Arama Sonuçları - Amy E. Pohodich
- Gösterilen 1 - 5 sonuçlar arası kayıtlar. 5
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1
Rett syndrome: disruption of epigenetic control of postnatal neurological functions Yazar: Amy E. Pohodich, Huda Y. Zoghbi
Baskı/Yayın Bilgisi 2015Revisão -
2
Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations Yazar: Ayush T. Raman, Amy E. Pohodich, Ying‐Wooi Wan, Hari Krishna Yalamanchili, William E. Lowry, Huda Y. Zoghbi, Zhandong Liu
Baskı/Yayın Bilgisi 2018Artigo -
3
Forniceal deep brain stimulation induces gene expression and splicing changes that promote neurogenesis and plasticity Yazar: Amy E. Pohodich, Hari Krishna Yalamanchili, Ayush T. Raman, Ying‐Wooi Wan, Michael C. Gundry, Shuang Hao, Haijing Jin, Jianrong Tang, Zhandong Liu, Huda Y. Zoghbi
Baskı/Yayın Bilgisi 2018Artigo -
4
Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders Yazar: Jian Zhou, Hamdan Hamdan, Hari Krishna Yalamanchili, Kaifang Pang, Amy E. Pohodich, Joanna Lopez, Yingyao Shao, Juan A. Osés-Prieto, Lifang Li, Won‐Ho Kim, Mark A. Durham, Sameer S. Bajikar, Donna Palmer, Philip Ng, Michelle L. Thompson, E. Martina Bebin, Amelie J. Müller, Alma Kuechler, Antje Kampmeier, Tobias B. Haack, Alma L. Burlingame, Zhandong Liu, Matthew N. Rasband, Huda Y. Zoghbi
Baskı/Yayın Bilgisi 2022Artigo -
5
Variants in CFAP410 cause a range of retinal and skeletal phenotypes Yazar: Reinhold E. Schmidt, Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung, Nieraj Jain, Michalis Georgiou, Omar A. Mahroo, Andrew R. Webster, Michel Michaelides, Benjamin Bakall, Alessandro Iannaccone, Ajoy Vincent, Deepika C Parameswarappa, Elise Héon, Hendrik P. N. Scholl, Lucas Janeschitz‐Kriegl, Elias I. Traboulsi, Wadih M. Zein, Brian P. Brooks, Catherine A. Cukras, Robert B. Hufnagel, Tomas S. Aleman, Mohamed M. Sylla, Stephen H. Tsang, Michelle Alabek, José‐Alain Sahel, Michael B. Gorin, Maria M. van Genderen, Katarína Štingl, Milda Reith, Susanne Kohl, Rebeca Azevedo Souza Amaral, Juliana Maria Ferraz Sallum, Andrea L. Vincent, Sarah Hull, Jacque L. Duncan, James V. M. Hanson, Matthias Tedeus, Jordi Maggi, U. U. Graf, Samuel Koller, Wolfgang Berger, Christina Gerth‐Kahlert, Molly Marra, Lesley Everett, Paul Yang, Mark E. Pennesi
Baskı/Yayın Bilgisi 2025Artigo
Arama Araçları:
İlgili Konular
Biology
Gene
Genetics
Phenotype
MECP2
Medicine
Neuroscience
Cell biology
Gene expression
Internal medicine
Rett syndrome
Aerospace engineering
Chromatin
Deep brain stimulation
Disease
Encephalopathy
Engineering
Epigenetics
Gene duplication
Intellectual disability
Microarray
Missense mutation
Mutation
Neurodevelopmental disorder
Neurogenesis
Neuroplasticity
Ophthalmology
Parkinson's disease
RNA
RNA splicing