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Browsing by Author Scholl, Francisco G.

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RightsPreviewIssue DateTitleAuthor(s)Type
closedAccessaccesoRestringido.pdf.jpgDec-2015A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic functionTristán Clavijo, E. ; Camacho García, R. J. ; Robles Lanuza, Estefanía ; Ruiz, Agustín; van der Zee, Julie; van Broeckhoven, Christine; Hernández, Isabel; Martínez Mir, Amalia ; Scholl, Francisco G.Artículo
openAccessCharacterization of human PA2.26.pdf.jpg2005Characterization of human PA2.26 antigen (T1α-2, podoplanin), a small membrane mucin induced in oral squamous cell carcinomasMartín-Villar, Ester ; Scholl, Francisco G.; Gamallo, Carlos; Yurrita, María M. ; Muñoz-Guerra, Mario Fernando; Cruces, Jesús ; Quintanilla, Miguel Artículo
closedAccessAug-1995Chronic exposure of cultured transformed mouse epidermal cells to transforming growth factor-beta 1 induces an epithelial-mesenchymal transdifferentiation and a spindle tumoral phenotypeCaulín, Carlos; Scholl, Francisco G.; Frontelo, Pilar; Gamallo, Carlos; Quintanilla, Miguel Artículo
closedAccessaccesoRestringido.pdf.jpgNov-2016Dominant-negative mutation p.Arg324Thr in KCNA1 impairs Kv1.1 channel function in episodic ataxiaTristán Clavijo, E. ; Scholl, Francisco G.; Macaya Ruiz, A.; Iglesias Escalera, G.; Rojas, A. M. ; Lucas, Miguel; Castellano, Antonio; Martínez Mir, Amalia Artículo
closedAccessaccesoRestringido.pdf.jpg2008Dual-promoter lentiviral vectors for constitutive and regulated gene expression in neuronsGascón, Sergio ; Díaz-Guerra, Margarita; Scholl, Francisco G.Artículo
closedAccessaccesoRestringido.pdf.jpg2000Ectopic expression of PA2.26 antigen in epidermal keratinocytes leads to destabilization of adherens junctions and malignant progressionScholl, Francisco G.; Gamallo, Carlos; Quintanilla, Miguel Artículo
closedAccessaccesoRestringido.pdf.jpg1993Expression of intermediate filament proteins by normal and transformed mouse epidermal-keratinocytes in cultureCaulín, Carlos; Gandarillas, Alberto; Scholl, Francisco G.; Quintanilla, Miguel Artículo
closedAccessaccesoRestringido.pdf.jpg2013Genetic study of neurexin and neuroligin genes in Alzheimer's diseaseMartínez Mir, Amalia ; González-Pérez, Antonio; Gayán, Javier; Antúnez, Carmen; Marín, Juan J.; Boada, Mercè; López-Arrieta, Jesús; Fernández, Evaristo; Ramírez Lorca, Reposo; Sáez, María E.; Ruiz, Agustín; Scholl, Francisco G.; Real, Luis MiguelArtículo
closedAccessaccesoRestringido.pdf.jpgNov-2014Genetic study of NRXN1β variants in Spanish patients with schizophreniaAbasolo, Nerea; Roig, Bàrbara; Martorell, Lourdes; Martínez-Leal, R.; Aguilera, Francisco; Camacho García, R. J. ; Orejuela, Carmen; Scholl, Francisco G.; Martínez Mir, Amalia ; Vilella Cuadrada, E.Artículo
closedAccessaccesoRestringido.pdf.jpgSep-2015Identification of causative and susceptibility variants in the neurexin-neuroligin pathway in patients with Alzheimer's disease. The role of a truncating mutation in Neuroligin 1Tristán Clavijo, E. ; Camacho García, R. J. ; Robles Lanuza, Estefanía ; Ruiz, Agustín; Hernández, Isabel; Martínez Mir, Amalia ; Scholl, Francisco G.Póster
openAccessIdentification of PA2.26.pdf.jpgDec-1999Identification of PA2.26 antigen as a novel cell-surface mucin-type glycoprotein that induces plasma membrane extensions and increased motility in keratinocytesScholl, Francisco G.; Gamallo, Carlos; Vilaró, Senén; Quintanilla, Miguel Artículo
closedAccessaccesoRestringido.pdf.jpgOct-2015Mutation p.Arg324Thr in the KCNA1 gene alters Kv1.1 channel function in a family with episodic ataxiaTristán Clavijo, E. ; Scholl, Francisco G.; Iglesias Escalera, G.; Macaya Ruiz, A.; Martínez Mir, Amalia ; Castellano, AntonioPóster
closedAccessaccesoRestringido.pdf.jpg2012Mutations affecting synaptic levels of neurexin-1ß in autism and mental retardationCamacho García, R. J. ; Planelles Fernández, I.; Margalef Estivil, M.; Pecero López, M. L. ; Martínez-Leal, R.; Aguilera, Francisco; Vilella Cuadrada, E.; Martínez Mir, Amalia ; Scholl, Francisco G.Artículo
closedAccessaccesoRestringido.pdf.jpgMar-2013Neurexin and neuroligin genes in Alzheimer's diseaseRuiz, Agustín; Martínez Mir, Amalia ; González-Pérez, Antonio; Gayán, Javier; Antúnez, Carmen; Marín, Juan J.; Boada, Mercè; López-Arrieta, Jesús; Fernández, Evaristo; Ramírez Lorca, Reposo; Sáez, María E.; Scholl, Francisco G.; Real, Luis MiguelPóster
openAccessneurexin_dysfunction_Rabaneda.pdf.jpg24-Jul-2014Neurexin Dysfunction in Adult Neurons Results in Autistic-like Behavior in MiceRabaneda, Luis G. ; Robles Lanuza, Estefanía ; Nieto-González, J.; Scholl, Francisco G.Artículo
openAccess2003PA2.26 antigen (T1α/podoplanin): a small mucin-like transmembrane glycoprotein associated with cell migration and cancerMartín-Villar, Ester ; Scholl, Francisco G.; Gamallo, Carlos; Quintanilla, Miguel Artículo
openAccessPresenilin_saura.pdf.jpg2011Presenilin/Gamma-Secretase Regulates Neurexin Processing at SynapsesSaura, Carlos A.; Servián Morilla, E. ; Scholl, Francisco G.Artículo
closedAccessaccesoRestringido.pdf.jpgDec-2013Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapsesCamacho García, R. J. ; Hervás, Amaia; Toma, Claudio; Balmana, Noemí; Cormand, Bru; Martínez Mir, Amalia ; Scholl, Francisco G.Artículo