absorption in the fetal and adult body. It is expressed abundantly in the duodenum, the placenta and exocrine tissu
Autor:
Fei Yi, Tamas Danko, Marius Wernig, Christopher Patzke, ChangHui Pak, Thomas C. Südhof, Salomé Calado Botelho
Publikováno v:
Science. 352
Faulty channels, not faulty synapses SHANK3 is a widely expressed scaffolding protein that is enriched in postsynaptic specializations. In mutant mice, SHANK3 mutations cause autism-like behavioral changes and exhibit alterations in synaptic transmis