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Select item 52900861.

A HETEROZYGOUS MUTATION IN TUBULIN, BETA 2B (TUBB2B) CAUSES COGNITIVE DEFICITS AND HIPPOCAMPAL DISORGANIZATION

Rolf W. Stottmann, Ashley Driver, Arnold Gutierrez, Matthew R. Skelton, Michael Muntifering, Christopher Stepien, Luke Knudson, Matthew Kofron, Charles V. Vorhees, Michael T. Williams

Genes Brain Behav. Author manuscript; available in PMC 2018 Feb 1.

Published in final edited form as: Genes Brain Behav. 2017 Feb; 16(2): 250–259. Published online 2016 Oct 3. doi: 10.1111/gbb.12327

PMCID:: PMC5290086

Abstract Article PDF–1.2M

Select item 28690212.

Tuba8 Is Expressed at Low Levels in the Developing Mouse and Human Brain

Andreas Braun, Martin Breuss, Marion C. Salzer, Jonathan Flint, Nicholas J. Cowan, David A. Keays

Am J Hum Genet. 2010 May 14; 86(5): 819–822. doi: 10.1016/j.ajhg.2010.03.019

PMCID:: PMC2869021

Article PDF–332K

Select item 35956053.

Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

Martin Breuss, Julian Ik-Tsen Heng, Karine Poirier, Guoling Tian, Xavier Hubert Jaglin, Zhengdong Qu, Andreas Braun, Thomas Gstrein, Linh Ngo, Matilda Haas, Nadia Bahi-Buisson, Marie-Laure Moutard, Sandrine Passemard, Alain Verloes, Pierre Gressens, Yunli Xie, Kathryn J.H. Robson, Deepa Selvi Rani, Kumarasamy Thangaraj, Tim Clausen, Jamel Chelly, Nicholas Justin Cowan, David Anthony Keays

Cell Rep. 2012 Dec 27; 2(6): 1554–1562. doi: 10.1016/j.celrep.2012.11.017

PMCID:: PMC3595605

Abstract Article

Select item 37567504.

Postnatal Refinement of Auditory Hair Cell Planar Polarity Deficits Occurs in the Absence of Vangl2

Catherine O. Copley, Jeremy S. Duncan, Chang Liu, Haixia Cheng, Michael R. Deans

J Neurosci. 2013 Aug 28; 33(35): 14001–14016. doi: 10.1523/JNEUROSCI.1307-13.2013

PMCID:: PMC3756750

Abstract Article PDF–5.8M

Select item 66973615.

Differential requirements of tubulin genes in mammalian forebrain development

Elizabeth Bittermann, Zakia Abdelhamed, Ryan P. Liegel, Chelsea Menke, Andrew Timms, David R. Beier, Rolf W. Stottmann

PLoS Genet. 2019 Aug; 15(8): e1008243. Published online 2019 Aug 6. doi: 10.1371/journal.pgen.1008243

PMCID:: PMC6697361

Abstract Article PDF–6.2M

Select item 37816356.

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse

R.W. Stottmann, M. Donlin, A. Hafner, A. Bernard, D.A. Sinclair, D.R. Beier

Hum Mol Genet. 2013 Oct 15; 22(20): 4053–4063. Published online 2013 May 31. doi: 10.1093/hmg/ddt255

PMCID:: PMC3781635

Abstract Article PDF–1.7M

Select item 47287307.

MEKK4 Signaling Regulates Sensory Cell Development and Function in the Mouse Inner Ear

Khujista Haque, Atul K. Pandey, Hong-Wei Zheng, Saima Riazuddin, Su-Hua Sha, Chandrakala Puligilla

J Neurosci. 2016 Jan 27; 36(4): 1347–1361. doi: 10.1523/JNEUROSCI.1853-15.2016

PMCID:: PMC4728730

Abstract Article PDF–4.3M

Select item 31765418.

