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Journal of Animal Breeding and Genetics, 2022
AbstractThe objectives of this study were to assess the autosomal and sex‐linked genetic inheritance of growth traits and identify the effective dosage compensation on the Z chromosome in Mazandaran native chickens. The data included body weights at hatching (BW0), 8 weeks (BW8) and 12 weeks (BW12) of age, related to the first 21 generations of ...
Fereshte Kaviani +2 more
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AbstractThe objectives of this study were to assess the autosomal and sex‐linked genetic inheritance of growth traits and identify the effective dosage compensation on the Z chromosome in Mazandaran native chickens. The data included body weights at hatching (BW0), 8 weeks (BW8) and 12 weeks (BW12) of age, related to the first 21 generations of ...
Fereshte Kaviani +2 more
openaire +2 more sources
Gene dosage effects: nonlinearities, genetic interactions, and dosage compensation
Trends in Genetics, 2013High-throughput genomic analyses have shown that many mutations, including loss-of-function (LOF) mutations, are present in diseased as well as in healthy individuals. Gene dosage effects due to deletions, duplications, and LOF mutations provide avenues to explore oligo- and multigenic inheritance. Here, we focus on several mechanisms that mediate gene
Reiner A, Veitia +2 more
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A C. briggsae Genetic Suppressor Screen to Identify Dosage Compensation Pathway Components
Biochemistry & Molecular Biology Journal, 2018Dosage compensation, the process by which the expression of X-linked genes are equalized between males, which have a single X chromosome and females, which have two, is essential in all heterogametic organisms. In C. elegans, dosage compensation is a complex process that is regulated by the developmental switch gene, xol-1.
Jacqueline C Alexander +4 more
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Genetic dosage compensation via co-occurrence of PMP22 duplication and PMP22 deletion
Neurology, 2015Charcot-Marie-Tooth disease type 1 A (CMT1A, OMIM #118220) and hereditary neuropathy with liability to pressure palsies (HNPP or tomaculous neuropathy, OMIM #162500) are autosomal dominantly inherited neuropathies caused by genomic rearrangements on chromosome 17p11.2-p12 containing PMP22 .
Hirt, Nina +7 more
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Dosage compensation of sex-linked genes in Drosophila melanogaster
Molecular and General Genetics MGG, 1973The phenomenon of dosage compensation in Drosophila melanogaster which consists in doubling of the activity of the X-chromosome genes in males as compared to those in females was studied.
L Z, Faizullin, V A, Gvozdev
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