ADAM10 c.1804+115T>C

Variant ID: 15-58903083-A-G

NM_001110.2(ADAM10):c.1804+115T>C

This variant was identified in 14 publications

View GRCh38 version.




Publications:


Potential impact of ADAM-10 genetic variants with the clinical features of oral squamous cell carcinoma.

Journal Of Cellular And Molecular Medicine
Chen, Yi-Tzu YT; Lin, Chiao-Wen CW; Chou, Ying-Erh YE; Su, Shih-Chi SC; Chang, Lun-Ching LC; Lee, Chia-Yi CY; Hsieh, Ming-Ju MJ; Yang, Shun-Fa SF
Publication Date: 2023-03-22

Variant appearance in text: rs2305421
PubMed Link: 36946281
Variant Present in the following documents:
  • Main text
  • JCMM-27-1144.pdf
View BVdb publication page



Friend, Foe or Both? Immune Activity in Alzheimer's Disease.

Frontiers In Aging Neuroscience
Frost, Georgia R GR; Jonas, Lauren A LA; Li, Yue-Ming YM
Publication Date: 2019

Variant appearance in text: rs2305421
PubMed Link: 31920620
Variant Present in the following documents:
  • Main text
  • fnagi-11-00337.pdf
View BVdb publication page



Microglia in Alzheimer's Disease: Exploring How Genetics and Phenotype Influence Risk.

Journal Of Molecular Biology
McQuade, Amanda A; Blurton-Jones, Mathew M
Publication Date: 2019-04-19

Variant appearance in text: rs2305421
PubMed Link: 30738892
Variant Present in the following documents:
  • Main text
View BVdb publication page



Influence of ADAM10 Polymorphisms on Plasma Level of Soluble Receptor for Advanced Glycation End Products and The Association With Alzheimer's Disease Risk.

Frontiers In Genetics
Huang, Wen-Hui WH; Chen, Wei W; Jiang, Lian-Ying LY; Yang, Yi-Xia YX; Yao, Li-Fen LF; Li, Ke-Shen KS
Publication Date: 2018

Variant appearance in text: rs2305421
PubMed Link: 30555509
Variant Present in the following documents:
  • Main text
  • fgene-09-00540.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: ADAM10: 1804+115T>C; rs2305421
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
View BVdb publication page



Impact of ADAM10 gene polymorphisms on hepatocellular carcinoma development and clinical characteristics.

International Journal Of Medical Sciences
Shiu, Jr-Shiang JS; Hsieh, Ming-Ju MJ; Chiou, Hui-Ling HL; Wang, Hsiang-Ling HL; Yeh, Chao-Bin CB; Yang, Shun-Fa SF; Chou, Ying-Erh YE
Publication Date: 2018

Variant appearance in text: rs2305421
PubMed Link: 30275760
Variant Present in the following documents:
  • Main text
  • ijmsv15p1334.pdf
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs2305421
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Genes associated with Alzheimer's disease: an overview and current status.

Clinical Interventions In Aging
Giri, Mohan M; Zhang, Man M; Lü, Yang Y
Publication Date: 2016

Variant appearance in text: rs2305421
PubMed Link: 27274215
Variant Present in the following documents:
  • Main text
  • cia-11-665.pdf
View BVdb publication page



Association of a BACE1 Gene Polymorphism with Parkinson's Disease in a Norwegian Population.

Parkinson'S Disease
Lange, Johannes J; Lunde, Kristin Aaser KA; Sletten, Camilla C; Møller, Simon Geir SG; Tysnes, Ole-Bjørn OB; Alves, Guido G; Larsen, Jan Petter JP; Maple-Grødem, Jodi J
Publication Date: 2015

Variant appearance in text: rs2305421
PubMed Link: 26788404
Variant Present in the following documents:
  • Main text
  • PD2015-973298.pdf
View BVdb publication page



Cerebrospinal fluid Aβ42 levels and APP processing pathway genes in Parkinson's disease.

Movement Disorders : Official Journal Of The Movement Disorder Society
Bekris, Lynn M LM; Tsuang, Debby W DW; Peskind, Elaine R ER; Yu, Chang E CE; Montine, Thomas J TJ; Zhang, Jing J; Zabetian, Cyrus P CP; Leverenz, James B JB
Publication Date: 2015-06

Variant appearance in text: rs2305421
PubMed Link: 25808939
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of rare variants in Alzheimer's disease.

Frontiers In Genetics
Lord, Jenny J; Lu, Alexander J AJ; Cruchaga, Carlos C
Publication Date: 2014

Variant appearance in text: rs2305421
PubMed Link: 25389433
Variant Present in the following documents:
  • Main text
  • fgene-05-00369.pdf
View BVdb publication page



An association study on ADAM10 promoter polymorphisms and atherosclerotic cerebral infarction in a Chinese population.

Cns Neuroscience & Therapeutics
Li, You Y; Liao, Feng F; Yin, Xiao-Jian XJ; Cui, Li-Li LL; Ma, Guo-Da GD; Nong, Xiao-Xian XX; Zhou, Hai-Hong HH; Chen, Yan-Fang YF; Zhao, Bin B; Li, Ke-Shen KS
Publication Date: 2013-10

Variant appearance in text: rs2305421
PubMed Link: 23773531
Variant Present in the following documents:
  • Main text
  • CNS-19-785.pdf
View BVdb publication page



Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease.

Neurobiology Of Aging
Bekris, L M LM; Galloway, N M NM; Millard, S S; Lockhart, D D; Li, G G; Galasko, D R DR; Farlow, M R MR; Clark, C M CM; Quinn, J F JF; Kaye, J A JA; Schellenberg, G D GD; Leverenz, J B JB; Seubert, P P; Tsuang, D W DW; Peskind, E R ER; Yu, C E CE
Publication Date: 2011-03

Variant appearance in text: rs2305421
PubMed Link: 21196064
Variant Present in the following documents:
  • Main text
View BVdb publication page



Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate {alpha}-secretase activity.

Human Molecular Genetics
Kim, Minji M; Suh, Jaehong J; Romano, Donna D; Truong, Mimy H MH; Mullin, Kristina K; Hooli, Basavaraj B; Norton, David D; Tesco, Giuseppina G; Elliott, Kathy K; Wagner, Steven L SL; Moir, Robert D RD; Becker, K David KD; Tanzi, Rudolph E RE
Publication Date: 2009-10-15

Variant appearance in text: rs2305421
PubMed Link: 19608551
Variant Present in the following documents:
  • Main text
View BVdb publication page