Resultats globals: 4 registres trobats en 0.02 segons.
Articles, 4 registres trobats
Articles 4 registres trobats  
1.
20 p, 2.2 MB Obtaining miRNA from Saliva-Comparison of Sampling and Purification Methods / Urbizu, Aintzane (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Arnaldo, Laura (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular) ; Beyer, Katrin (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
The use of saliva as a biomarker source has advantages over other biofluids and imaging techniques, and miRNAs are ideal biomarker candidates. They are involved in numerous cellular processes, and their altered expression suggests that miRNAs play a crucial regulatory role in disease development. [...]
2023 - 10.3390/ijms24032386
International journal of molecular sciences, Vol. 24 (january 2023)  
2.
20 p, 1.3 MB Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1 / Urbizu, Aintzane (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Garrett, Melanie E. (Duke University Medical Center) ; Soldano, Karen (Duke University Medical Center) ; Drechsel, Oliver (Universitat Pompeu Fabra) ; Loth, Dorothy (University of Akron) ; Marcé-Grau, Anna (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Mestres Soler, Olga (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Poca Pastor, María Antonia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Ossowski, Stephan (Universitat Pompeu Fabra) ; Macaya Ruiz, Alfons (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Loth, Francis (University of Akron) ; Labuda, Rick (Conquer Chiari (Estats Units d'Amèrica)) ; Ashley-Koch, Allison (Duke University Medical Center) ; Universitat Autònoma de Barcelona
Chiari Malformation Type 1 (CM-1) is characterized by herniation of the cerebellar tonsils below the foramen magnum and the presence of headaches and other neurologic symptoms. Cranial bone constriction is suspected to be the most common biologic mechanism leading to CM-1. [...]
2021 - 10.1371/journal.pone.0251289
PloS one, Vol. 16 (may 2021)  
3.
15 p, 2.7 MB Expression Levels of an Alpha-Synuclein Transcript in Blood May Distinguish between Early Dementia with Lewy Bodies and Parkinson's Disease / Marsal-García, Laura (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Campdelacreu, Jaume (Hospital Universitari de Bellvitge) ; Vilas, Dolores (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Ispierto, Lourdes (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Gascon-Bayarri, Jordi (Hospital Universitari de Bellvitge) ; Reñé, Ramón (Hospital Universitari de Bellvitge) ; Álvarez, Ramiro (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Beyer, Katrin (Institut Germans Trias i Pujol) ; Urbizu, Aintzane (Institut Germans Trias i Pujol) ; Arnaldo, Laura (Institut Germans Trias i Pujol) ; Universitat Autònoma de Barcelona
Lewy body diseases (LBD) including dementia with Lewy bodies (DLB) and Parkinson disease (PD) are characterized by alpha-synuclein pathology. DLB is difficult to diagnose and peripheral biomarkers are urgently needed. [...]
2021 - 10.3390/ijms22020725
International journal of molecular sciences, Vol. 22 Núm. 2 (2021) , p. 725  
4.
10 p, 379.3 KB Chiari Malformation Type I : a Case-Control Association Study of 58 Developmental Genes / Urbizu, Aintzane (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Toma, Claudio (Universitat de Barcelona. Departament de Genètica) ; Poca Pastor, María Antonia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Sahuquillo Barris, Juan (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Cuenca-León, Ester (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Cormand, Bru (Universitat de Barcelona. Departament de Genètica) ; Macaya Ruiz, Alfons (Hospital Universitari Vall d'Hebron. Institut de Recerca)
Chiari malformation type I (CMI) is a disorder characterized by hindbrain overcrowding into an underdeveloped posterior cranial fossa (PCF), often causing progressive neurological symptoms. The etiology of CMI remains unclear and is most likely multifactorial. [...]
2013 - 10.1371/journal.pone.0057241
PloS one, Vol. 8 Issue 2 (February 2013) , p. e57241  

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1 Urbizu, A.
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