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Items: 1 to 20 of 56

1.

Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes.

Kasah S, Oddy C, Basson MA.

J Anat. 2018 Dec;233(6):755-769. doi: 10.1111/joa.12889. Epub 2018 Oct 2.

PMID:
30277262
2.

Sex bias in autism: new insights from Chd8 mutant mice?

Andreae LC, Basson MA.

Nat Neurosci. 2018 Sep;21(9):1144-1146. doi: 10.1038/s41593-018-0217-y. No abstract available.

PMID:
30127425
3.

Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.

Suetterlin P, Hurley S, Mohan C, Riegman KLH, Pagani M, Caruso A, Ellegood J, Galbusera A, Crespo-Enriquez I, Michetti C, Yee Y, Ellingford R, Brock O, Delogu A, Francis-West P, Lerch JP, Scattoni ML, Gozzi A, Fernandes C, Basson MA.

Cereb Cortex. 2018 Jun 1;28(6):2192-2206. doi: 10.1093/cercor/bhy058.

4.

Convergence of BMI1 and CHD7 on ERK Signaling in Medulloblastoma.

Badodi S, Dubuc A, Zhang X, Rosser G, Da Cunha Jaeger M, Kameda-Smith MM, Morrissy AS, Guilhamon P, Suetterlin P, Li XN, Guglielmi L, Merve A, Farooq H, Lupien M, Singh SK, Basson MA, Taylor MD, Marino S.

Cell Rep. 2017 Dec 5;21(10):2772-2784. doi: 10.1016/j.celrep.2017.11.021.

5.

Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.

Whittaker DE, Kasah S, Donovan APA, Ellegood J, Riegman KLH, Volk HA, McGonnell I, Lerch JP, Basson MA.

Am J Med Genet C Semin Med Genet. 2017 Dec;175(4). doi: 10.1002/ajmg.c.31595. Epub 2017 Nov 23.

6.

Cerebellar Vermis and Midbrain Hypoplasia Upon Conditional Deletion of Chd7 from the Embryonic Mid-Hindbrain Region.

Donovan APA, Yu T, Ellegood J, Riegman KLH, de Geus C, van Ravenswaaij-Arts C, Fernandes C, Lerch JP, Basson MA.

Front Neuroanat. 2017 Oct 4;11:86. doi: 10.3389/fnana.2017.00086. eCollection 2017.

7.

Engrailed controls epaxial-hypaxial muscle innervation and the establishment of vertebrate three-dimensional mobility.

Ahmed MU, Maurya AK, Cheng L, Jorge EC, Schubert FR, Maire P, Basson MA, Ingham PW, Dietrich S.

Dev Biol. 2017 Oct 1;430(1):90-104. doi: 10.1016/j.ydbio.2017.08.011. Epub 2017 Aug 12.

8.

The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression.

Whittaker DE, Riegman KL, Kasah S, Mohan C, Yu T, Sala BP, Hebaishi H, Caruso A, Marques AC, Michetti C, Smachetti ME, Shah A, Sabbioni M, Kulhanci O, Tee WW, Reinberg D, Scattoni ML, Volk H, McGonnell I, Wardle FC, Fernandes C, Basson MA.

J Clin Invest. 2017 Mar 1;127(3):874-887. doi: 10.1172/JCI83408. Epub 2017 Feb 6.

9.

Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms.

Janecka M, Mill J, Basson MA, Goriely A, Spiers H, Reichenberg A, Schalkwyk L, Fernandes C.

Transl Psychiatry. 2017 Jan 31;7(1):e1019. doi: 10.1038/tp.2016.294. Review.

10.

The neuroanatomy of autism - a developmental perspective.

Donovan AP, Basson MA.

J Anat. 2017 Jan;230(1):4-15. doi: 10.1111/joa.12542. Epub 2016 Sep 12. Review.

11.

An FGFR1-SPRY2 Signaling Axis Limits Basal Cell Proliferation in the Steady-State Airway Epithelium.

Balasooriya GI, Johnson JA, Basson MA, Rawlins EL.

Dev Cell. 2016 Apr 4;37(1):85-97. doi: 10.1016/j.devcel.2016.03.001.

12.

Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome.

Basson MA, van Ravenswaaij-Arts C.

Trends Genet. 2015 Oct;31(10):600-611. doi: 10.1016/j.tig.2015.05.009. Epub 2015 Sep 24. Review.

13.

CHD7 maintains neural stem cell quiescence and prevents premature stem cell depletion in the adult hippocampus.

Jones KM, Sarić N, Russell JP, Andoniadou CL, Scambler PJ, Basson MA.

Stem Cells. 2015 Jan;33(1):196-210. doi: 10.1002/stem.1822.

14.

Epistatic interactions between Chd7 and Fgf8 during cerebellar development: Implications for CHARGE syndrome.

Basson MA.

Rare Dis. 2014 Mar 31;2:e28688. doi: 10.4161/rdis.28688. eCollection 2014.

15.

Endoderm-specific deletion of Tbx1 reveals an FGF-independent role for Tbx1 in pharyngeal apparatus morphogenesis.

Jackson A, Kasah S, Mansour SL, Morrow B, Basson MA.

Dev Dyn. 2014 Sep;243(9):1143-51. doi: 10.1002/dvdy.24147. Epub 2014 Jun 12.

16.

Heparan sulfotransferases Hs6st1 and Hs2st keep Erk in check for mouse corpus callosum development.

Clegg JM, Conway CD, Howe KM, Price DJ, Mason JO, Turnbull JE, Basson MA, Pratt T.

J Neurosci. 2014 Feb 5;34(6):2389-401. doi: 10.1523/JNEUROSCI.3157-13.2014.

17.

Deregulated FGF and homeotic gene expression underlies cerebellar vermis hypoplasia in CHARGE syndrome.

Yu T, Meiners LC, Danielsen K, Wong MT, Bowler T, Reinberg D, Scambler PJ, van Ravenswaaij-Arts CM, Basson MA.

Elife. 2013 Dec 24;2:e01305. doi: 10.7554/eLife.01305.

18.

Coordinated activity of Spry1 and Spry2 is required for normal development of the external genitalia.

Ching ST, Cunha GR, Baskin LS, Basson MA, Klein OD.

Dev Biol. 2014 Feb 1;386(1):1-11. doi: 10.1016/j.ydbio.2013.12.014. Epub 2013 Dec 18.

19.

A bi-modal function of Wnt signalling directs an FGF activity gradient to spatially regulate neuronal differentiation in the midbrain.

Dyer C, Blanc E, Hanisch A, Roehl H, Otto GW, Yu T, Basson MA, Knight R.

Development. 2014 Jan;141(1):63-72. doi: 10.1242/dev.099507. Epub 2013 Nov 27.

20.

Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences.

Basson MA, Wingate RJ.

Front Neuroanat. 2013 Sep 3;7:29. doi: 10.3389/fnana.2013.00029. Review.

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