Results 161 to 170 of about 29,122 (264)

Investigation of MHC-B linked LEI0258 marker diversity in various chicken populations. [PDF]

J Anim Sci Technol
Manjula P, Perera DL, Fernando R, Kim M, Cho E, Lee JH.   +5 more
europepmc   +1 more source

Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis. [PDF]

J Am Soc Nephrol
Vrbacká A, Přistoupilová A, Kidd KO, Janoušek V, Radina M, Vylet'al P, Bitar I, Stránecký V, Steiner-Mrázová L, Trešlová H, Sovová J, Hodaňová K, Hartmannová H, Mušálková D, Svojšová K, Kmochová T, Barešová V, Bleyer H, Taylor A, Martin L, Sanchez A, Ryšavá R, Lajtmanová I, Rajnochová-Bloudíčková S, Viklický O, Papagregoriou G, Deltas C, Stavrou C, Jorge S, Lopes JA, Rodrigues M, Elhassan E, Clince M, Rowan C, Conlon P, Teltsh O, Cavalleri GL, Blumenstiel B, Toledo D, DiStefano M, DeFelice M, Živná M, Bleyer AJ, Kmoch S.   +43 more
europepmc   +1 more source

The Clinical, Genetic, Psychosocial, and Care Landscape of X-Linked Dystonia-Parkinsonism in Filipino Men: A Scoping Review. [PDF]

Am J Mens Health
Ramos MD, Manning J, Harris J, Adorno M, Marye R, Evangelista L.   +5 more
europepmc   +1 more source

Genetic Diversity of Methicillin-Resistant <i>Staphylococcus aureus</i> Isolates From Two Tertiary Care Hospitals in Sulaymaniyah, Iraq, Characterized by <i>spa</i> Typing, Coagulase VNTR Sequencing, and REP-PCR. [PDF]

Int J Microbiol
Shwan AO, Arif SK.
europepmc   +1 more source

Commentary: "<i>TRIB3</i> promoter 33 bp VNTR is associated with the risk of cerebrovascular disease in type 2 diabetic patients". [PDF]

Front Genet
Torbidoni-Baldassari B, Romagnoli L, Napolioni V.   +2 more
europepmc   +1 more source

Genome-wide associations of structural variants with human traits through imputation from long-read assemblies. [PDF]

Nat Genet
Bai WY, Liu S, Duan Z, Yang JJ, Chen J, Hou J, Wu L, Li N, Qi T, Yang J.   +9 more
europepmc   +1 more source

The role of the endothelial nitric oxide synthase variants in the development of juvenile idiopathic arthritis and its clinical findings. [PDF]

Rev Assoc Med Bras (1992)
Dogantan S, Sayin SH, Yücel BB, Taskin SN, Qizi KV, Pehlivan S.   +5 more
europepmc   +1 more source

Association of the <i>eNOS</i> Gene Intron 4 VNTR Polymorphism with Susceptibility to Preeclampsia and Its Severity in an Algerian Cohort. [PDF]

Genes (Basel)
Atmani SM, Bouldjennet F, Khalili Y, Feghoul N, Dammene Debbih A.   +4 more
europepmc   +1 more source

The functional minisatellite at the 3'-UTR of SLC6A3/DAT1 and dementia spectrum disorders: an association study in a population of Central Italy. [PDF]

BMC Med Genomics
Torbidoni-Baldassari B, Guazzarini AG, Rezza G, Bastiani P, Cecchetti R, Mecocci P, Napolioni V.   +6 more
europepmc   +1 more source

The VNTR in complex disorders: the forgotten polymorphisms? A functional way forward?

Genomics, 2013
Keeley J. Brookes
semanticscholar   +1 more source