Publicaciones
-
Pijuan-Marquilles J, Vilanova-Adell A, Casas-Alba D, Campistol-Plana J, Hoenicka J and Palau F.
Inheritance of c.628-6G>A GNB5 hypomorphic allele uncovers another challenge in the pathogenic prediction of genomic variants
CLINICAL GENETICS . 105(3): 340-342.
-
Pijuan-Marquilles J, Moreno, DF, Yahya, G, Moisa, M, Ul Haq, I, Krukiewicz, K, Mosbah, R, Metwally, K and Cavalu, S.
Regulatory and pathogenic mechanisms in response to iron deficiency and excess in fungi
Microbial Biotechnology . 16(11): 2053-2071. Nº de citas: 5
-
Nascimento-Osorio A, Bruels CC, Donkervoort S, Foley AR, Codina-Bergadà A, Milisenda JC, Estrella EA, Li C, Pijuan-Marquilles J, Draper I, Hu Y, Stafki SA, Pais LS, Ganesh VS, O'Donnell-Luria A, Syeda SB, Carrera-García L, Exposito-Escudero JM, Yubero-Siles D, Martorell-Sampol L, Pinal-Fernandez I, Lidov HGW, Mammen AL, Grau-Junyent JM, Ortez-Gonzalez CI, Palau F, Ghosh PS, Darras BT, Jou-Munoz C, Kunkel LM, Hoenicka J, Bönnemann CG, Kang PB and Natera-de Benito D.
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
ACTA NEUROPATHOLOGICA . 145(4): 479-496. Nº de citas: 2
-
Lopez-Mejia, Isabel C, Pijuan-Marquilles J, Navaridas, Raul, Santacana, Maria, Gatius, Sonia, Velasco, Ana, Castella, Gerard, Panosa, Anais, Cabiscol, Elisa, Pinyol, Miquel, Coll, Laura, Bonifaci, Nuria, Pena, Laura Plata, Vidal, August, Villanueva, Alberto, Gari, Eloi, Llobet-Navas, David, Fajas, Lluis, Matias-Guiu, Xavier and Yeramian, Andree.
Oxidative stress-induced FAK activation contributes to uterine serous carcinoma aggressiveness
MOLECULAR ONCOLOGY . 17(1): 98-118. Nº de citas: 10
-
Pijuan-Marquilles J, Macià A and Panosa A.
Live Cell Adhesion, Migration, and Invasion Assays.
Methods In Molecular Biology (clifton, N.J.) . 2644: 313-329. Nº de citas: 1
-
Martinez-Esteve Melnikova A, Pijuan-Marquilles J, Aparicio J, Ramírez-Camacho A, Altisent A, Vilanova-Adell A, Arzimanoglou A, Armstrong-Moron J, Palau F, Hoenicka J and San Antonio-Arce MV.
The p.Glu787Lys variant in the GRIA3 gene causes developmental and epileptic encephalopathy mimicking structural epilepsy in a female patient.
EUROPEAN JOURNAL OF MEDICAL GENETICS . 65(3): 104442-104442. Nº de citas: 3
-
Pijuan-Marquilles J, Cantarero-Abad L, Natera-de Benito D, Altimir A, Altisent A, Díaz-Osorio Y, Carrera-García L, Exposito-Escudero JM, Ortez-Gonzalez CI, Nascimento-Osorio A, Hoenicka J and Palau F.
Mitochondrial Dynamics and Mitochondria-Lysosome Contacts in Neurogenetic Diseases
FRONTIERS IN NEUROSCIENCE . 16: 784880-784880. Nº de citas: 10
-
Casas-Alba D, Hoenicka J, Vilanova-Adell A, Vega-Hana L, Pijuan-Marquilles J and Palau F.
Diagnostic strategies in patients with undiagnosed and rare diseases
Journal of Translational Genetics and Genomics . 6(3): 322-332. Nº de citas: 2
-
Yahya G, Hashem Mohamed N, Pijuan-Marquilles J, Seleem NM, Mosbah R, Hess S, Abdelmoaty AA, Almeer R, Abdel-Daim MM, Shulaywih Alshaman H, Juraiby I, Metwally K and Storchova Z.
Profiling the physiological pitfalls of anti-hepatitis C direct-acting agents in budding yeast.
Microbial Biotechnology . 14(5): 2199-2213. Nº de citas: 6
-
Pijuan-Marquilles J, Ortigoza-Escobar JD, Juan Jairo Ortiz Guerra, Alcalá-San Martin A, Calvo MJ, Cubells M, Hernando-Davalillo C, Palau F and Hoenicka J.
PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder
AUTISM RESEARCH . 14(6): 1088-1100. Nº de citas: 8