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Laryngoscope Investigative Otolaryngology
|
February 14, 2022
Gene expression profiling for metastatic risk in head and neck cutaneous squamous cell carcinoma
Sarah T Arron, Ashley Wysong, Mary A Hall, et al.
Epilepsia
|
October 1, 2008
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy
Dongsheng Bai, Julia N Bailey, Reyna M Durón, et al.
BMC Proceedings
|
December 19, 2014
Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees
Heike Bickeböller, Julia N Bailey, Joseph Beyene, et al.
Cancer Research
|
August 17, 2005
The protein kinase Cbeta-selective inhibitor, Enzastaurin (LY317615.HCl), suppresses signaling through the AKT pathway, induces apoptosis, and suppresses growth of human colon cancer and glioblastoma xenografts
Jeremy R Graff, Ann M McNulty, Kimberly Ross Hanna, et al.
American Journal of Human Genetics
|
June 3, 2008
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy
Miyabi Tanaka, Richard W Olsen, Marco T Medina, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
August 8, 2025
Integration of crop modeling and sensing into molecular breeding for nutritional quality and stress tolerance
Jonathan Berlingeri, Abelina Fuentes, Earl Ranario, et al.
Advances in Neurology
|
October 29, 2004
Familial juvenile myoclonic epilepsy
María Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, et al.
Journal of Internal Medicine
|
August 4, 2020
Use of the IL-6R antagonist tocilizumab in hospitalized COVID-19 patients
K Patel, T A Gooley, N Bailey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 29, 2016
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality
Julia N Bailey, Christopher Patterson, Laurence de Nijs, et al.
Neurology
|
May 30, 2008
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy
M T Medina, T Suzuki, M E Alonso, et al.
Page
of 40
Search research articles
Search
Showing results (381-390 of 400) with videos related to
Sort By:
Page
of 40
Laryngoscope Investigative Otolaryngology
|
February 14, 2022
Gene expression profiling for metastatic risk in head and neck cutaneous squamous cell carcinoma
Sarah T Arron, Ashley Wysong, Mary A Hall, et al.
Epilepsia
|
October 1, 2008
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy
Dongsheng Bai, Julia N Bailey, Reyna M Durón, et al.
BMC Proceedings
|
December 19, 2014
Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees
Heike Bickeböller, Julia N Bailey, Joseph Beyene, et al.
Cancer Research
|
August 17, 2005
The protein kinase Cbeta-selective inhibitor, Enzastaurin (LY317615.HCl), suppresses signaling through the AKT pathway, induces apoptosis, and suppresses growth of human colon cancer and glioblastoma xenografts
Jeremy R Graff, Ann M McNulty, Kimberly Ross Hanna, et al.
American Journal of Human Genetics
|
June 3, 2008
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy
Miyabi Tanaka, Richard W Olsen, Marco T Medina, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
August 8, 2025
Integration of crop modeling and sensing into molecular breeding for nutritional quality and stress tolerance
Jonathan Berlingeri, Abelina Fuentes, Earl Ranario, et al.
Advances in Neurology
|
October 29, 2004
Familial juvenile myoclonic epilepsy
María Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, et al.
Journal of Internal Medicine
|
August 4, 2020
Use of the IL-6R antagonist tocilizumab in hospitalized COVID-19 patients
K Patel, T A Gooley, N Bailey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 29, 2016
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality
Julia N Bailey, Christopher Patterson, Laurence de Nijs, et al.
Neurology
|
May 30, 2008
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy
M T Medina, T Suzuki, M E Alonso, et al.
Page
of 40