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1 sed 77 twin pregnancies, comprising complete hydatidiform mole (CHM) and healthy co-twin, to ascertai
6 nd sFlt-1 by ELISA in 17 women with complete hydatidiform mole (HM) and 20 gestational-age-matched no
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
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
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
23 istinguishable from an androgenetic complete hydatidiform mole, in which abnormal extra-embryonic tis
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
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
37 diagnosis, routine morphologic assessment of hydatidiform moles continues to suffer from interobserve
39 eotide polymorphism markers in most complete hydatidiform moles indicating that these tumors are not
41 iform moles and diandric triploid in partial hydatidiform moles) is a fundamental genetic event leadi