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1.
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Mol Psychiatry
; 26(11): 6125-6148, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34188164
2.
Tracking population genetic signatures of local extinction with herbarium specimens.
Ann Bot
; 129(7): 857-868, 2022 07 18.
Article
in English
| MEDLINE | ID: mdl-35670810
3.
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development.
Am J Hum Genet
; 101(3): 428-440, 2017 Sep 07.
Article
in English
| MEDLINE | ID: mdl-28823707
4.
Correction: Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Mol Psychiatry
; 26(12): 7852, 2021 Dec.
Article
in English
| MEDLINE | ID: mdl-34282265
5.
Differential patterns of histone methylase EHMT2 and its catalyzed histone modifications H3K9me1 and H3K9me2 during maturation of central auditory system.
Cell Tissue Res
; 365(2): 247-64, 2016 08.
Article
in English
| MEDLINE | ID: mdl-27083448
6.
Dendritic Spine Plasticity: Function and Mechanisms.
Front Synaptic Neurosci
; 12: 36, 2020.
Article
in English
| MEDLINE | ID: mdl-32982715
7.
Single cell RNA sequencing identifies early diversity of sensory neurons forming via bi-potential intermediates.
Nat Commun
; 11(1): 4175, 2020 08 21.
Article
in English
| MEDLINE | ID: mdl-32826903
8.
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis.
Nat Commun
; 10(1): 2129, 2019 05 13.
Article
in English
| MEDLINE | ID: mdl-31086189
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