Rezultati - Miriam, Fanjul-Fernandez

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  1. 1
    Matrix metalloproteinases: Evolution, gene regulation and functional analysis in mouse models

    Matrix metalloproteinases: Evolution, gene regulation and functional analysis in mouse models od Miriam Fanjul‐Fernández, Alicia R. Folgueras, Sandra Cabrera, Carlos López‐Otín

    Izdano 2009
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  2. 2
    Cell–cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas

    Cell–cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas od Miriam Fanjul‐Fernández, Vı́ctor Quesada, Rubén Cabanillas, Juan Cadiñanos, Tania Fontanil, Álvaro J. Obaya, Andrew Ramsay, José Luís Llorente, Aurora Astudillo, Santiago Cal, Carlos López‐Otín

    Izdano 2013
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  3. 3
    Matrix Metalloproteinase Mmp-1a Is Dispensable for Normal Growth and Fertility in Mice and Promotes Lung Cancer Progression by Modulating Inflammatory Responses

    Matrix Metalloproteinase Mmp-1a Is Dispensable for Normal Growth and Fertility in Mice and Promotes Lung Cancer Progression by Modulating Inflammatory Responses od Miriam Fanjul‐Fernández, Alicia R. Folgueras, Antonio Fueyo, Milagros Balbı́n, María Fernanda Suárez, M. Soledad Fernández-García, Steven D. Shapiro, José M.P. Freije, Carlos López-Otı́n

    Izdano 2013
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  4. 4
    Resistance to Bleomycin-Induced Lung Fibrosis in MMP-8 Deficient Mice Is Mediated by Interleukin-10

    Resistance to Bleomycin-Induced Lung Fibrosis in MMP-8 Deficient Mice Is Mediated by Interleukin-10 od Emilio García-Prieto, Adrián González-López, Sandra Cabrera, Aurora Astudillo, Ana Gutiérrez‐Fernández, Miriam Fanjul‐Fernández, Estefanía Batalla-Solís, Xosé S. Puente, Antonio Fueyo, Carlos López‐Otín, Guillermo M. Albaiceta

    Izdano 2010
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  5. 5
    Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

    Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome od Xosé S. Puente, Vı́ctor Quesada, Fernando G. Osorio, Rubén Cabanillas, Juan Cadiñanos, Julia M. Fraile, Gonzalo R. Ordóñez, Diana Puente, Ana Gutiérrez‐Fernández, Miriam Fanjul‐Fernández, Nicolas Lévy, José M.P. Freije, Carlos López-Otı́n

    Izdano 2011
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  6. 6
    Collagenase-2 Deficiency or Inhibition Impairs Experimental Autoimmune Encephalomyelitis in Mice

    Collagenase-2 Deficiency or Inhibition Impairs Experimental Autoimmune Encephalomyelitis in Mice od Alicia R. Folgueras, Antonio Fueyo, Olivia García‐Suárez, Jennifer H. Cox, Aurora Astudillo, Paolo Tortorella, Cristina Campestre, Ana Gutiérrez‐Fernández, Miriam Fanjul‐Fernández, Caroline J. Pennington, Dylan R. Edwards, Christopher M. Overall, Carlos López-Otı́n

    Izdano 2008
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  7. 7
    A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis

    A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis od Tiong Yang Tan, Sebastian Lunke, Belinda Chong, Dean Phelan, Miriam Fanjul‐Fernández, Justine E. Marum, Vanessa Siva Kumar, Zornitza Stark, Alison Yeung, Natasha J. Brown, Chloe Stutterd, Martin B. Delatycki, Simon Sadedin, Melissa Martyn, Ilias Goranitis, Natalie Thorne, Clara Gaff, Susan M. White

    Izdano 2019
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  8. 8
    Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review

    Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review od Natalie B. Tan, Rachel Stapleton, Zornitza Stark, Martin B. Delatycki, Alison Yeung, Matthew F. Hunter, David J. Amor, Natasha J. Brown, Chloe Stutterd, George McGillivray, Patrick Yap, Matthew Regan, Belinda Chong, Miriam Fanjul‐Fernández, Justine E. Marum, Dean Phelan, Lynn Pais, Susan M. White, Sebastian Lunke, Tiong Yang Tan

    Izdano 2020
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  9. 9
    Meeting the challenges of implementing rapid genomic testing in acute pediatric care

    Meeting the challenges of implementing rapid genomic testing in acute pediatric care od Zornitza Stark, Sebastian Lunke, Gemma R. Brett, Natalie B. Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean Phelan, Belinda Chong, Miriam Fanjul‐Fernández, Justine E. Marum, Matthew F. Hunter, Anna Jarmolowicz, Yael Prawer, Jessica R. Riseley, Matthew Regan, Justine Elliott, Melissa Martyn, Stephanie Best, Tiong Yang Tan, Clara Gaff, Susan M. White

    Izdano 2018
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  10. 10
    Cerebral hypomyelination associated with biallelic variants of FIG4

    Cerebral hypomyelination associated with biallelic variants of FIG4 od Lenk, Guy M., Berry, Ian R., Stutterd, Chloe A., Blyth, Moira, Green, Lydia, Vadlamani, Gayatri, Warren, Daniel, Craven, Ian, Miriam, Fanjul-Fernandez, Victoria, Rodriguez-Casero, Lockhart, Paul J, Vanderver, Adeline, Simons, Cas, Gibb, Susan, Sadedin, Simon, White, Susan M., Christodoulou, John, Skibina, Olga, Ruddle, Jonathan, Tan, Tiong Y., Leventer, Richard J., Livingston, John H., Meisler, Miriam H.

    Izdano 2019
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