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Journal for Immunotherapy of Cancer
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December 2, 2022
T cells of colorectal cancer patients' stimulated by neoantigenic and cryptic peptides better recognize autologous tumor cells
Sandra Schwarz, Johanna Schmitz, Markus W Löffler, et al.
NPJ Parkinson'S Disease
|
April 15, 2024
Resequencing the complete SNCA locus in Indian patients with Parkinson's disease
Asha Kishore, Marc Sturm, Kanchana Soman Pillai, et al.
Parkinsonism & Related Disorders
|
August 30, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases
Ai Huey Tan, Katja Lohmann, Yi Wen Tay, et al.
European Journal of Human Genetics : EJHG
|
May 29, 2021
Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery
Holger Hengel, Rebecca Buchert, Marc Sturm, et al.
Economics and Human Biology
|
March 5, 2011
Relative weight-related costs of healthcare use by children--results from the two German birth cohorts, GINI-plus and LISA-plus
Ariane Breitfelder, Christina M Wenig, Silke B Wolfenstetter, et al.
Allergy
|
September 7, 2022
Allergic disease trajectories up to adolescence: Characteristics, early-life, and genetic determinants
Anna Kilanowski, Elisabeth Thiering, Gang Wang, et al.
American Journal of Human Genetics
|
November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5A
Chanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
Journal of Movement Disorders
|
January 23, 2024
A Case of 18p Chromosomal Deletion Encompassing GNAL in a Patient With Dystonia-Parkinsonism
Giulia Di Rauso, Francesco Cavallieri, Edoardo Monfrini, et al.
Brain : a Journal of Neurology
|
April 23, 2019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
Anja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Orphanet Journal of Rare Diseases
|
August 29, 2019
Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome
Claudia Cozma, Marina Hovakimyan, Marius-Ionuț Iurașcu, et al.
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of 59
Search research articles
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Showing results (401-410 of 585) with videos related to
Sort By:
Page
of 59
Journal for Immunotherapy of Cancer
|
December 2, 2022
T cells of colorectal cancer patients' stimulated by neoantigenic and cryptic peptides better recognize autologous tumor cells
Sandra Schwarz, Johanna Schmitz, Markus W Löffler, et al.
NPJ Parkinson'S Disease
|
April 15, 2024
Resequencing the complete SNCA locus in Indian patients with Parkinson's disease
Asha Kishore, Marc Sturm, Kanchana Soman Pillai, et al.
Parkinsonism & Related Disorders
|
August 30, 2020
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases
Ai Huey Tan, Katja Lohmann, Yi Wen Tay, et al.
European Journal of Human Genetics : EJHG
|
May 29, 2021
Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery
Holger Hengel, Rebecca Buchert, Marc Sturm, et al.
Economics and Human Biology
|
March 5, 2011
Relative weight-related costs of healthcare use by children--results from the two German birth cohorts, GINI-plus and LISA-plus
Ariane Breitfelder, Christina M Wenig, Silke B Wolfenstetter, et al.
Allergy
|
September 7, 2022
Allergic disease trajectories up to adolescence: Characteristics, early-life, and genetic determinants
Anna Kilanowski, Elisabeth Thiering, Gang Wang, et al.
American Journal of Human Genetics
|
November 22, 2016
Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5A
Chanshuai Han, Reem Alkhater, Tawfiq Froukh, et al.
Journal of Movement Disorders
|
January 23, 2024
A Case of 18p Chromosomal Deletion Encompassing GNAL in a Patient With Dystonia-Parkinsonism
Giulia Di Rauso, Francesco Cavallieri, Edoardo Monfrini, et al.
Brain : a Journal of Neurology
|
April 23, 2019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
Anja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Orphanet Journal of Rare Diseases
|
August 29, 2019
Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome
Claudia Cozma, Marina Hovakimyan, Marius-Ionuț Iurașcu, et al.
Page
of 59