Results 181 to 190 of about 159,676 (211)
A genome-wide RNAi screen for novel CIN genes using human artificial chromosome. [PDF]
PNAS NexusLiskovykh M +13 more
europepmc +1 more source
Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen +13 more
wiley +1 more source
Reconstitution of DNA fragments on HAC/MAC via the fragment-assembly system. [PDF]
Sci RepSuzuki T +9 more
europepmc +1 more source
Microtubule depolymerization at kinetochores restricts anaphase spindle elongation. [PDF]
Nat Chem BiolChen GY +3 more
europepmc +1 more source
CENP-E initiates chromosome congression by opposing Aurora kinases to promote end-on attachments. [PDF]
Nat CommunVukušić K, Tolić IM.
europepmc +1 more source
XhetRel: a pipeline for X heterozygosity and relatedness analysis of sequencing data. [PDF]
Bioinform AdvSalman B, Bebek N, Uğur İşeri S.
europepmc +1 more source
Crossover interference mediates multiscale patterning along meiotic chromosomes. [PDF]
Nat CommunWhite MA +5 more
europepmc +1 more source
Optical genome mapping of a complex structural rearrangement family line on chromosome 18. [PDF]
HereditasCai L, Jiang Y, Zhang N, Chen X.
europepmc +1 more source