Publicaciones
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Luque J, Mendes I, Gómez B, Morte B, de Heredia ML, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch-Iriberri R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F, CIBERER Network and Lapunzina P.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative
CLINICAL GENETICS . 101(5-6): 481-493. Nº de citas: 8
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López-Marquez A, Morín M, Fernández-Peñalver S, Badosa-Gallego MC, Hernández-Delgado A, Natera-de Benito D, Ortez-Gonzalez CI, Nascimento-Osorio A, Grinberg-Vaisman DR, Balcells S, Roldan-Molina M, Moreno-Pelayo MÁ and Jimenez-Mallebrera C.
CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant COL6A1 Pathogenic Variant Improves Collagen VI Network in Patient Fibroblasts
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 23(8): 4410. Nº de citas: 10
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Martinez-Gil N, Ovejero, D, Garcia-Giralt, N, Bruque, CD, Mellibovsky, L, Nogues, X, Rabionet, R, Grinberg-Vaisman DR and Balcells S.
Genetic Analysis in a Familial Case With High Bone Mineral Density Suggests Additive Effects at Two Loci.
jbmr plus . 6(4): . Nº de citas: 1
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Andrade I, Ribeiro R, Carneiro ZA, Giugliani R, Pereira C, Cozma C, Grinberg-Vaisman DR, Vilageliu L and Lourenco CM.
Fifteen years of enzyme replacement therapy for mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a case report.
Journal Of Medical Case Reports . 16(1): 46-46. Nº de citas: 2
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Garcia-Giralt N, Roca N, Abril JF, Martinez-Gil N, Ovejero D, Castañeda S, Nogues X, Grinberg-Vaisman DR, Balcells S and Rabionet-Janssen R.
Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment.
GENES . 13(1): . Nº de citas: 6
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Martinez-Gil N, Ugartondo N, Grinberg-Vaisman DR and Balcells S.
Wnt Pathway Extracellular Components and Their Essential Roles in Bone Homeostasis.
GENES . 13(1): . Nº de citas: 21
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Beneto N, Grinberg-Vaisman DR, Vilageliu L and Canals I.
Genome Editing Using Cas9-gRNA Ribonucleoprotein in Human Pluripotent Stem Cells for Disease Modeling.
Methods In Molecular Biology (clifton, N.J.) . 2549: 409-425.
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Rauner M, Foessl I, Formosa MM, Kague E, Prijatelj V, Lopez NA, Banerjee B, Bergen D, Busse B, Calado Â, Douni E, Gabet Y, Giralt NG, Grinberg-Vaisman DR, Lovsin NM, Solan XN, Ostanek B, Pavlos NJ, Rivadeneira F, Soldatovic I, van de Peppel J, van der Eerden B, van Hul W, Balcells S, Marc J, Reppe S, Søe K and Karasik D.
Perspective of the GEMSTONE Consortium on Current and Future Approaches to Functional Validation for Skeletal Genetic Disease Using Cellular, Molecular and Animal-Modeling Techniques.
Frontiers in Endocrinology . 12: 731217-731217. Nº de citas: 15
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Martinez-Gil N, Patino, J, Ugartondo, N, Grinberg-Vaisman DR and Balcells S.
WNT16 rs2908004 missense variant acts as eQTL of FAM3C in human primary osteoblasts
Revista de Osteoporosis y Metabolismo Mineral . 13(4): 117-121. Nº de citas: 1
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Cornet-Bartolomé D, Barragán M, Zambelli F, Ferrer-Vaquer A, Tiscornia G, Balcells S, Rodriguez A, Grinberg-Vaisman DR and Vassena R.
Human oocyte meiotic maturation is associated with a specific profile of alternatively spliced transcript isoforms.
MOLECULAR REPRODUCTION AND DEVELOPMENT . 88(9): 605-617. Nº de citas: 6