Detalhe da pesquisa
1.
Synthesis and activity of arylcoumarin derivatives with therapeutic effects on diabetic nephropathy.
Arch Pharm (Weinheim)
; 357(3): e2300524, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38036297
2.
Design, synthesis, and evaluation of dual-target inhibitors for the treatment of Alzheimer's disease.
Arch Pharm (Weinheim)
; 357(5): e2300693, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38332316
3.
Efficacy Analysis of Neoadjuvant versus Adjuvant Cisplatin-Paclitaxel Regimens for Initial Treatment of FIGO Stages IB3 and IIA2 Cervical Cancer.
Med Sci Monit
; 29: e940545, 2023 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38062672
4.
Genetic etiology and pregnancy outcomes of fetuses with central nervous system anomalies.
Arch Gynecol Obstet
; 2023 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37477678
5.
Fetus of 8q22.2q24.3 duplication and 13q33.2q34 deletion derived from a maternal balanced translocation.
J Obstet Gynaecol Res
; 46(9): 1900-1906, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32643293
6.
Genotype-phenotype correlations in a fetus with Kleefstra syndrome.
Taiwan J Obstet Gynecol
; 63(2): 238-241, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38485322
7.
Efficiency of copy number variation sequencing combined with karyotyping in fetuses with congenital heart disease and the following outcomes.
Mol Cytogenet
; 17(1): 12, 2024 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38741090
8.
DPAGT1-CDG: Recurrent fetal death.
Birth Defects Res
; 115(13): 1185-1191, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37421173
9.
Missed diagnosis of lissencephaly after prenatal diagnosis: A case report.
Medicine (Baltimore)
; 102(7): e33014, 2023 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36800618
10.
Genetic analysis and management of a familial hypercholesterolemia pedigree with polygenic variants: Case report.
Medicine (Baltimore)
; 102(32): e34534, 2023 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37565868
11.
A fetus of partial urorectal septum malformation sequence characterized by complete septate uterus: A case report.
Medicine (Baltimore)
; 102(13): e33448, 2023 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37000066
12.
45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome.
Case Rep Genet
; 2023: 9127512, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36938529
13.
Novel circular RNA circ-0002727 regulates miR-144-3p/KIF14 pathway to promote lung adenocarcinoma progression.
Front Cell Dev Biol
; 11: 1249174, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38033864
14.
Pregnancy outcomes and genetic analysis for fetal ventriculomegaly.
Front Genet
; 14: 1186660, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37795247
15.
An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12).
Clin Case Rep
; 10(7): e5984, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35846903
16.
A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report.
Medicine (Baltimore)
; 101(16): e29222, 2022 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35482990
17.
Caloric restriction induced epigenetic effects on aging.
Front Cell Dev Biol
; 10: 1079920, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36712965
18.
Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports.
Medicine (Baltimore)
; 101(43): e31321, 2022 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36316869
19.
Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype.
Mol Cytogenet
; 15(1): 48, 2022 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36329475
20.
A fetus with Bosch-Boonstra-Schaaf optic atrophy syndrome characterized by bilateral ventricle widening: A case report and related literature review.
Medicine (Baltimore)
; 101(40): e30558, 2022 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36221391