Results 91 to 100 of about 23,427,651 (311)

METU-SNP: An Integrated Software System for SNPComplex Disease Association Analysis

open access: yesJournal of Integrative Bioinformatics, 2011
Summary Recently, there has been increasing research to discover genomic biomarkers, haplotypes, and potentially other variables that together contribute to the development of diseases. Single Nucleotide Polymorphisms (SNPs) are the most common form of genomic variations and they can represent an individual’s genetic variability in greatest detail ...
Gürkan Üstünkar, Yesim Aydin Son
openaire   +3 more sources

SNP-index information of the three markers.

open access: yes, 2016
SNP-index information of the three markers.
Yuanjun Ye (2872955)   +7 more
core   +1 more source

THSD7A Exacerbates Atherosclerosis via Activation of Signaling Axis αvβ3/CEBPD/IL1A

open access: yesAdvanced Science, EarlyView.
THSD7A exerts pro‐inflammatory effects and exacerbates atherosclerosis. Mechanistically, THSD7A regulates endothelial cell inflammation and atherosclerosis by activating the αvβ3/CEBPD/IL1A signaling axis. THSD7A is not only a genetic marker but also a potential therapeutic target for coronary artery disease (CAD).
Jiankun Liu   +15 more
wiley   +1 more source

Similarity Measures for Clustering SNP and Epidemiological Data [PDF]

open access: yes
The issue of suitable similarity measures for a joint consideration of so called SNP data and epidemiological variables arises from the GENICA (Interdisciplinary Study Group on Gene Environment Interaction and Breast Cancer in Germany) casecontrol study ...
Selinski, Silvia
core  

DIXDC1 Promotes Lymphatic Metastasis and Resistance to Cuproptosis in Bladder Cancer Through Mediating DLAT

open access: yesAdvanced Science, EarlyView.
DIXDC1 drives bladder cancer progression by binding and stabilizing DLAT. This axis enhances NEK7 and CCNE2 mRNA stability to promote proliferation and lymphatic metastasis, while limiting copper‐induced DLAT oligomerization to reduce cuproptosis sensitivity, identifying DIXDC1 as a potential target linking metastasis with cuproptosis resistance ...
Hongqiong Li   +17 more
wiley   +1 more source

Association of EGFR and EGF gene polymorphisms with cervical cancer in a case–control study and cross-cancer meta-analysis

open access: yesScientific Reports
Cervical cancer (CC) is one of the most prevalent cancers worldwide. Single nucleotide polymorphisms (SNPs) of the epidermal growth factor receptor (EGFR) and epidermal growth factor (EGF) genes are associated with cancers in diverse populations; However,
Yuhan Shi   +7 more
doaj   +1 more source

SNP-PHAGE – High throughput SNP discovery pipeline

open access: yesBMC Bioinformatics, 2006
Background Single nucleotide polymorphisms (SNPs) as defined here are single base sequence changes or short insertion/deletions between or within individuals of a given species.
Cregan Perry B   +5 more
doaj   +1 more source

SNPs analysis of height traits in Ningqiang pony

open access: yesAnimal Biotechnology, 2020
Ningqiang pony is one of the five pony breeds in China and is listed as a rare species. It is, therefore, meaningful to conduct stature research on this breed for its efficient reproduction, utilization and protection. This study is based on four SNP variants of adjacent LCORL/NCAPG, HMGA2, ZFAT and LASP1 genes, which have been found to be associated ...
Hao Bai   +5 more
openaire   +2 more sources

Similarity Measures for Clustering SNP Data [PDF]

open access: yes
The issue of suitable similarity measures for a particular kind of genetic data – so called SNP data – arises from the GENICA (Interdisciplinary Study Group on Gene Environment Interaction and Breast Cancer in Germany) case-control study of sporadic ...
Ickstadt, Katja, Selinski, Silvia
core  

TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non‐Syndromic Hearing Loss

open access: yesAdvanced Science, EarlyView.
TECTB is a non‐collagenous protein of the tectorial membrane – an extracellular matrix of the cochlea. This study identifies dominant missense variants in TECTB linked to human hereditary deafness in two unrelated families. Genetically engineered mice homozygous for one of the variants are profoundly deaf, whereas heterozygous mice have normal hearing ...
Evan B. Hale   +23 more
wiley   +1 more source

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