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A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.
Sci Rep. 2017 Mar 10;7:44138. doi: 10.1038/srep44138.
Sci Rep. 2017.
PMID: 28281571
Free PMC article.
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome.
Urreizti R, Damanti S, Esteve C, Franco-Valls H, Castilla-Vallmanya L, Tonda R, Cormand B, Vilageliu L, Opitz JM, Neri G, Grinberg D, Balcells S.
Urreizti R, et al. Among authors: franco valls h.
Sci Rep. 2018 Jan 12;8(1):694. doi: 10.1038/s41598-017-19109-9.
Sci Rep. 2018.
PMID: 29330474
Free PMC article.
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Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2.
Castilla-Vallmanya L, Centeno-Pla M, Serrano M, Franco-Valls H, Martínez-Cabrera R, Prat-Planas A, Rojano E, Ranea JAG, Seoane P, Oliva C, Paredes-Fuentes AJ, Marfany G, Artuch R, Grinberg D, Rabionet R, Balcells S, Urreizti R.
Castilla-Vallmanya L, et al. Among authors: franco valls h.
J Med Genet. 2023 Apr;60(4):406-415. doi: 10.1136/jmg-2022-108690. Epub 2022 Sep 7.
J Med Genet. 2023.
PMID: 36243518
Free PMC article.
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Abrogation of myofibroblast activities in metastasis and fibrosis by methyltransferase inhibition.
Sala L, Franco-Valls H, Stanisavljevic J, Curto J, Vergés J, Peña R, Duch P, Alcaraz J, García de Herreros A, Baulida J.
Sala L, et al. Among authors: franco valls h.
Int J Cancer. 2019 Dec 1;145(11):3064-3077. doi: 10.1002/ijc.32376. Epub 2019 May 14.
Int J Cancer. 2019.
PMID: 31032902
Free article.
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Formation of an invasion-permissive matrix requires TGFβ/SNAIL1-regulated alternative splicing of fibronectin.
Franco-Valls H, Tusquets-Uxó E, Sala L, Val M, Peña R, Iaconcig A, Villarino Á, Jiménez-Arriola M, Massó P, Trincado JL, Eyras E, Muro AF, Otero J, García de Herreros A, Baulida J.
Franco-Valls H, et al.
Breast Cancer Res. 2023 Nov 14;25(1):143. doi: 10.1186/s13058-023-01736-y.
Breast Cancer Res. 2023.
PMID: 37964360
Free PMC article.
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