Varaico: Literature-Extracted Genetic Variants

Gene:SNCA
Variant:p.M1I
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SNCA

NM_000345.4:p.M1I

Associated Papers

Relationship between single-nucleotide polymorphisms and cancer immunotherapy efficacy and toxicity: a systematic review.

Specchia M et al.

Frontiers in Oncology, 2025

Association between PD-1 single nucleotide gene variants and the risk of metastatic melanoma.

Boutros A et al.

Archives of Dermatological Research, 2024

The predictive and prognostic role of single nucleotide gene variants of PD-1 and PD-L1 in patients with advanced melanoma treated with PD-1 inhibitors.

Boutros A et al.

Immuno-oncology Technology, 2023

A Downsized and Optimised Intracellular Library-Derived Peptide Prevents Alpha-Synuclein Primary Nucleation and Toxicity Without Impacting Upon Lipid Binding.

Meade RM et al.

Journal of Molecular Biology, 2021

The ATP Synthase Deficiency in Human Diseases.

Galber C et al.

Life (basel, Switzerland), 2021

Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.

Sarparanta J et al.

International Journal of Molecular Sciences, 2020

Effects of the programmed cell death 1 (PDCD1) polymorphisms in susceptibility to systemic lupus erythematosus.

Fathi F et al.

International Journal of Immunogenetics, 2020

Immune Checkpoint Molecules-Inherited Variations as Markers for Cancer Risk.

Wagner M et al.

Frontiers in Immunology, 2020

Association of programmed death-1 gene polymorphisms with the risk of basal cell carcinoma.

Fathi F et al.

International Journal of Immunogenetics, 2019

Programmed cell death 1 gene polymorphism as a possible risk for systemic lupus erythematosus in Egyptian females.

Abo El-Khair SM et al.

Lupus, 2019

PD-1 genotype of the donor is associated with acute graft-versus-host disease after HLA-identical sibling donor stem cell transplantation.

Santos N et al.

Annals of Hematology, 2018

Autoimmune and immunogenetic profile of patients with optic neuritis in a population-based cohort.

Soelberg K et al.

Multiple Sclerosis and Related Disorders, 2018

Site-specific copper-catalyzed oxidation of α-synuclein: tightening the link between metal binding and protein oxidative damage in Parkinson's disease.

Miotto MC et al.

Inorganic Chemistry, 2014

Polymorphisms in PDCD1 gene are not associated with aplastic anemia in Chinese Han population.

Ming ZJ et al.

Rheumatology International, 2012

Association of a PDCD1 polymorphism with renal manifestations in systemic lupus erythematosus.

Johansson M et al.

Arthritis and Rheumatism, 2005

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."