Results 341 to 350 of about 1,530,143 (402)

Chromosome-specific aberrations, rather than general aneuploidy, may drive mouse embryonic stem cell-derived teratoma metastasis. [PDF]

Stem Cell Res Ther
Montilla-Rojo J, Hillenius S, Eleveld TF, Salvatori DCF, Looijenga LHJ.   +4 more
europepmc   +1 more source

Haplotype-resolved genome assembly of the tetraploid potato cultivar Désirée. [PDF]

Sci Data
Godec T, Beier S, Rodriguez-Granados NY, Sasidharan R, Abdelhakim L, Teige M, Usadel B, Gruden K, Petek M.   +8 more
europepmc   +1 more source

MicroFinder: Conserved gene-set mapping and assembly ordering for manual curation of bird microchromosomes

Mathers TC, Paulini M, Sotero-Caio CG, Wood JMD.   +3 more
europepmc   +1 more source

Identification of locally activated spindle-associated proteins in oocytes uncovers a phosphatase-driven mechanism

Wan X, Ohkura H.
europepmc   +1 more source

Genome evolution in parthenogenetic nematodes shaped by chromosome rearrangements and rare sex

Chung G, Stevens L, Dai X, Hickey S, Kiontke K, Rughani P, Kieninger MR, Collins JC, Juul S, Piano F, Fitch DHA, Blaxter M, Gunsalus KC.   +12 more
europepmc   +1 more source

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Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

Nature, 2008
Ludo Pagie, Wouter Meuleman, Lodewyk Fa Wessels   +2 more
exaly   +2 more sources

SMC complexes: from DNA to chromosomes

Nature Reviews Molecular Cell Biology, 2016
Frank Uhlmann
exaly   +2 more sources

Chromosomes. A comprehensive Xist interactome reveals cohesin repulsion and an RNA-directed chromosome conformation.

Science, 2015
The inactive X chromosome (Xi) serves as a model to understand gene silencing on a global scale. Here, we perform "identification of direct RNA interacting proteins" (iDRiP) to isolate a comprehensive protein interactome for Xist, an RNA required for Xi ...
Anand Minajigi, John E. Froberg, Chunyao Wei, Hongjae Sunwoo, Barry A. Kesner, David Colognori, D. Lessing, B. Payer, M. Boukhali, W. Haas, Jeannie T. Lee   +10 more
semanticscholar   +1 more source

Chromosome imprinting and the mammalian X chromosome [PDF]

Nature, 1975
Chromosome imprinting is the process by which one of two genetically homologous chromosomes is predetermined to function differently from the other at a subsequent stage in development. In the coccid insects, imprinting occurs in the egg, at the time of fertilisation; it probably occurs at the same time and site in mammals, and possibly also in Sciara.
Spencer W. Brown, H. Sharat Chandra
openaire   +2 more sources

Meiotic chromosomes: integrating structure and function.

Annual Review of Genetics, 1999
Meiotic chromosomes have been studied for many years, in part because of the fundamental life processes they represent, but also because meiosis involves the formation of homolog pairs, a feature which greatly facilitates the study of chromosome behavior.
D. Zickler, N. Kleckner
semanticscholar   +1 more source