Results 21 to 30 of about 3,634,544 (343)

Tapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study [PDF]

open access: yes, 2005
Juvenile rheumatoid arthritis (JRA) comprises a group of chronic systemic inflammatory disorders that primarily affect joints and can cause long-term disability.
Bukulmez, H   +9 more
core   +2 more sources

Construction of Genetic Linkage Map of Plum (Prunus salicina L.) with ISSR and SRAP Markers

open access: yesGuangdong nongye kexue, 2022
【Objective】Plum (Prunus salicina L.) is a tree species with great economic prospect in northeast China, and it has important social and economic values. Genetic linkage maps of plum were constructed by molecular markers to provide a theoretical basis for
Lili SUN   +4 more
doaj   +1 more source

A saturated genetic linkage map of autotetraploid alfalfa (Medicago sativa L.) developed using genotyping-by-sequencing is highly syntenous with the Medicago truncatula genome. [PDF]

open access: yes, 2014
A genetic linkage map is a valuable tool for quantitative trait locus mapping, map-based gene cloning, comparative mapping, and whole-genome assembly. Alfalfa, one of the most important forage crops in the world, is autotetraploid, allogamous, and highly
Acharya, Ananta   +5 more
core   +2 more sources

Construction of Agropyron Gaertn. genetic linkage maps using a wheat 660K SNP array reveals a homoeologous relationship with the wheat genome

open access: yesPlant Biotechnology Journal, 2017
Summary Agropyron Gaertn. (P genome) is a wild relative of wheat that harbours many genetic variations that could be used to increase the genetic diversity of wheat.
Shenghui Zhou   +9 more
semanticscholar   +1 more source

High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. [PDF]

open access: yes, 2009
Chromosome 17q11-q21 is a region of the genome likely to harbor susceptibility to autism (MIM(209850)) based on earlier evidence of linkage to the disorder.
Cantor, RM   +6 more
core   +3 more sources

An extremely rare association of Dyggve-Melchior-Clausen syndrome with mania: Coincidence or comorbidity

open access: yesIndian Journal of Psychological Medicine, 2015
Dyggve-Melchior-Clausen syndrome is a progressive spondylo-epi-metaphyseal dysplasia associated with mental retardation, characterized by a triad of skeletal deformities (short trunk dwarfism, scoliosis, microcephaly, and limb deformities), facial ...
Sujita Kumar Kar   +2 more
doaj   +1 more source

Mapping genes through the use of linkage disequilibrium generated by genetic drift: 'Drift mapping' in small populations with no demographic expansion [PDF]

open access: yes, 1998
Linkage disequilibrium has been a powerful tool in identifying rare disease alleles in human populations. To date, most research has been directed to isolated populations which have undergone a bottleneck followed by rapid exponential expansion.
Laan, Maris   +3 more
core   +1 more source

Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01

open access: yesBMC Genomics, 2016
A landmark in soybean research, Glyma1.01, the first whole genome sequence of variety Williams 82 (Glycine max L. Merr.) was completed in 2010 and is widely used.
Q. Song   +7 more
semanticscholar   +1 more source

A gene-derived SNP-based high resolution linkage map of carrot including the location of QTL conditioning root and leaf anthocyanin pigmentation [PDF]

open access: yes, 2014
Purple carrots accumulate large quantities of anthocyanins in their roots and leaves. These flavonoid pigments possess antioxidant activity and are implicated in providing health benefits.
Cavagnaro, Pablo Federico   +6 more
core   +2 more sources

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.

open access: yesAmerican Journal of Human Genetics, 1998
The contribution of BRCA1 and BRCA2 to inherited breast cancer was assessed by linkage and mutation analysis in 237 families, each with at least four cases of breast cancer, collected by the Breast Cancer Linkage Consortium.
D. Ford   +37 more
semanticscholar   +1 more source

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