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| Issue Date | Title | Author(s) |
|---|---|---|
| 11-Sep-2015 | Digenic inheritance in cystinuria mouse model | Espino Gaurch, Meritxell; Font i Llitjós, Mariona; Vilches, Clara; Salido, Eduardo; Prat, Esther; López de Heredia, Miguel; Palacín Prieto, Manuel; Nunes Martínez, Virginia |
| 22-Jan-2018 | Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in Age-Related Hearing Loss. | Espino Gaurch, Meritxell; Font i Llitjós, Mariona; Murillo-Cuesta, Silvia; Errasti-Murugarren, Ekaitz; Celaya, Adelaida M.; Girotto, Giorgia; Vuckovic, Dragana; Mezzavilla, Massimo; Vilches, Clara; Bodoy i Salvans, Susanna; Sahún, Ignasi; González, Laura; Prat, Esther; Zorzano Olarte, Antonio; Dierssen, Mara; Varela-Nieto, Isabel; Gasparini, Paolo; Palacín Prieto, Manuel; Nunes Martínez, Virginia |
| 4-Jun-2019 | Dysfunctional LAT2 amino acid transporter is associated with cataract in mouse and humans | Knöpfel, Emilia Boiadjieva; Vilches, Clara; Camargo, Simone M.; Errasti-Murugarren, Ekaitz; Stäubli, Andrina; Mayayo, Clara; Munier, Francis L.; Miroshnikova, Nataliya; Poncet, Nadège; Junza Martínez, Alexandra; Bhattacharya, Shomi S.; Prat, Esther; Berry, Vanita; Berger, Wolfgang; Heon, Elise; Moore, Anthony T.; Yanes, Oscar; Nunes Martínez, Virginia; Palacín Prieto, Manuel; Verrey, François; Kloeckener-Gruissem, Barbara |
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