Results 231 to 240 of about 730,667 (367)

Supplementary Table 1 from Genome-Wide Copy Number Analysis in Esophageal Adenocarcinoma Using High-Density Single-Nucleotide Polymorphism Arrays

, 2023
Derek J. Nancarrow, Herlina Y. Handoko, B. Mark Smithers, D. C. Gotley, Paul A. Drew, David I. Watson, Andrew D. Clouston, Nicholas K. Hayward, David C. Whiteman   +8 more
openalex   +1 more source

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

Bioinform., 2012
S. Lee, Jian Yang, M. Goddard, P. Visscher, N. Wray   +4 more
semanticscholar   +1 more source

Exploring the presence of the GPR126 single nucleotide polymorphism (rs536714306) in periodontal patients of European ancestry. [PDF]

BMC Res Notes
Chatzopoulou E, Fanourakis G, Papanikolaou N, Chatzistamou I, Dereka X, Vastardis H.   +5 more
europepmc   +1 more source

TP53 and MDM2 single nucleotide polymorphisms influence survival in non-del(5q) myelodysplastic syndromes [PDF]

, 2015
Kathy L. McGraw, Thomas Cluzeau, David A. Sallman, Ashley A. Basiorka, Brittany Irvine, Ling Zhang, Pearlie K. Epling‐Burnette, Dana E. Rollison, Mar Mallo, Lubomir Sokol, Françesc Solé, Jaroslaw P. Maciejewski, Alan F. List   +12 more
openalex   +1 more source

Targeting G‐Rich lncRNA and its Structural Polymorphism with Selective G‐Quadruplex Ligands: An NMR Study

Chemistry – A European Journal, EarlyView.
The REG1CP‐derived RNA oligonucleotide SL15P adopts a parallel G‐quadruplex (rGQ) structure. In this study, we investigate the effect of several well‐characterized ligands, originally developed for DNA GQs, on the RNA counterpart, with the aim of evaluating their binding ability and specific binding modes.
Giuseppe Satta, Jasna Brčić, Janez Plavec   +2 more
wiley   +1 more source

Genetic predisposition to porto‐sinusoidal vascular disorder: A functional genomic‐based, multigenerational family study

Hepatology, EarlyView., 2022
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan, André Megarbane, Aziz Chouchane, Deepak Karthik, Ramzi Temanni, Atilio Reyes Romero, Huiying Hua, Chun Pan, Xixi Chen, Murugan Subramanian, Chadi Saad, Hamdi Mbarek, Cybel Mehawej, Eliane Chouery, Sirin W. Abuaqel, Alexander Dömling, Sami Remadi, Cesar Yaghi, Pu Li, Lotfi Chouchane   +19 more
wiley   +1 more source

Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole-Genome Sequencing and Single-Nucleotide Polymorphism Methods [PDF]

, 2016
Carlo G. Artieri, Carrie Haverty, Eric A. Evans, Judith D. Goldberg, Imran S. Haque, Yuval Yaron, Dale Muzzey   +6 more
openalex   +1 more source

Exploration and Characterization of the Antimalarial Activity of Pyrimidine‐2,4‐Diamines for which Resistance is Mediated by the ABCI3 Transporter

ChemMedChem, EarlyView.
Investigation of the structure‐activity relationship on W482 (1) with a pyrimidine‐2,4‐diamine scaffold culminated in analog 51 with enhanced anti‐plasmodial activity. Forward genetics and phenotypic examination revealed the ABCI3 transporter protein as a putative resistance mechanism.
Mahta Mansouri, Madeline G. Dans, Zijun Low, Katie Loi, Kate E. Jarman, Jocelyn S. Penington, Deyun Qiu, Adele M. Lehane, Benigno Crespo, Franciso‐Javier Gamo, Delphine Baud, Stephen Brand, Paul F. Jackson, Alan F. Cowman, Brad E. Sleebs   +14 more
wiley   +1 more source

The Genetic Structure and Diversity of Different Pigeon Breeds Based on a 5 K Single Nucleotide Polymorphism Chip. [PDF]

Animals (Basel)
Hou H, Li X, Wang X, Cai X, Tu Y, Lv W, Shen X, Yang C, Yao J.   +8 more
europepmc   +1 more source

Single nucleotide polymorphisms and penicillin non-susceptibility among invasive Streptococcus pneumoniae from Vietnam and India: Insights from a comparative genomics study

Avani Panickar, Anand Manoharan, Sudha Ramaiah   +2 more
openalex   +1 more source