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1 osome significantly more frequently than the acrocentrics.
2 d the two shortest chromosomes (2 and 4) are acrocentric and carry NORs subterminally in their short
3 rangements, which led to transitions between acrocentric and metacentric chromosomes in both directio
4 ally demanding because mouse chromosomes are acrocentric and of similar size.
5 e detected two types of cervine X chromosome-acrocentric and submetacentric.
6 tions and subtelomeric, pericentromeric, and acrocentric areas.
7 tric species polytypic for fission-generated acrocentric autosomes.
8 ted throughout centromeric regions of all 62 acrocentric autosomes.
9 ic two-thirds of dog chromosome 9 (CFA9), an acrocentric chromosome of medium size: P4HB, GALK1, TK1,
10                                       All 24 acrocentric chromosome sets of Xiphophorus are represent
11 ly unresolved sequences, representing entire acrocentric chromosome short arms, gene family expansion
12 damage, and aneuploidy of an rDNA-containing acrocentric chromosome.
13                        Rearrangements of the acrocentric chromosomes (Robertsonian translocations and
14                  The short arms of the human acrocentric chromosomes 13, 14, 15, 21 and 22 (SAACs) sh
15 OBs are whole-arm rearrangements between the acrocentric chromosomes 13-15, 21, and 22.
16 nsidered, especially for cases involving the acrocentric chromosomes 14 and 15, in which UPD is assoc
17 uman genome, including the short arms of the acrocentric chromosomes and both sex chromosomes.
18 mally located on the short arms (p11) of the acrocentric chromosomes and other heterochromatic region
19 fic segmental duplications, centromeric DNA, acrocentric chromosomes and subterminal heterochromatin.
20 including the pericentromeric regions of the acrocentric chromosomes and the heterochromatic portion
21 I (SatIII) DNA subfamilies cloned from human acrocentric chromosomes arose in the Hominoidea superfam
22 mensional preserved nuclei showed that human acrocentric chromosomes associate with hybrid cell nucle
23          Theoretically, a full complement of acrocentric chromosomes can be introduced into a populat
24                            Here we show that acrocentric chromosomes contain pseudo-homologous region
25  arm and one on the distal long arm, whereas acrocentric chromosomes exhibit a single site on the dis
26 tions of 1q10 to the short arms of different acrocentric chromosomes have also been identified, inclu
27 appear nearly identical between heterologous acrocentric chromosomes in T2T-CHM13.
28 ial participation of the telomeres of the 15 acrocentric chromosomes in the Rabl configuration after
29 t within human nuclei, positioning of all 10 acrocentric chromosomes is dictated by nucleolar associa
30 ignals of recombination between heterologous acrocentric chromosomes seen in the HPRC draft pangenome
31 d and sequenced rDNA fragments from specific acrocentric chromosomes to (1) study homogenization alon
32 nfined to long chromosome arms, transforming acrocentric chromosomes to (sub)metacentric chromosomes.
33 ned the nuclear location of individual human acrocentric chromosomes, and their associated NORs, in m
34 duplications, and the short arms of all five acrocentric chromosomes, unlocking these complex regions
35 eats on 4q and those adjacent to rDNA on the acrocentric chromosomes, we investigated whether the FSH
36 se as a result of a telomeric fusion between acrocentric chromosomes, whereas chromosomes 4 and 19 in
37 oximal telomeres on the short arms of the 15 acrocentric chromosomes, which are apparently composed p
38 r organizing regions (NOR) of the five human acrocentric chromosomes, ~50% remain transcriptionally i
39 nes that are found on the short arm of human acrocentric chromosomes.
40  metacentric chromosomes compared to smaller acrocentric chromosomes.
41 ric chromosome produced by the fusion of two acrocentric chromosomes.
42 ar organizer regions (NORs) on the p arms of acrocentric chromosomes.
43 DNA (rDNA) arrays on the short arms of human acrocentric chromosomes.
44  autosomal arms except the short arms of the acrocentric chromosomes.
45  are located on the p-arms of the five human acrocentric chromosomes.
46  autosomal arms except the short arms of the acrocentric chromosomes.
47 s 1 examined, although it also hybridized to acrocentric chromosomes.
48 or the most part in the satellite regions of acrocentric chromosomes.
49  genome, including the short arms of all the acrocentric chromosomes.
50 omosome arm, excluding the short arms of the acrocentric chromosomes.
51 translocation (rob) results from fusion of 2 acrocentric chromosomes.
52 alignments, except in the centromeres of the acrocentric chromosomes.
53 e sequences, especially in the short arms of acrocentric chromosomes.
54 raph(5) constructed from centromere-spanning acrocentric contigs indicates the presence of regions in
55 c chromosomes between centromere pairs forms acrocentric derivatives, (ii) de novo capping of newly s
56 t, relative to the corresponding segments of acrocentric dog chromosomes.
57 s, (ii) de novo capping of newly synthesized acrocentric ends with telomeric DNA stabilizes these der
58                 Chromosome 13 is the largest acrocentric human chromosome.
59 e HPV-8 E2 protein targets the short arms of acrocentric mitotic chromosomes.
60 otype, like that of the human and unlike the acrocentric mouse, has enabled us to demonstrate that th
61 iety of chromosomal rearrangements involving acrocentric p-arms and observe silent, rDNA-containing N
62 ase, and found that nucleolar association of acrocentric p-arms can occur independently of rDNA conte
63          We demonstrate that a proportion of acrocentric p-arms in cell lines and from normal human d
64 reviously recalcitrant to sequencing such as acrocentric p-arms, ribosomal DNA arrays, and telomeric
65  uniparental disomy (UPD) associated with an acrocentric rearrangement, carriers are presumed to be a
66                   Four of the six homologous acrocentric rearrangements showed UPD, providing a risk
67         A total of 174 prenatally identified acrocentric rearrangements, including both Robertsonian
68 s Robertsonian translocations and homologous acrocentric rearrangements.
69 e submetacentric bovine X chromosome and the acrocentric sheep and goat X chromosomes.
70 Our results show that various regions of the acrocentric short arm, and, particularly, satellite III
71 eaks leading to their formation occur in the acrocentric short arm.
72 l repetitive DNA probes that localize to the acrocentric short arm.
73                                Excluding the acrocentric short arms and sex chromosomes, we identify
74 hat are found within centromeric regions and acrocentric short arms.
75                                          The acrocentric type is found in three independent deer line