Results 181 to 190 of about 1,311,035 (215)

Whole genome uniparental isodisomy detected using single nucleotide polymorphism (SNP) microarray in molar pregnancy: a case report. [PDF]

Mol Cytogenet
Okonkwo OO, Ortega V, Kane S, Aldrete G, Ramirez P, Valente PT, Velagaleti GVN.   +6 more
europepmc   +1 more source

A human induced pluripotent stem cell toolbox for studying sex chromosome effects

Meleckyte R, Varsally W, Zohren J, Eriksson J, Incitti T, Starnes L, Pointon A, Hicks R, Powell BE, Turner JM.   +9 more
europepmc   +1 more source

An Incidental Finding of Gain of a Diminished Chromosome 12 Centromere in an Individual with Lymphocytosis: A Case Report and Clinical Implications in Cytogenetic Testing. [PDF]

Diagnostics (Basel)
Xia C, Cannatella JJ, Smith SC, Althof PA, Koerselman H, Hempel T, Jaworski EE, Winkler LM, Spaulding JR, Pickering D, Khoury JD, Tang Z.   +11 more
europepmc   +1 more source

Case report: Clinical and genetic features of pediatric choroidal melanoma. [PDF]

Front Med (Lausanne)
Valente P, Galardi A, Di Giannatale A, Romanzo A, Novelli A, Orlando V, Colletti M, Russo I, De Vito R, Iarossi G, Petroni S, Sinibaldi L, Buzzonetti L.   +12 more
europepmc   +1 more source

Efficient blockLASSO for polygenic scores with applications to all of us and UK Biobank. [PDF]

BMC Genomics
Raben TG, Lello L, Widen E, Hsu SDH.
europepmc   +1 more source

High variability in chromosome number from a clade within the gourami family (Teleostei, Osphronemidae). [PDF]

Comp Cytogenet
Mobley B, Anderson AP.
europepmc   +1 more source

Chromosome segregation dynamics during the cell cycle ofStaphylococcus aureus

Izquierdo-Martinez A, Schäper S, Brito AD, Liao Q, Tesseur C, Sorg M, Botinas DS, Wang X, Pinho MG.   +8 more
europepmc   +1 more source

A Universal Scaling Law for Mitotic Spindles Driven by Chromosome Crowding

Gudlin L, Vukušić K, Novak M, Trupinić M, Ljulj M, Dundović I, Petelinec A, Petrušić L, Hertel A, van Ravesteyn T, Trakala M, Kops GJPL, Storchová Z, Tambača J, Pavin N, Tolić IM.   +15 more
europepmc   +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
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Chromosomal Instability

Current Opinion in Oncology, 2004
This review discusses numerical and structural chromosomal instability in cancer cells and its possible etiologies, highlighting the recent literature.Defects in chromosomal segregation, telomere stability, and the DNA damage response play significant roles in chromosomal instability in cancer.The pace of discoveries into the biologic basis of ...
openaire   +2 more sources