Spain (ES)

Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders (2020) Abdelfattah F, Kariminejad A, Kahlert AK, Morrison PJ, Gumus E, Mathews KD, Darbro BW, et al. Journal article FGFR3 Mutation Status and FGFR3 Expression in a Large Bladder Cancer Cohort Treated by Radical Cystectomy: Implications for Anti-FGFR3 Treatment? (2020) van Rhijn BW, Mertens LS, Mayr R, Bostrom PJ, Real FX, Zwarthoff EC, Boormans JL, et al. Journal article Prognostic gene expression signature for high-grade serous ovarian cancer (2020) Millstein J, Budden T, Goode EL, Anglesio MS, Talhouk A, Intermaggio MP, Leong HS, et al. Journal article Monolithic SiC supports with tailored hierarchical porosity for molecularly selective membranes and supported liquid-phase catalysis (2020) Portela R, Marinkovic JM, Logemann M, Schörner M, Zahrtman N, Eray E, Haumann M, et al. Journal article Clinical and pathological associations of PTEN expression in ovarian cancer: a multicentre study from the Ovarian Tumour Tissue Analysis Consortium (2020) Martins FC, Couturier DL, Paterson A, Karnezis AN, Chow C, Nazeran TM, Odunsi A, et al. Journal article Collecting up to 115% of Singlet-Fission Products by Single-Walled Carbon Nanotubes (2020) Menon A, Papadopoulos I, Harreiß C, Mora-Fuentes JP, Cortizo-Lacalle D, Mateo-Alonso A, Spiecker E, Guldi DM Journal article Potassium Poly(Heptazine Imide): Transition Metal-Free Solid-State Triplet Sensitizer in Cascade Energy Transfer and [3+2]-cycloadditions (2020) Savateev A, Tarakina NV, Strauss V, Hussain T, ten Brummelhuis K, Sánchez Vadillo JM, Markushyna Y, et al. Journal article Determinants of Successful Use of Sirolimus in Renal Transplant Patients (2020) Naik MG, Jürgensen JS, Arns W, Basic E, Budde K, Eitner F, Fischereder M, et al. Journal article Low-temperature degradation increases the cyclic fatigue resistance of 3Y-TZP in bending (2020) Belli R, Loher C, Petschelt A, Cicconi MR, de Ligny D, Anglada M, Lohbauer U Journal article De novo mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features (2020) Lehalle D, Vabres P, Sorlin A, Bierhals T, Avila M, Carmignac V, Chevarin M, et al. Journal article