Mendelian


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Related to Mendelian: Mendelian population
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a follower of Mendelism

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parent-of-origin or Mendelian QTL was performed according to the decision trees in Thomsen et al.
1] generations derived from crosses between homozygous tolerant transgenic Brassica napus lines and their susceptible parent cultivars and fit of observed segregations to Mendelian ratios.
Provided the presence or absence of the amplification product from a RAPD primer follows Mendelian transmission, they can be used to estimate the cytonuclear disequilibrium measure [D.
Contrary to Lysenko's intentions, his language gave his opponents, Soviet Mendelians, grounds on which to defend their science and criticize Lysenkoism.
However, since we think the causal substance is remnants, not actually triglycerides, we need a mendelian randomization study mapped to directly measured remnants.
2] increase in BMI, and in the Mendelian randomization cohort, the risk of gallstone disease increased 17% with every 1-kg/[m.
compile 56 chapters for all health professionals involved in the care of women with high-risk pregnancies that address such issues as nutrition, alcohol and substance abuse, and environmental agents and reproductive risk; genetic screening for Mendelian disorders and fetal aneuploidy and neural tube defects; monitoring fetal lung maturity, antepartum fetal monitoring, and interpreting intrapartum fetal heart tracings; and maternal diseases such as sickle cell anemia, cardiac disease, diabetes, asthma, epilepsy, hypertension, lupus, infections, hepatitis, and HIV.
Antonarakis of the University of Geneva lamented a decline in the number of new, single-gene diseases (that is, mendelian diseases) that were being described in the literature, compared with the growing number of research reports on the genetic basis of common, complex, and multigenic diseases.
Following maternal plasma DNA sequencing and relative haplotype dosage (RHDO) analysis was used to infer the mutational status of the fetus for inheritance of Mendelian disorders.
In this way, simple illustrations incorporate a considerable amount of information that provides the opportunity to determine genotype and phenotype probabilities for monogenic Mendelian traits without the need to draw Punnett square for every parental genotype combination.
Other articles discuss gene and variant annotation for Mendelian disorders in the era of advanced sequencing technologies; the yin and yang of autism genetics: how rare de novo and common variations affect liability; life as a clinical geneticist; charting the new terrain of precision prevention; participatory genomic research: ethical issues from the bottom up to the top Down; and application of panel-based tests for inherited risk of cancer.
By the 1930s, biologists had come to understand Darwin's gradualism as the net effect of contributions of countless separate, but individually very small, Mendelian effects.
Mycobacterial infections are observed commonly in patients with severe forms of primary immunodeficiency, including severe combined immune deficiency (SCID), complete Di George syndrome, X-linked hyper immunoglobulin (Ig)-M syndrome (HIGM type 1, CD154 deficiency), CD40 deficiency, immune deficiencies accompanying ectodermal dysplasia (nuclear factor kappa-beta essential modulator (NEMO), IKBA), chronic granulomatous disease (CGD), interleukin 12-interferon gamma (IL-12/IFN-[gamma]) receptor disorders, and hyper IgE syndrome, and these diseases have been examined under the title of Mendelian Susceptibility to Mycobacterial Diseases (MSMD) (3-12).
The condition affects one person in every 3,000 in the UK and is one of the world's most widespread mendelian genetic disorders.
The Mendelian spirit has dominated genetics since the middle of the twentieth century, especially the Human Genome Project and the production of full DNA sequences of many people.