Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

MyNCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

162 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification.
Young RM, Hawkins TA, Cavodeassi F, Stickney HL, Schwarz Q, Lawrence LM, Wierzbicki C, Cheng BY, Luo J, Ambrosio EM, Klosner A, Sealy IM, Rowell J, Trivedi CA, Bianco IH, Allende ML, Busch-Nentwich EM, Gestri G, Wilson SW. Young RM, et al. Among authors: Wilson SW. Elife. 2019 Feb 19;8:e40093. doi: 10.7554/eLife.40093. Elife. 2019. PMID: 30777146 Free PMC article.
Cell Behaviors during Closure of the Choroid Fissure in the Developing Eye.
Gestri G, Bazin-Lopez N, Scholes C, Wilson SW. Gestri G, et al. Among authors: Wilson SW. Front Cell Neurosci. 2018 Feb 20;12:42. doi: 10.3389/fncel.2018.00042. eCollection 2018. Front Cell Neurosci. 2018. PMID: 29515375 Free PMC article.
The ATPase-dependent chaperoning activity of Hsp90a regulates thick filament formation and integration during skeletal muscle myofibrillogenesis.
Hawkins TA, Haramis AP, Etard C, Prodromou C, Vaughan CK, Ashworth R, Ray S, Behra M, Holder N, Talbot WS, Pearl LH, Strähle U, Wilson SW. Hawkins TA, et al. Among authors: Wilson SW. Development. 2008 Mar;135(6):1147-56. doi: 10.1242/dev.018150. Epub 2008 Feb 6. Development. 2008. PMID: 18256191 Free PMC article.
Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits.
Turner KJ, Hoyle J, Valdivia LE, Cerveny KL, Hart W, Mangoli M, Geisler R, Rees M, Houart C, Poole RJ, Wilson SW, Gestri G. Turner KJ, et al. Among authors: Wilson SW. PLoS One. 2019 Jan 29;14(1):e0211073. doi: 10.1371/journal.pone.0211073. eCollection 2019. PLoS One. 2019. PMID: 30695021 Free PMC article.
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators.
Gestri G, Osborne RJ, Wyatt AW, Gerrelli D, Gribble S, Stewart H, Fryer A, Bunyan DJ, Prescott K, Collin JR, Fitzgerald T, Robinson D, Carter NP, Wilson SW, Ragge NK. Gestri G, et al. Among authors: Wilson SW. Hum Genet. 2009 Dec;126(6):791-803. doi: 10.1007/s00439-009-0730-x. Hum Genet. 2009. PMID: 19685247 Free PMC article.
162 results
Jump to page