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American Journal of Medical Genetics. Part A
|
February 13, 2009
Novel UBE3A mutations causing Angelman syndrome: different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions
Cristina Camprubí, Miriam Guitart, Elisabeth Gabau, et al.
Pain
|
March 4, 2014
Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system
Elisa Docampo, Georgia Escaramís, Mònica Gratacòs, et al.
European Journal of Cancer (Oxford, England : 1990)
|
July 8, 2025
Molecular determinants of survival in metastatic uveal melanoma: The impact of SF3B1 mutations
Luis P Del Carpio, Mar Varela, Mikel Portu, et al.
Plos Genetics
|
March 22, 2014
Validation and genotyping of multiple human polymorphic inversions mediated by inverted repeats reveals a high degree of recurrence
Cristina Aguado, Magdalena Gayà-Vidal, Sergi Villatoro, et al.
Nature Communications
|
September 19, 2019
Evolutionary and functional impact of common polymorphic inversions in the human genome
Carla Giner-Delgado, Sergi Villatoro, Jon Lerga-Jaso, et al.
Frontiers in Medicine
|
January 10, 2017
Liquid Biopsy in Non-Small Cell Lung Cancer
Miguel A Molina-Vila, Clara Mayo-de-Las-Casas, Ana Giménez-Capitán, et al.
Virchows Archiv : an International Journal of Pathology
|
April 7, 2026
Homologous recombination deficiency tumor tissue testing in a real-world cohort of tubo-ovarian carcinoma patients: validation of decentralized genomic profiling in 4777 cases
Federico Rojo, Conxi Lazaro, Ihab Abdulkader-Nallib, et al.
European Journal of Cancer (Oxford, England : 1990)
|
April 10, 2026
Implementing a molecular prescreening strategy for tumors without public NGS access in a cancer center network: Results from the PREICO project
Paula Sàbat, Maria Ajenjo-Bauza, Cinta Hierro, et al.
Translational Cancer Research
|
February 4, 2022
Prospective analysis of liquid biopsies of advanced non-small cell lung cancer patients after progression to targeted therapies using GeneReader NGS platform
Clara Mayo de Las Casas, Mónica Garzón-Ibañez, Núria Jordana-Ariza, et al.
Nature
|
September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
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Showing results (11-20 of 20) with videos related to
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This site can display upto 20 results.
American Journal of Medical Genetics. Part A
|
February 13, 2009
Novel UBE3A mutations causing Angelman syndrome: different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions
Cristina Camprubí, Miriam Guitart, Elisabeth Gabau, et al.
Pain
|
March 4, 2014
Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system
Elisa Docampo, Georgia Escaramís, Mònica Gratacòs, et al.
European Journal of Cancer (Oxford, England : 1990)
|
July 8, 2025
Molecular determinants of survival in metastatic uveal melanoma: The impact of SF3B1 mutations
Luis P Del Carpio, Mar Varela, Mikel Portu, et al.
Plos Genetics
|
March 22, 2014
Validation and genotyping of multiple human polymorphic inversions mediated by inverted repeats reveals a high degree of recurrence
Cristina Aguado, Magdalena Gayà-Vidal, Sergi Villatoro, et al.
Nature Communications
|
September 19, 2019
Evolutionary and functional impact of common polymorphic inversions in the human genome
Carla Giner-Delgado, Sergi Villatoro, Jon Lerga-Jaso, et al.
Frontiers in Medicine
|
January 10, 2017
Liquid Biopsy in Non-Small Cell Lung Cancer
Miguel A Molina-Vila, Clara Mayo-de-Las-Casas, Ana Giménez-Capitán, et al.
Virchows Archiv : an International Journal of Pathology
|
April 7, 2026
Homologous recombination deficiency tumor tissue testing in a real-world cohort of tubo-ovarian carcinoma patients: validation of decentralized genomic profiling in 4777 cases
Federico Rojo, Conxi Lazaro, Ihab Abdulkader-Nallib, et al.
European Journal of Cancer (Oxford, England : 1990)
|
April 10, 2026
Implementing a molecular prescreening strategy for tumors without public NGS access in a cancer center network: Results from the PREICO project
Paula Sàbat, Maria Ajenjo-Bauza, Cinta Hierro, et al.
Translational Cancer Research
|
February 4, 2022
Prospective analysis of liquid biopsies of advanced non-small cell lung cancer patients after progression to targeted therapies using GeneReader NGS platform
Clara Mayo de Las Casas, Mónica Garzón-Ibañez, Núria Jordana-Ariza, et al.
Nature
|
September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
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