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BMC Molecular Biology
|
May 13, 2010
The human RPS4 paralogue on Yq11.223 encodes a structurally conserved ribosomal protein and is preferentially expressed during spermatogenesis
Alexandra M Lopes, Ricardo N Miguel, Carole A Sargent, et al.
Plos Genetics
|
September 22, 2017
Forensic genetics and genomics: Much more than just a human affair
Miguel Arenas, Filipe Pereira, Manuela Oliveira, et al.
Genome Biology and Evolution
|
March 12, 2026
Retrotransposition events shape the evolution of the ataxin-3 gene family in primates
Daniela Felício, Maria Inês Martins, Andreia Pinto, et al.
Brain Sciences
|
May 28, 2022
A High Methylation Level of a Novel -284 bp CpG Island in the <i>RAMP1</i> Gene Promoter Is Potentially Associated with Migraine in Women
Estefânia Carvalho, Andreia Dias, Alda Sousa, et al.
BMC Genomics
|
February 4, 2010
Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome
Alexandra M Lopes, Paul S Burgoyne, Andrew Ojarikre, et al.
Briefings in Functional Genomics
|
May 31, 2023
Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease
Daniela Felício, Miguel Alves-Ferreira, Mariana Santos, et al.
The Journal of Headache and Pain
|
June 28, 2023
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility
Daniela Felício, Andreia Dias, Sandra Martins, et al.
Scientific Reports
|
October 15, 2021
Influence of PICALM and CLU risk variants on beta EEG activity in Alzheimer's disease patients
Aarón Maturana-Candelas, Carlos Gómez, Jesús Poza, et al.
Sensors (Basel, Switzerland)
|
July 16, 2020
Relationship between the Presence of the <i>ApoE ε</i>4 Allele and EEG Complexity along the Alzheimer's Disease Continuum
Víctor Gutiérrez-de Pablo, Carlos Gómez, Jesús Poza, et al.
Reproductive Biomedicine Online
|
June 11, 2014
A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia
Catarina M Seabra, Sofia Quental, Ana Paula Neto, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
BMC Molecular Biology
|
May 13, 2010
The human RPS4 paralogue on Yq11.223 encodes a structurally conserved ribosomal protein and is preferentially expressed during spermatogenesis
Alexandra M Lopes, Ricardo N Miguel, Carole A Sargent, et al.
Plos Genetics
|
September 22, 2017
Forensic genetics and genomics: Much more than just a human affair
Miguel Arenas, Filipe Pereira, Manuela Oliveira, et al.
Genome Biology and Evolution
|
March 12, 2026
Retrotransposition events shape the evolution of the ataxin-3 gene family in primates
Daniela Felício, Maria Inês Martins, Andreia Pinto, et al.
Brain Sciences
|
May 28, 2022
A High Methylation Level of a Novel -284 bp CpG Island in the <i>RAMP1</i> Gene Promoter Is Potentially Associated with Migraine in Women
Estefânia Carvalho, Andreia Dias, Alda Sousa, et al.
BMC Genomics
|
February 4, 2010
Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome
Alexandra M Lopes, Paul S Burgoyne, Andrew Ojarikre, et al.
Briefings in Functional Genomics
|
May 31, 2023
Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease
Daniela Felício, Miguel Alves-Ferreira, Mariana Santos, et al.
The Journal of Headache and Pain
|
June 28, 2023
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility
Daniela Felício, Andreia Dias, Sandra Martins, et al.
Scientific Reports
|
October 15, 2021
Influence of PICALM and CLU risk variants on beta EEG activity in Alzheimer's disease patients
Aarón Maturana-Candelas, Carlos Gómez, Jesús Poza, et al.
Sensors (Basel, Switzerland)
|
July 16, 2020
Relationship between the Presence of the <i>ApoE ε</i>4 Allele and EEG Complexity along the Alzheimer's Disease Continuum
Víctor Gutiérrez-de Pablo, Carlos Gómez, Jesús Poza, et al.
Reproductive Biomedicine Online
|
June 11, 2014
A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia
Catarina M Seabra, Sofia Quental, Ana Paula Neto, et al.
Page
of 5