Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Michaela, Bruntraeger"'
Autor:
Hong Kuang Tan, Shaun K. Y. Goh, Stella Tsotsi, Michaela Bruntraeger, Helen Yu Chen, Birit Broekman, Kok Hian Tan, Yap Seng Chong, Michael J. Meaney, Anqi Qiu, Anne Rifkin-Graboi
Publikováno v:
BMC Psychiatry, Vol 20, Iss 1, Pp 1-14 (2020)
Abstract Background Antenatal maternal anxiety is a risk for offspring psychological and cognitive difficulties. The preschool years represent an important time for brain development, and so may be a window for intervention. However, electrophysiolog
Externí odkaz:
https://doaj.org/article/0e588c576ae745aca666bef3a8d3419c
Autor:
Hugo J. R. Fernandes, Josh P. Kent, Michaela Bruntraeger, Andrew R. Bassett, Albert Koulman, Emmanouil Metzakopian, Stuart G. Snowden
Publikováno v:
Metabolites, Vol 13, Iss 1, p 112 (2023)
The metabolic basis of Parkinson’s disease pathology is poorly understood. However, the involvement of mitochondrial and endoplasmic reticulum stress in dopamine neurons in disease aetiology is well established. We looked at the effect of rotenone-
Externí odkaz:
https://doaj.org/article/fced1bfe2f0945b3af9e3a32bbe49458
All data and analysis files used for the publication "Dynein and dynactin move long-range but are delivered separately to the axon tip"
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::820fa0fe90db436f2d19343a067ee6c9
Autor:
Shaheen Akhtar, Joanna Bottomley, Edward Ryder, Daniel M Barrett, Michaela Bruntraeger, Sanger Mouse Genetics, James Bussell, Jonathan Burvill, Radka Platte, Debarati Sethi, Diane Gleeson
Publikováno v:
Methods (San Diego, Calif.)
Highlights • Next generation sequencing is a scalable solution to genotyping mutant mice. • Ratios of wild type and mutant sequence counts are used to call the genotype. • Hundreds of samples can be multiplexed into one sequencing experiment.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef79b367f901763da5e833510b51bcdc
https://doi.org/10.1016/j.ymeth.2020.10.011
https://doi.org/10.1016/j.ymeth.2020.10.011
Autor:
Nadia Akawi, James Stephenson, Jeffrey C. Barrett, Rebecca E. McIntyre, Hilary C. Martin, Sebastian S. Gerety, Matthew E. Hurles, Carla P. Jones, Diana S. Johnson, John Dean, Sarju G. Mehta, Elena Prigmore, Meena Balasubramanian, Rachel Horton, Michael Wright, Giuseppe Gallone, Mari Niemi, Miranda Splitt, Peter D. Turnpenny, Mark Sanderson, Dhavendra Kumar, Caroline F. Wright, Wendy D Jones, Pradeep C. Vasudevan, Andrew R. Bassett, Juliet Handsaker, Katie Johnson, Joanna Kaplanis, Alice Hulbert, Michaela Bruntraeger, Elizabeth J. Radford, Jenny Morton, Michael J. Parker, Helen V. Firth, Gabriela Sánchez-Andrade, Patrick J. Short, David R. FitzPatrick, Jeremy F. McRae, Sally Ann Lynch
Publikováno v:
2018, ' Quantifying the contribution of recessive coding variation to developmental disorders ', Science . https://doi.org/10.1126/science.aar6731
Genetic architecture of developmental disorders The genetics of developmental disorders (DDs) is complex. Martin et al. wanted to determine the degree of recessive inheritance of DDs in protein-coding genes. They examined the exomes of more than 6000
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d63e07bf84b0aa989d52ad7f110ac3b
https://doi.org/10.1126/science.aar6731
https://doi.org/10.1126/science.aar6731
Akademický článek
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Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1961
Genome editing using the CRISPR/Cas9 system has rapidly established itself as an essential tool in the genetic manipulation of many organisms, including human cell lines. Its application to human induced pluripotent stem cells (hiPSCs) allows for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::14172882ae7c200c141d90734c61e3a0
https://pubmed.ncbi.nlm.nih.gov/30912046
https://pubmed.ncbi.nlm.nih.gov/30912046
Publikováno v:
Methods in Molecular Biology ISBN: 9781493991693
Genome editing using the CRISPR/Cas9 system has rapidly established itself as an essential tool in the genetic manipulation of many organisms, including human cell lines. Its application to human induced pluripotent stem cells (hiPSCs) allows for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12caa1ee7e6e4de4eb1116c03ab9d23a
https://doi.org/10.1007/978-1-4939-9170-9_11
https://doi.org/10.1007/978-1-4939-9170-9_11