Focusing Forward Genetics: A Tripartite ENU Screen for Neurodevelopmental Mutations in the Mouse

R. W. Stottmann, J. L. Moran, A. Turbe-Doan, E. Driver, M. Kelley, D. R. Beier

Genetics. 2011 Jul; 188(3): 615–624. doi: 10.1534/genetics.111.126862

PMCID:: PMC3176541

Abstract Article PDF–1.1M

Select item 61554629.

Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration

Alban Latremoliere, Long Cheng, Michelle DeLisle, Chen Wu, Sheena Chew, Elizabeth B. Hutchinson, Andrew Sheridan, Chloe Alexandre, Frederic Latremoliere, Shu-Hsien Sheu, Sara Golidy, Takao Omura, Eric A. Huebner, Yanjie Fan, Mary C. Whitman, Elaine Nguyen, Crystal Hermawan, Carlo Pierpaoli, Max A. Tischfield, Clifford J. Woolf, Elizabeth C. Engle

Cell Rep. Author manuscript; available in PMC 2018 Sep 25.

Published in final edited form as: Cell Rep. 2018 Aug 14; 24(7): 1865–1879.e9. doi: 10.1016/j.celrep.2018.07.029

PMCID:: PMC6155462

Abstract Article PDF–4.9M

Select item 628438710.

TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology

Athanasia Stoupa, Frédéric Adam, Dulanjalee Kariyawasam, Catherine Strassel, Sanjay Gawade, Gabor Szinnai, Alexandre Kauskot, Dominique Lasne, Carsten Janke, Kathiresan Natarajan, Alain Schmitt, Christine Bole‐Feysot, Patrick Nitschke, Juliane Léger, Fabienne Jabot‐Hanin, Frédéric Tores, Anita Michel, Arnold Munnich, Claude Besmond, Raphaël Scharfmann, François Lanza, Delphine Borgel, Michel Polak, Aurore Carré

EMBO Mol Med. 2018 Dec; 10(12): e9569. Published online 2018 Nov 19. doi: 10.15252/emmm.201809569

PMCID:: PMC6284387

Abstract Article PDF–2.4M

Select item 362149311.

Lis1 mediates planar polarity of auditory hair cells through regulation of microtubule organization

Conor W. Sipe, Lixia Liu, Jianyi Lee, Cynthia Grimsley-Myers, Xiaowei Lu

Development. 2013 Apr 15; 140(8): 1785–1795. doi: 10.1242/dev.089763

PMCID:: PMC3621493

Abstract Article

Select item 545714112.

Analogous mechanism regulating formation of neocortical basal radial glia and cerebellar Bergmann glia

Xin Heng, Qiuxia Guo, Alan W Leung, James YH Li

eLife. 2017; 6: e23253. Published online 2017 May 10. doi: 10.7554/eLife.23253

PMCID:: PMC5457141

Abstract Article PDF–11M

Select item 478790313.

The ubiquitin ligase Ubr4 controls stability of podocin/MEC-2 supercomplexes

Markus M. Rinschen, Puneet Bharill, Xiongwu Wu, Priyanka Kohli, Matthäus J. Reinert, Oliver Kretz, Isabel Saez, Bernhard Schermer, Martin Höhne, Malte P. Bartram, Sriram Aravamudhan, Bernard R. Brooks, David Vilchez, Tobias B. Huber, Roman-Ulrich Müller, Marcus Krüger, Thomas Benzing

Hum Mol Genet. 2016 Apr 1; 25(7): 1328–1344. Published online 2016 Jan 19. doi: 10.1093/hmg/ddw016

PMCID:: PMC4787903

Abstract Article PDF–1.0M

Select item 592777114.

Mfn2 ubiquitination by PINK1/parkin gates the p97-dependent release of ER from mitochondria to drive mitophagy

Gian-Luca McLelland, Thomas Goiran, Wei Yi, Geneviève Dorval, Carol X Chen, Nadine D Lauinger, Andrea I Krahn, Sepideh Valimehr, Aleksandar Rakovic, Isabelle Rouiller, Thomas M Durcan, Jean-François Trempe, Edward A Fon

eLife. 2018; 7: e32866. Published online 2018 Apr 20. doi: 10.7554/eLife.32866

PMCID:: PMC5927771

Abstract Article PDF–9.1M

Select item 593680015.

