Visualitzant R - Articles científics per títol

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Gracia-Diaz, Carolina; Zhou, Yijing; Yang, Qian; Maroofian, Reza; España, Paula; Lee, Chul-Hwan; Padilla Sirera, Natàlia (Nature Portfolio, 2023-07-11)

Gait analysis under the lens of statistical physics

Zanin, Massimiliano; Olivares, Felipe; Pulido-Valdeolivas, Irene; Rausell Tamayo, Estrella; Gómez Andrés, David (Elsevier, 2022)

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis

Pozo Rosich, Patricia; Samaan, Karen; Schwedt, Todd J.; Nicholson, Robert A.; Rettiganti, Mallikarjuna; Pearlman, Eric M. (Springer, 2021-06)

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells

Bellio, Chiara; Emperador, Marta; Castellano Escuder, Pol; Gris Oliver, Albert; Canals Suris, Francesc; Sánchez Pla, Alex; Serra, Violeta; Zamora, Esther; Arribas, Joaquin; Saura, Cristina; Tabernero, Josep; Villanueva Cardús, Josep (MDPI, 2022-05-23)

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy

Kagiava, Alexia; Karaiskos, Christos; Lapathitis, George; Heslegrave, Amanda; Sargiannidou, Irene; Zetterberg, Henrik; Bosch, Assumpció (Cell Press, 2023-09-14)

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice

Mòdol-Caballero, Guillem; Herrando-Grabulosa, Mireia; Verdés Franquesa, Sergi; García-Lareu, Belén; Hernández, Neus; Francos-Quijorna, Isaac; Bosch Merino, Assumpció (Frontiers Media, 2021-09-22)

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey

Vermunicht, Paulien; Grecu, Mihaela; Buckley, Claire M.; Pala Vila, Elena; Mairesse, Georges H.; Deharo, Jean-Claude (Frontiers Media, 2023-02-15)

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients

Machuca, Candela; Correa Vela, Marta; García-Navas, Deyanira; Darling, Alejandra; Villalón-García, Irene; Sánchez-Alcázar, José Antonio; Perez Dueñas, Belen (Elsevier, 2021-05)

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Arias-Salgado, Elena G.; Galvez, Eva; Planas-Cerezales, Lurdes; Pintado-Berninches, Laura; Vallespin, Elena; Martinez, Pilar; Martín Nalda, Andrea; Díaz de Heredia Rubio, Maria Cristina; Martínez Gallo, Mónica; Uria Oficialdegui, Maria Luz (BMC, 2019-04-17)

Genetic association study of childhood aggression across raters, instruments, and age

Ip, Hill F.; van der Laan, Camiel M.; Krapohl, Eva M. L.; Brikell, Isabell; Sanchez Mora, Cristina P; Nolte, Ilja M.; Soler Artigas, Maria; Rovira Lorente, Paula; Bosch Munso, Rosa M; Español Martín, Gemma; Ramos Quiroga, José Antonio; Casas Brugué, Miquel; Ribases Haro, Marta (Springer Nature, 2021-07-30)

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome

Sahi, Nitin; Haider, Lukas; Chung, Karen; Kanber, Baris; Samson, Rebecca; Tur Gomez, Carmen; Prados Carrasco, Ferran (Oxford University Press, 2023)

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Martinez de LaPiscina Martin, Idoia; Kouri, Chrysanthi; Aurrekoetxea, Josu; Sanchez, Mirian; Naamneh Elzenaty, Rawda; Sauter, Kay-Sara; Camats Tarruella, Núria (Public Library of Science, 2023-07-11)

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Harder, Aster V. E.; Winsvold, Bendik S.; Noordam, Raymond; Vijfhuizen, Lisanne S.; Børte, Sigrid; Kogelman, Lisette J. A.; Pozo Rosich, Patricia (MDPI, 2021-08)

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients

López‑Cotarelo, Pilar; González‑Jiménez, Adela; Agudo‑Jiménez, Teresa; Abarca Zabalía, Judith; Pilo, Belén; Comabella Lopez, Manuel; Aladro, Yolanda (Nature Research, 2021-11-01)

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations

Farinango, Camila; Gallardo-Cóndor, Jennifer; Freire Paspuel, Byron; Flores-Espinoza, Rodrigo; Jaramillo-Koupermann, Gabriela; López-Cortés, Andrés (MDPI, 2022-06-10)

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease

Sáez, M. E.; González-Pérez, A.; Hernández-Olasagarre, B.; Beà, Aida; Moreno-Grau, S.; de Rojas, Itziar; Comella Carnice, Joan X. (Nature Publishing Group, 2019-11-13)

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment

Maisterra Santos, Olga; Jimenez Balado, Joan; Carrera, Caty; Torres‑Aguila, Nuria P.; Muiño, Elena; Cullell, Natalia (Nature Research, 2021-03-25)

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells

Mena, Jorge; Alloza, Iraide; Tulloch Navarro, Raquel; Aldekoa, Ane; Díez García, Javier; Villanueva Etxebarria, Ane; Midaglia Fernandez, Luciana; Montalban Gairín, Xavier; Comabella Lopez, Manuel; Malhotra Sareen, Sunny (Frontiers Media, 2022-01)

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool

Villafranca Magdalena, Beatriz; Masferrer Ferragutcasas, Carina; Lopez Gil, Carlos; Coll De la Rubia, Eva; Rebull Santamaria, Marta; Parra, Genis; García Jiménez, Angel; Cabrera Diaz, Silvia; Colas Ortega, Eva; Gil Moreno, Antonio; Moiola, Cristian Pablo; Reques Llanos, Armando (MDPI, 2022-06-03)

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

Duperron, Marie-Gabrielle; Knol, Maria; Le Grand, Quentin; Evans, Tavia; Mishra, Aniket; Tsuchida, Ami; Delgado Martínez, Maria Pilar (Springer Nature, 2023-04)

Scientia. Dipòsit d'Informació Digital del Departament de Salut

Visualitzant VHIR - Articles científics per títol

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Gait analysis under the lens of statistical physics

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Genetic association study of childhood aggression across raters, instruments, and age

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

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Visualitzant VHIR - Articles científics per títol

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders ﻿

Gait analysis under the lens of statistical physics ﻿

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis ﻿

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells ﻿

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy ﻿

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice ﻿

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey ﻿

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients ﻿

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes ﻿

Genetic association study of childhood aggression across raters, instruments, and age ﻿

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome ﻿

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations ﻿

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache ﻿

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients ﻿

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations ﻿

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease ﻿

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment ﻿

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells ﻿

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool ﻿

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease ﻿

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Guies i ajudes

Directe a...

Coneix Scientia

Guies i ajudes

Directe a...

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Gait analysis under the lens of statistical physics

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Genetic association study of childhood aggression across raters, instruments, and age

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease