Cortes C - Search Results

1

Epithelial Properties of the Second Heart Field.

Cortes C, Francou A, De Bono C, Kelly RG. Cortes C, et al. Circ Res. 2018 Jan 5;122(1):142-154. doi: 10.1161/CIRCRESAHA.117.310838. Circ Res. 2018. PMID: 29301846 Review.

2

T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field.

De Bono C, Thellier C, Bertrand N, Sturny R, Jullian E, Cortes C, Stefanovic S, Zaffran S, Théveniau-Ruissy M, Kelly RG. De Bono C, et al. Among authors: cortes c. Hum Mol Genet. 2018 Nov 1;27(21):3747-3760. doi: 10.1093/hmg/ddy266. Hum Mol Genet. 2018. PMID: 30016433

3

Tbx1 regulates extracellular matrix-cell interactions in the second heart field.

Alfano D, Altomonte A, Cortes C, Bilio M, Kelly RG, Baldini A. Alfano D, et al. Among authors: cortes c. Hum Mol Genet. 2019 Jul 15;28(14):2295-2308. doi: 10.1093/hmg/ddz058. Hum Mol Genet. 2019. PMID: 31180501

4

Protocols for Investigating the Epithelial Properties of Cardiac Progenitor Cells in the Mouse Embryo.

Cortes C, De Bono C, Thellier C, Francou A, Kelly RG. Cortes C, et al. Methods Mol Biol. 2022;2438:231-250. doi: 10.1007/978-1-0716-2035-9_15. Methods Mol Biol. 2022. PMID: 35147946

5

EPySeg: a coding-free solution for automated segmentation of epithelia using deep learning.

Aigouy B, Cortes C, Liu S, Prud'Homme B. Aigouy B, et al. Among authors: cortes c. Development. 2020 Dec 23;147(24):dev194589. doi: 10.1242/dev.194589. Development. 2020. PMID: 33268451 Free PMC article.

6

[No title available]

[No authors listed] [No authors listed] PMID: 34004931

7

Unmasking the ciliopathies: craniofacial defects and the primary cilium.

Cortés CR, Metzis V, Wicking C. Cortés CR, et al. Wiley Interdiscip Rev Dev Biol. 2015 Nov-Dec;4(6):637-53. doi: 10.1002/wdev.199. Epub 2015 Jul 14. Wiley Interdiscip Rev Dev Biol. 2015. PMID: 26173831 Review.

8

Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60.

McInerney-Leo AM, Schmidts M, Cortés CR, Leo PJ, Gener B, Courtney AD, Gardiner B, Harris JA, Lu Y, Marshall M; UK10K Consortium; Scambler PJ, Beales PL, Brown MA, Zankl A, Mitchison HM, Duncan EL, Wicking C. McInerney-Leo AM, et al. Among authors: cortes cr. Am J Hum Genet. 2013 Sep 5;93(3):515-23. doi: 10.1016/j.ajhg.2013.06.022. Epub 2013 Aug 1. Am J Hum Genet. 2013. PMID: 23910462 Free PMC article.

9

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function.

Cortés CR, McInerney-Leo AM, Vogel I, Rondón Galeano MC, Leo PJ, Harris JE, Anderson LK, Keith PA, Brown MA, Ramsing M, Duncan EL, Zankl A, Wicking C. Cortés CR, et al. Sci Rep. 2016 Apr 20;6:24083. doi: 10.1038/srep24083. Sci Rep. 2016. PMID: 27094867 Free PMC article.

10

TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.

Schmidts M, Hou Y, Cortés CR, Mans DA, Huber C, Boldt K, Patel M, van Reeuwijk J, Plaza JM, van Beersum SE, Yap ZM, Letteboer SJ, Taylor SP, Herridge W, Johnson CA, Scambler PJ, Ueffing M, Kayserili H, Krakow D, King SM; UK10K; Beales PL, Al-Gazali L, Wicking C, Cormier-Daire V, Roepman R, Mitchison HM, Witman GB. Schmidts M, et al. Among authors: cortes cr. Nat Commun. 2015 Jun 5;6:7074. doi: 10.1038/ncomms8074. Nat Commun. 2015. PMID: 26044572 Free PMC article.

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