Zobrazeno 1 - 10
of 169
pro vyhledávání: '"J Peter H Burbach"'
Autor:
Tanja C W Nijboer, Ellen V S Hessel, Gijs W van Haaften, Martine J van Zandvoort, Peter J van der Spek, Christine Troelstra, Carolien G F de Kovel, Bobby P C Koeleman, Bert van der Zwaag, Eva H Brilstra, J Peter H Burbach
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0290013 (2023)
Colour agnosia is a disorder that impairs colour knowledge (naming, recognition) despite intact colour perception. Previously, we have identified the first and only-known family with hereditary developmental colour agnosia. The aim of the current stu
Externí odkaz:
https://doaj.org/article/437e002c511c4c28b84eb313bb4302a8
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76037 (2013)
The development of mesodiencephalic dopaminergic (mdDA) neurons located in the substantia nigra compacta (SNc) and ventral tegmental area (VTA) follow a number of stages marked by distinct events. After preparation of the region by signals that provi
Externí odkaz:
https://doaj.org/article/1836f78b39ab47c5910bcd1ade8d58f7
Autor:
Bert van der Zwaag, Lude Franke, Martin Poot, Ron Hochstenbach, Henk A Spierenburg, Jacob A S Vorstman, Emma van Daalen, Maretha V de Jonge, Nienke E Verbeek, Eva H Brilstra, Ruben van 't Slot, Roel A Ophoff, Michael A van Es, Hylke M Blauw, Jan H Veldink, Jacobine E Buizer-Voskamp, Frits A Beemer, Leonard H van den Berg, Cisca Wijmenga, Hans Kristian Ploos van Amstel, Herman van Engeland, J Peter H Burbach, Wouter G Staal
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5324 (2009)
The recent identification of copy-number variation in the human genome has opened up new avenues for the discovery of positional candidate genes underlying complex genetic disorders, especially in the field of psychiatric disease. One major challenge
Externí odkaz:
https://doaj.org/article/115a6726e5774d2e93fc65849cc3a2e9
Autor:
Asami Oguro-Ando, Rosemary A. Bamford, Wiedjai Sital, Jan J. Sprengers, Amila Zuko, Jolien M. Matser, Hugo Oppelaar, Angela Sarabdjitsingh, Marian Joëls, J. Peter. H. Burbach, Martien J. Kas
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Neurodevelopmental and neuropsychiatric disorders, such as autism spectrum disorders (ASD), anorexia nervosa (AN), Alzheimer’s disease (AD), and schizophrenia (SZ), are heterogeneous brain disorders with unknown etiology. Genome wide studi
Externí odkaz:
https://doaj.org/article/53f044de4fd74bb99a68f5ff4e2e7313
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2021)
Autism spectrum disorder (ASD) is characterized by impaired social interaction, language delay and repetitive or restrictive behaviors. With increasing prevalence, ASD is currently estimated to affect 0.5–2.0% of the global population. However, its
Externí odkaz:
https://doaj.org/article/2e7b143b18a74772a295f80a9f0011e5
Autor:
Stanley K. K. Cheung, Jacinda Kwok, Penelope M. Y. Or, Chi Wai Wong, Bo Feng, Kwong Wai Choy, Raymond C. C. Chang, J. Peter H. Burbach, Alfred S. L. Cheng, Andrew M. Chan
Publikováno v:
Scientific Reports. 13
PTEN hamartoma tumour syndrome is characterised by mutations in the human PTEN gene. We performed transcriptomic and proteomic analyses of neural tissues and primary cultures from heterozygous and homozygous Pten-knockout mice. The somatosensory cort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97e461646270c3909fb616d9ad413ace
https://doi.org/10.1038/s41598-023-33869-7
https://doi.org/10.1038/s41598-023-33869-7
Publikováno v:
Biology Open, Vol 4, Iss 8, Pp 954-960 (2015)
Homeodomain transcription factors regulate development of embryos and cellular physiology in adult systems. Paired-type homeodomain genes constitute a subclass that has been particularly implicated in establishment of neuronal identity in the mammali
Externí odkaz:
https://doaj.org/article/ee2b45b8f981404087393cfeeb489978
Autor:
J. Peter H. Burbach, Philip Grant, Anita J. C. G. M. Hellemons, Joseph A. Degiorgis, Ka Wan Li, Harish C. Pant
Publikováno v:
Biology Open, Vol 3, Iss 1, Pp 50-58 (2013)
Summary The giant fiber system of the squid Loligo pealei mediates the escape response and is an important neurobiological model. Here, we identified an abundant transcript in the stellate ganglion (SG) that encodes a FMRFamide precursor, and charact
Externí odkaz:
https://doaj.org/article/69f3acfbe5f74259880abc412250695c
Autor:
Andrew Man-Lok Chan, Stanley Kwok-Kuen Cheung, Jacinda Kwok, Penelope Mei-Yu Or, Chi Wai Wong, Bo Feng, Kwong Wai Choy, Raymond C.C. Chang, J. Peter H. Burbach, Alfred Sze-Lok Cheng
Background: PTEN Hamartoma Tumor Syndrome (PHTS) is characterized by frequent mutation in PTEN gene. PHTS patients have numerous neurological defects including macrocephaly and autism spectrum disorder. While clinical features of PHTS are likely the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::484546bb623c668dd7ca3804d1c1cc1c
https://doi.org/10.21203/rs.3.rs-1575672/v1
https://doi.org/10.21203/rs.3.rs-1575672/v1
Autor:
Jan J. Sprengers, Asami Oguro-Ando, Wiedjai Sital, Marian Joëls, Angela Sarabdjitsingh, Rosemary A. Bamford, J. Peter H. Burbach, Martien J H Kas, Jolien M. Matser, H. Oppelaar, Amila Zuko
Publikováno v:
Translational Psychiatry
Translational Psychiatry, 11(1):106. Nature Publishing Group
Translational Psychiatry, 11, 1, pp. 1-15
Translational Psychiatry, 11, 1-15
Translational Psychiatry, Vol 11, Iss 1, Pp 1-15 (2021)
Translational Psychiatry, 11(1):106. Nature Publishing Group
Translational Psychiatry, 11, 1, pp. 1-15
Translational Psychiatry, 11, 1-15
Translational Psychiatry, Vol 11, Iss 1, Pp 1-15 (2021)
Neurodevelopmental and neuropsychiatric disorders, such as autism spectrum disorders (ASD), anorexia nervosa (AN), Alzheimer’s disease (AD), and schizophrenia (SZ), are heterogeneous brain disorders with unknown etiology. Genome wide studies have r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2ad53fc1febd2b6daac613b6c7d93b
http://europepmc.org/articles/PMC7862349
http://europepmc.org/articles/PMC7862349