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1 sed 77 twin pregnancies, comprising complete hydatidiform mole (CHM) and healthy co-twin, to ascertai
2 is based on the use of a homozygous complete hydatidiform mole (CHM) as the reference.
3  for alpha satellite containing reads in the hydatidiform mole (CHM1, haploid-like) genome.
4 g centromeric satellite arrays in a complete hydatidiform mole (CHM13).
5                          Familial biparental hydatidiform mole (FBHM) is the only known pure maternal
6 nd sFlt-1 by ELISA in 17 women with complete hydatidiform mole (HM) and 20 gestational-age-matched no
7                                              Hydatidiform mole (HM) is an abnormal gestation characte
8 eference-standard DNA mixtures of homozygote hydatidiform mole and heterozygote blood DNA at varying
9 , NLRP7 and NLRP2, cause familial biparental hydatidiform mole and multilocus imprinting disturbance,
10 e genome-wide restriction maps of a complete hydatidiform mole and three lymphoblast-derived cell lin
11 haliana, Drosophila melanogaster and a human hydatidiform mole cell line (CHM1) from SMRT sequencing.
12 read technologies, but it was derived from a hydatidiform mole cell line with a nearly homozygous gen
13 ong-read nanopore sequencing of the complete hydatidiform mole CHM13 genome, combined with complement
14        We used data generated from a haploid hydatidiform mole genome (CHM1) and a diploid human geno
15 development of the conceptus into a complete hydatidiform mole in which extraembryonic trophoblastic
16 t elevated LIGHT in the trophoblast cells of hydatidiform mole induces sFlt-1, which might underlie t
17           The most frequent type of complete hydatidiform mole is a 46, XX homozygote formed by the f
18                        We leverage a haploid hydatidiform mole to identify highly identical sequences
19 esent evidence of homozygosity of a complete hydatidiform mole using 20 diallelic markers distributed
20 emalignant disorders of complete and partial hydatidiform mole, and the malignant disorders of invasi
21 used genomic DNA from an essentially haploid hydatidiform mole, CHM1.
22 rations 6 months after uterine evacuation of hydatidiform mole, even when values are falling.
23 istinguishable from an androgenetic complete hydatidiform mole, in which abnormal extra-embryonic tis
24             These diseases vary from partial hydatidiform mole, which rarely metastasizes and infrequ
25 trations of hCG 6 months after evacuation of hydatidiform mole.
26  concentrations 6 months after evacuation of hydatidiform mole.
27                                     Complete hydatidiform moles (CHMs) are diploid tumors that result
28                     Rare familial biparental hydatidiform moles (due to NLRP7 or KHDC3L mutations) sh
29 entify novel genes responsible for recurrent hydatidiform moles (HMs), we performed exome sequencing
30 niparental tissues of germline origin, i.e., hydatidiform moles (paternal origin) and complete ovaria
31                                      Partial hydatidiform moles (PMs) rarely require chemotherapy and
32 sentation of the paternal genome in sporadic hydatidiform moles (purely androgenetic in complete hyda
33 iform moles (purely androgenetic in complete hydatidiform moles and diandric triploid in partial hyda
34 egnancy-related disorders, such as recurrent hydatidiform moles and fetal growth restriction, and thu
35                                              Hydatidiform moles are intriguing pathologic entities re
36                                              Hydatidiform moles are known to pose an extremely high r
37 diagnosis, routine morphologic assessment of hydatidiform moles continues to suffer from interobserve
38             76 (<1%) of 13,960 patients with hydatidiform moles had persistently high hCG concentrati
39 eotide polymorphism markers in most complete hydatidiform moles indicating that these tumors are not
40      The homozygous nature of these complete hydatidiform moles makes them unique resources for human
41 iform moles and diandric triploid in partial hydatidiform moles) is a fundamental genetic event leadi
42 orms are derived from the precursor lesions, hydatidiform moles.
43 hat these tumors are not related to complete hydatidiform moles.
44 nal-triploidy and the development of partial hydatidiform moles.
45 d to investigate the involvement of LIGHT in hydatidiform moles.
46 ostic methods for accurate classification of hydatidiform moles.