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Plos One|February 21, 2012
Structural and functional insights into endoglin ligand recognition and bindingAaron Alt, Laura Miguel-Romero, Jordi Donderis, et al.
Genes & Development|November 5, 2003
The COP1-SPA1 interaction defines a critical step in phytochrome A-mediated regulation of HY5 activityYusuke Saijo, James A Sullivan, Haiyang Wang, et al.
Plos Genetics|September 15, 2010
A central regulatory system largely controls transcriptional activation and repression responses to phosphate starvation in ArabidopsisRegla Bustos, Gabriel Castrillo, Francisco Linhares, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Modular Fluorescent Cholesterol Naphthalimide Probes And Their Application For Cholesterol Trafficking Studies In CellsVicente Rubio, Nicholas McInchak, Genesis Fernandez, et al.
Scientific Reports|December 27, 2024
Development and characterization of fluorescent cholesteryl probes with enhanced solvatochromic and pH-sensitive properties for live-cell imagingVicente Rubio, Nicholas McInchak, Genesis Fernandez, et al.
The Plant Journal : for Cell and Molecular Biology|February 22, 2013
Light and the E3 ubiquitin ligase COP1/SPA control the protein stability of the MYB transcription factors PAP1 and PAP2 involved in anthocyanin accumulation in ArabidopsisAlexander Maier, Andrea Schrader, Leonie Kokkelink, et al.
The FEBS Journal|June 30, 2020
Functional and structural characterization of PII-like protein CutA does not support involvement in heavy metal tolerance and hints at a small-molecule carrying/signaling roleKhaled A Selim, Lorena Tremiño, Clara Marco-Marín, et al.
BMC Veterinary Research|October 12, 2022
Detection of SARS-CoV-2 in a dog with hemorrhagic diarrheaMiguel Padilla-Blanco, Santiago Vega, Luis Enjuanes, et al.
Human Mutation|May 8, 2013
Molecular characterization of carbamoyl-phosphate synthetase (CPS1) deficiency using human recombinant CPS1 as a key toolCarmen Diez-Fernandez, Ana I Martínez, Satu Pekkala, et al.
Journal of Inherited Metabolic Disease|May 13, 2024
Use of pure recombinant human enzymes to assess the disease-causing potential of missense mutations in urea cycle disorders, applied to N-acetylglutamate synthase deficiencyNadine Gougeard, Enea Sancho-Vaello, M Leonor Fernández-Murga, et al.
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