Searching journal content for articles similar to Nechiporuk et al. 9 (12): 1231.

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  1. ...understood. Here, we use comparative genomics, expression across multiple ontogenetic stages and tissues, as well as polymorphism data to investigate MHC evolution in newts. Contrary to earlier suggestions of a massively expanded MHC in salamanders, we find that the core MHC region remains relatively compact...
  2. ...Primate segmental duplication creates novel promoters for the LRRC37 gene family within the 17q21.31 inversion polymorphism region Cemalettin Bekpen 1 , 2 , 5 , Ibrahim Tastekin 2 , Priscillia Siswara 3 , Cezmi A. Akdis 1 and Evan E...
  3. ...Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair Thomas O. Auer 1 , 2 , 3 , 4 , Karine Duroure 1 , 2 , 3 , Anne De Cian 5 , 6 , 7 , Jean-Paul Concordet 5 , 6 , 7 , 8 and Filippo...
  4. ..., but that did not work well in examining the Tas1r3 in zebrafish. Despite this, the feeding preference phenotype exhibited by tas1r3-deficient fish is specific, as assessed by the zebrafish in a double-blind feeding experiment. Collectively, we think that these feeding behavior experiments of tas1r3-deficient...
  5. ...in Drosophila. Mol. Biol. Evol. 13 : 261 – 277 . ↵ Nechiporuk A. , Finney J.E. , Keating M.T. , Johnson S.L. ( 1999 ) Assessment of polymorphism in zebrafish mapping strains. Genome Res. 9 : 1231 – 1238 . ↵ Nickerson D.A. , Tobe V.O. , Taylor S.L. ( 1997 ) Polyphred: Automating the detection and genotyping...
  6. ...Genome-wide analysis of microsatellite polymorphism in chicken circumventing the ascertainment bias Mikael Brandström and Hans Ellegren 1 Department of Evolutionary Biology, Evolutionary Biology Centre, Uppsala University, Norbyvägen 18D, SE-752 36 Uppsala...
  7. ...DNAs were categorized as isolated (Supplemental Fig. S1B and 381 Supplemental Table S1). The correlation between POLR3D and biotin-capture was assessed using the 382 Spearman’s correlation coefficient (r). Statistical differences in log2 integrated tDNA expression levels 383 between clustered and isolated t...
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  8. ...history traits (Etges 1993), behavior (Crowley-Gall et al. 2016), and genomic and transcriptomic differences (Matzkin and Markow 2013; Rajpurohit et al. 2013; Benowitz et al. 2020, 2024; De Panis et al. 2022). However, the contribution of TEs to the evolution of HLAU genes has not yet been assessed. Here...
  9. ...and have been implicated in evolutionary processes, human health, and disease (Eichler 2019; Levy-Sakin et al. 2019). However, this contribution is underestimated, primarily due to the limitation of the available technologies used to assess SVs in the human population and rare disorders, including NTDs...
  10. ...Poecilia wingei and Poecilia obscura (Nanda et al. 2014). This analysis revealed polymorphisms in heterochromatin content of the Y as well as differences in distance of the genetic marker M_229 to the physical chromosome end between populations. The sex determination locus (SDL) was mapped to the most...
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