Suchergebnisse - Juan Pedro Martı́nez-Barberá
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Molecular and cellular pathogenesis of adamantinomatous craniopharyngioma von Juan Pedro Martı́nez-Barberá
Veröffentlicht 2015Revisão -
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Folic acid prevents exencephaly in Cited2 deficient mice von Juan Pedro Martı́nez-Barberá
Veröffentlicht 2002Artigo -
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Adrenal development is initiated by Cited2 and Wt1 through modulation of Sf-1 dosage von Pierre Val, Juan Pedro Martı́nez-Barberá, Amanda Swain
Veröffentlicht 2007Artigo -
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Cell senescence in neuropathology: A focus on neurodegeneration and tumours von Gabriela Carreno, Romain Guiho, Juan Pedro Martı́nez-Barberá
Veröffentlicht 2020Revisão -
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Paracrine roles of cellular senescence in promoting tumourigenesis von José Mario González-Meljem, John Apps, Helen C. Fraser, Juan Pedro Martı́nez-Barberá
Veröffentlicht 2018Revisão -
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Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development von Carles Gaston‐Massuet, Cynthia L. Andoniadou, Massimo Signore, Ezat Sajedi, Sophie Bird, James M. A. Turner, Juan Pedro Martı́nez-Barberá
Veröffentlicht 2008Artigo -
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Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes von Erwin Pauws, Aya Hoshino, Liz Bentley, Surendra Prajapati, Charles Keller, Peter Hammond, Juan Pedro Martı́nez-Barberá, Gudrun E. Moore, Philip Stanier
Veröffentlicht 2010Artigo -
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Regionalisation of anterior neuroectoderm and its competence in responding to forebrain and midbrain inducing activities depend on mutual antagonism between OTX2 and GBX2 von Juan Pedro Martı́nez-Barberá, Massimo Signore, Pietro Pilo Boyl, Eduardo Puelles, Dario Acampora, Robin Gogoi, F. Schubert, Andrew Lumsden, Antonio Simeone
Veröffentlicht 2001Artigo -
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Galactose‐modified duocarmycin prodrugs as senolytics von Ana Guerrero, Romain Guiho, Nicolás Herranz, Anthony G. Uren, Dominic J. Withers, Juan Pedro Martı́nez-Barberá, Lutz F. Tietze, Jesús Gil
Veröffentlicht 2020Artigo -
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Tbx22 null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes von Erwin Pauws, Aya Hoshino, Lucy Bentley, Suresh I. Prajapati, Charles Keller, Peter Hammond, Juan Pedro Martı́nez-Barberá, Gudrun E. Moore, Philip Stanier
Veröffentlicht 2009Artigo -
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Lack of the murine homeobox gene<i>Hesx1</i>leads to a posterior transformation of the anterior forebrain von Cynthia L. Andoniadou, Massimo Signore, Ezat Sajedi, Carles Gaston‐Massuet, Daniel Kelberman, Alan J. Burns, Nobue Itasaki, Mehul Dattani, Juan Pedro Martı́nez-Barberá
Veröffentlicht 2007Artigo
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Genetics
Gene
Medicine
Cell biology
Endocrinology
Cancer research
Internal medicine
Embryonic stem cell
Phenotype
Transcription factor
Hormone
Receptor
Stem cell
Pathology
Senescence
Signal transduction
Cancer
Embryogenesis
Hypopituitarism
Neuroscience
Paracrine signalling
Pituitary gland
Craniopharyngioma
Embryo
Homeobox
Immunology
Progenitor cell
Wnt signaling pathway
Biochemistry