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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 ally demanding because mouse chromosomes are acrocentric and of similar size.
4 tric species polytypic for fission-generated acrocentric autosomes.
5 ted throughout centromeric regions of all 62 acrocentric autosomes.
6 ic two-thirds of dog chromosome 9 (CFA9), an acrocentric chromosome of medium size: P4HB, GALK1, TK1,
7                                       All 24 acrocentric chromosome sets of Xiphophorus are represent
8                        Rearrangements of the acrocentric chromosomes (Robertsonian translocations and
9 OBs are whole-arm rearrangements between the acrocentric chromosomes 13-15, 21, and 22.
10 nsidered, especially for cases involving the acrocentric chromosomes 14 and 15, in which UPD is assoc
11 mally located on the short arms (p11) of the acrocentric chromosomes and other heterochromatic region
12 including the pericentromeric regions of the acrocentric chromosomes and the heterochromatic portion
13 I (SatIII) DNA subfamilies cloned from human acrocentric chromosomes arose in the Hominoidea superfam
14 mensional preserved nuclei showed that human acrocentric chromosomes associate with hybrid cell nucle
15          Theoretically, a full complement of acrocentric chromosomes can be introduced into a populat
16  arm and one on the distal long arm, whereas acrocentric chromosomes exhibit a single site on the dis
17 tions of 1q10 to the short arms of different acrocentric chromosomes have also been identified, inclu
18 ial participation of the telomeres of the 15 acrocentric chromosomes in the Rabl configuration after
19 d and sequenced rDNA fragments from specific acrocentric chromosomes to (1) study homogenization alon
20 ned the nuclear location of individual human acrocentric chromosomes, and their associated NORs, in m
21 eats on 4q and those adjacent to rDNA on the acrocentric chromosomes, we investigated whether the FSH
22 se as a result of a telomeric fusion between acrocentric chromosomes, whereas chromosomes 4 and 19 in
23 oximal telomeres on the short arms of the 15 acrocentric chromosomes, which are apparently composed p
24 nes that are found on the short arm of human acrocentric chromosomes.
25 ric chromosome produced by the fusion of two acrocentric chromosomes.
26 ar organizer regions (NORs) on the p arms of acrocentric chromosomes.
27 DNA (rDNA) arrays on the short arms of human acrocentric chromosomes.
28  autosomal arms except the short arms of the acrocentric chromosomes.
29  autosomal arms except the short arms of the acrocentric chromosomes.
30 s 1 examined, although it also hybridized to acrocentric chromosomes.
31 or the most part in the satellite regions of acrocentric chromosomes.
32  genome, including the short arms of all the acrocentric chromosomes.
33 omosome arm, excluding the short arms of the acrocentric chromosomes.
34  metacentric chromosomes compared to smaller acrocentric chromosomes.
35 c chromosomes between centromere pairs forms acrocentric derivatives, (ii) de novo capping of newly s
36 t, relative to the corresponding segments of acrocentric dog chromosomes.
37 s, (ii) de novo capping of newly synthesized acrocentric ends with telomeric DNA stabilizes these der
38                 Chromosome 13 is the largest acrocentric human chromosome.
39 e HPV-8 E2 protein targets the short arms of acrocentric mitotic chromosomes.
40 otype, like that of the human and unlike the acrocentric mouse, has enabled us to demonstrate that th
41  uniparental disomy (UPD) associated with an acrocentric rearrangement, carriers are presumed to be a
42                   Four of the six homologous acrocentric rearrangements showed UPD, providing a risk
43         A total of 174 prenatally identified acrocentric rearrangements, including both Robertsonian
44 s Robertsonian translocations and homologous acrocentric rearrangements.
45 e submetacentric bovine X chromosome and the acrocentric sheep and goat X chromosomes.
46 Our results show that various regions of the acrocentric short arm, and, particularly, satellite III
47 eaks leading to their formation occur in the acrocentric short arm.
48 l repetitive DNA probes that localize to the acrocentric short arm.
49 hat are found within centromeric regions and acrocentric short arms.

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