Breuss MW - Search Results

1

Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain.

Chung C, Yang X, Hevner RF, Kennedy K, Vong KI, Liu Y, Patel A, Nedunuri R, Barton ST, Noel G, Barrows C, Stanley V, Mittal S, Breuss MW, Schlachetzki JCM, Kingsmore SF, Gleeson JG. Chung C, et al. Among authors: breuss mw. Nature. 2024 May;629(8011):384-392. doi: 10.1038/s41586-024-07292-5. Epub 2024 Apr 10. Nature. 2024. PMID: 38600385 Free PMC article.

2

TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons.

Ngo L, Haas M, Qu Z, Li SS, Zenker J, Teng KS, Gunnersen JM, Breuss M, Habgood M, Keays DA, Heng JI. Ngo L, et al. Hum Mol Genet. 2014 Oct 1;23(19):5147-58. doi: 10.1093/hmg/ddu238. Epub 2014 May 15. Hum Mol Genet. 2014. PMID: 24833723 Free article.

3

Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition.

Breuss MW, Hansen AH, Landler L, Keays DA. Breuss MW, et al. Behav Brain Res. 2017 Apr 14;323:47-55. doi: 10.1016/j.bbr.2017.01.029. Epub 2017 Jan 25. Behav Brain Res. 2017. PMID: 28130172 Free article.

4

Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse.

Edwards A, Treiber CD, Breuss M, Pidsley R, Huang GJ, Cleak J, Oliver PL, Flint J, Keays DA. Edwards A, et al. Neuroscience. 2011 Nov 10;195(4):191-200. doi: 10.1016/j.neuroscience.2011.08.035. Epub 2011 Aug 22. Neuroscience. 2011. PMID: 21875651 Free PMC article.

5

High resolution anatomical mapping confirms the absence of a magnetic sense system in the rostral upper beak of pigeons.

Treiber CD, Salzer M, Breuss M, Ushakova L, Lauwers M, Edelman N, Keays DA. Treiber CD, et al. Commun Integr Biol. 2013 Jul 1;6(4):e24859. doi: 10.4161/cib.24859. Epub 2013 May 10. Commun Integr Biol. 2013. PMID: 23940826 Free PMC article.

6

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

Isrie M, Breuss M, Tian G, Hansen AH, Cristofoli F, Morandell J, Kupchinsky ZA, Sifrim A, Rodriguez-Rodriguez CM, Dapena EP, Doonanco K, Leonard N, Tinsa F, Moortgat S, Ulucan H, Koparir E, Karaca E, Katsanis N, Marton V, Vermeesch JR, Davis EE, Cowan NJ, Keays DA, Van Esch H. Isrie M, et al. Am J Hum Genet. 2015 Dec 3;97(6):790-800. doi: 10.1016/j.ajhg.2015.10.014. Am J Hum Genet. 2015. PMID: 26637975 Free PMC article.

7

The Expression of Tubb2b Undergoes a Developmental Transition in Murine Cortical Neurons.

Breuss M, Morandell J, Nimpf S, Gstrein T, Lauwers M, Hochstoeger T, Braun A, Chan K, Sánchez Guajardo ER, Zhang L, Suplata M, Heinze KG, Elsayad K, Keays DA. Breuss M, et al. J Comp Neurol. 2015 Oct 15;523(15):2161-86. doi: 10.1002/cne.23836. Epub 2015 Aug 11. J Comp Neurol. 2015. PMID: 26105993

8

Microtubules and neurodevelopmental disease: the movers and the makers.

Breuss M, Keays DA. Breuss M, et al. Adv Exp Med Biol. 2014;800:75-96. doi: 10.1007/978-94-007-7687-6_5. Adv Exp Med Biol. 2014. PMID: 24243101 Review.

9

Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly.

Breuss MW, Sultan T, James KN, Rosti RO, Scott E, Musaev D, Furia B, Reis A, Sticht H, Al-Owain M, Alkuraya FS, Reuter MS, Abou Jamra R, Trotta CR, Gleeson JG. Breuss MW, et al. Am J Hum Genet. 2016 Jul 7;99(1):228-35. doi: 10.1016/j.ajhg.2016.05.023. Am J Hum Genet. 2016. PMID: 27392077 Free PMC article.

10

When size matters: CHD8 in autism.

Breuss MW, Gleeson JG. Breuss MW, et al. Nat Neurosci. 2016 Oct 26;19(11):1430-1432. doi: 10.1038/nn.4431. Nat Neurosci. 2016. PMID: 27786184 No abstract available.

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