Elucidation of the 14-3-3ζ interactome reveals critical roles of RNA-splicing factors during adipogenesis

Yves Mugabo, Mina Sadeghi, Nancy N. Fang, Thibault Mayor, Gareth E. Lim

J Biol Chem. 2018 May 4; 293(18): 6736–6750. Published online 2018 Mar 12. doi: 10.1074/jbc.M117.816272

PMCID:: PMC5936800

Abstract Article PDF–2.4M

Select item 309339516.

RAD21 Cooperates with Pluripotency Transcription Factors in the Maintenance of Embryonic Stem Cell Identity

Anja Nitzsche, Maciej Paszkowski-Rogacz, Filomena Matarese, Eva M. Janssen-Megens, Nina C. Hubner, Herbert Schulz, Ingrid de Vries, Li Ding, Norbert Huebner, Matthias Mann, Hendrik G. Stunnenberg, Frank Buchholz

PLoS One. 2011; 6(5): e19470. Published online 2011 May 12. doi: 10.1371/journal.pone.0019470

PMCID:: PMC3093395

Abstract Article PDF–1.0M

Select item 655472317.

Interactome Analysis Reveals Regulator of G Protein Signaling 14 (RGS14) is a Novel Calcium/Calmodulin (Ca²⁺/CaM) and CaM Kinase II (CaMKII) Binding Partner

Paul R. Evans, Kyle J. Gerber, Eric B. Dammer, Duc M. Duong, Devrishi Goswami, Daniel J. Lustberg, Juan Zou, Jenny J. Yang, Serena M. Dudek, Patrick R. Griffin, Nicholas T. Seyfried, John R. Hepler

J Proteome Res. Author manuscript; available in PMC 2019 Jun 7.

Published in final edited form as: J Proteome Res. 2018 Apr 6; 17(4): 1700–1711. Published online 2018 Mar 20. doi: 10.1021/acs.jproteome.8b00027

PMCID:: PMC6554723

Abstract Article PDF–2.0M

Select item 634668518.

Plasticity in the Glucagon Interactome Reveals Novel Proteins That Regulate Glucagon Secretion in α-TC1-6 Cells

Farzad Asadi, Savita Dhanvantari

Front Endocrinol (Lausanne) 2018; 9: 792. Published online 2019 Jan 18. doi: 10.3389/fendo.2018.00792

PMCID:: PMC6346685

Abstract Article PDF–3.6M

Select item 586277119.

A CRISPR-based screen for Hedgehog signaling provides insights into ciliary function and ciliopathies

David K. Breslow, Sascha Hoogendoorn, Adam R. Kopp, David W. Morgens, Brandon K. Vu, Margaret C. Kennedy, Kyuho Han, Amy Li, Gaelen T. Hess, Michael C. Bassik, James K. Chen, Maxence V. Nachury

Nat Genet. Author manuscript; available in PMC 2018 Aug 19.

Published in final edited form as: Nat Genet. 2018 Mar; 50(3): 460–471. Published online 2018 Feb 19. doi: 10.1038/s41588-018-0054-7

PMCID:: PMC5862771

Abstract Article PDF–2.5M

Select item 1076935020.

Identification of new ciliary signaling pathways in the brain and insights into neurological disorders

Abdelhalim Loukil, Emma Ebright, Akiyoshi Uezu, Yudong Gao, Scott H Soderling, Sarah C. Goetz

Version 1. bioRxiv. Preprint. 2023 Dec 21. doi: 10.1101/2023.12.20.572700

PMCID:: PMC10769350

Abstract Article PDF–11M

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PMC Links for Gene (Select 73710) (32)
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PREDICTED: Mus musculus serine (or cysteine) peptidase inhibitor, clade B, membe...
PREDICTED: Mus musculus serine (or cysteine) peptidase inhibitor, clade B, member 9c (Serpinb9c), transcript variant X1, mRNA
gi|1720374967|ref|XM_006516618.4|

Nucleotide

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