Results 1 to 10 of about 79,198 (289)

RNA-Mediated Non-Mendelian Inheritance in Mice: The Power of Memory [PDF]

Biomolecules
The mouse genome is transcribed at different rates in both directions from the newly formed genome after fertilization. During embryonic genomic activation (EGA/ZGA), the first RNA metabolism creates heterogeneity between blastomeres.
Minoo Rassoulzadegan
doaj   +7 more sources

Assessing non-Mendelian inheritance in inherited axonopathies. [PDF]

Genet Med, 2020
Inherited axonopathies (IA) are rare, clinically and genetically heterogeneous diseases that lead to length-dependent degeneration of the long axons in central (hereditary spastic paraplegia [HSP]) and peripheral (Charcot-Marie-Tooth type 2 [CMT2]) nervous systems.
Bis-Brewer DM, Gan-Or Z, Sleiman P, Inherited Neuropathy Consortium, Hakonarson H, Fazal S, Courel S, Cintra V, Tao F, Estiar MA, Tarnopolsky M, Boycott KM, Yoon G, Suchowersky O, Dupré N, Cheng A, Lloyd TE, Rouleau G, Schüle R, Züchner S.   +19 more
europepmc   +9 more sources

Micromanipulation in Paramecium: From non-mendelian inheritance to the outlook for versatile micromachines. [PDF]

J Eukaryot Microbiol, 2022
Haga N.
europepmc   +3 more sources

Non-Mendelian Single-Nucleotide Polymorphism Inheritance and Atypical Meiotic Configurations are Prevalent in Hop

The Plant Genome, 2017
Hop ( L.) breeding programs seek to exploit genetic resources for bitter flavor, aroma, and disease resistance. However, these efforts have been thwarted by segregation distortion including female-biased sex ratios.
Dong Zhang, Katherine A. Easterling, Nicholi J. Pitra, Mark C. Coles, Edward S. Buckler, Hank W. Bass, Paul D. Matthews   +6 more
doaj   +2 more sources

The nucleoside diphosphate kinase gene Nme3 acts as quantitative trait locus promoting non-Mendelian inheritance. [PDF]

PLoS Genetics, 2012
The t-haplotype, a variant form of the t-complex region on mouse chromosome 17, acts as selfish genetic element and is transmitted at high frequencies (> 95%) from heterozygous (t/+) males to their offspring.
Hermann Bauer, Sabrina Schindler, Yves Charron, Jürgen Willert, Barica Kusecek, Bernhard G Herrmann   +5 more
doaj   +3 more sources

TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease. [PDF]

Hum Mutat, 2020
Chen W, Lin J, Wang L, Li X, Zhao S, Liu J, Akdemir ZC, Zhao Y, Du R, Ye Y, Song X, Zhang Y, Yan Z, Yang X, Lin M, Shen J, Wang S, Gao N, Yang Y, Liu Y, Li W, Liu J, Zhang N, Yang X, Xu Y, Zhang J, Delgado MR, Posey JE, Qiu G, Rios JJ, Liu P, Wise CA, Zhang F, Wu Z, Lupski JR, Wu N.   +35 more
europepmc   +3 more sources

Non-Mendelian inheritance patterns and extreme deviation rates of CGG repeats in autism. [PDF]

Genome Res, 2022
Annear DJ, Vandeweyer G, Sanchis-Juan A, Raymond FL, Kooy RF.   +4 more
europepmc   +3 more sources

RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens. [PDF]

Genes Genomics, 2022
Qiu M, Yu C, Zhu S, Liu S, Peng H, Xiong X, Chen J, Jiang X, Du H, Li Q, Zhang Z, Yang C.   +11 more
europepmc   +3 more sources

[SNG2], a prion form of Cut4/Apc1, confers non-Mendelian inheritance of heterochromatin silencing defect in fission yeast. [PDF]

Nucleic Acids Res
Sharma S, Srivastava S, Dubey RN, Mishra P, Singh J.   +4 more
europepmc   +2 more sources

Structural variants identified using non-Mendelian inheritance patterns advance the mechanistic understanding of autism spectrum disorder. [PDF]

HGG Adv, 2023
Kainer D, Templeton AR, Prates ET, Jacboson D, Allan ERO, Climer S, Garvin MR.   +6 more
europepmc   +2 more sources