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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2020 | 2 |
2021 | 2 |
2024 | 0 |
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5 results
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Page 1
Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes.
Int J Mol Sci. 2021 Jun 16;22(12):6430. doi: 10.3390/ijms22126430.
Int J Mol Sci. 2021.
PMID: 34208498
Free PMC article.
Knockout of myoc Provides Evidence for the Role of Myocilin in Zebrafish Sex Determination Associated with Wnt Signalling Downregulation.
Atienzar-Aroca R, Aroca-Aguilar JD, Alexandre-Moreno S, Ferre-Fernández JJ, Bonet-Fernández JM, Cabañero-Varela MJ, Escribano J.
Atienzar-Aroca R, et al. Among authors: alexandre moreno s.
Biology (Basel). 2021 Jan 30;10(2):98. doi: 10.3390/biology10020098.
Biology (Basel). 2021.
PMID: 33573230
Free PMC article.
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Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish.
Morales-Cámara S, Alexandre-Moreno S, Bonet-Fernández JM, Atienzar-Aroca R, Aroca-Aguilar JD, Ferre-Fernández JJ, Méndez CD, Morales L, Fernández-Sánchez L, Cuenca N, Coca-Prados M, Martínez-de-la-Casa JM, Garcia-Feijoo J, Escribano J.
Morales-Cámara S, et al. Among authors: alexandre moreno s.
Genes (Basel). 2020 May 14;11(5):550. doi: 10.3390/genes11050550.
Genes (Basel). 2020.
PMID: 32422965
Free PMC article.
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CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix.
Bonet-Fernández JM, Aroca-Aguilar JD, Corton M, Ramírez AI, Alexandre-Moreno S, García-Antón MT, Salazar JJ, Ferre-Fernández JJ, Atienzar-Aroca R, Villaverde C, Iancu I, Tamayo A, Méndez-Hernández CD, Morales-Fernández L, Rojas B, Ayuso C, Coca-Prados M, Martinez-de-la-Casa JM, García-Feijoo J, Escribano J.
Bonet-Fernández JM, et al. Among authors: alexandre moreno s.
Hum Genet. 2020 Oct;139(10):1209-1231. doi: 10.1007/s00439-020-02164-0. Epub 2020 Apr 9.
Hum Genet. 2020.
PMID: 32274568
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Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma.
Medina-Trillo C, Aroca-Aguilar JD, Ferre-Fernández JJ, Alexandre-Moreno S, Morales L, Méndez-Hernández CD, García-Feijoo J, Escribano J.
Medina-Trillo C, et al. Among authors: alexandre moreno s.
PLoS One. 2019 Jan 18;14(1):e0211029. doi: 10.1371/journal.pone.0211029. eCollection 2019.
PLoS One. 2019.
PMID: 30657791
Free PMC article.
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