Detalles de la búsqueda
1.
Increased SERPINB2 potentiates 15LO1 expression via STAT6 signalling in epithelial cells in eosinophilic chronic rhinosinusitis with nasal polyps.
Clin Exp Allergy
; 54(6): 412-424, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38639267
2.
Increased CYR61 expression activates CCND1/c-Myc pathway to promote nasal epithelial cells proliferation in chronic rhinosinusitis with nasal polyps.
Clin Immunol
; 247: 109235, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36681101
3.
Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosis.
Am J Obstet Gynecol
; 229(3): 302.e1-302.e18, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-36907537
4.
A Novel Splice Site Mutation in the FBN2 Gene in a Chinese Family with Congenital Contractural Arachnodactyly.
Biochem Genet
; 2023 Nov 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-37962692
5.
Pregnancy outcomes of rare autosomal trisomies results in non-invasive prenatal screening: clinical follow-up data from a single tertiary centre.
J Cell Mol Med
; 26(8): 2251-2258, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35174956
6.
Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency.
J Clin Lab Anal
; 36(12): e24786, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36441600
7.
[Prenatal diagnosis of fetuses with renal anomalies by whole genome sequencing].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(8): 819-823, 2022 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-35929929
8.
Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
BMC Med Genet
; 20(1): 180, 2019 11 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-31727011
9.
Identifying restoration priorities for wetlands based on historical distributions of biodiversity features and restoration suitability.
J Environ Manage
; 231: 1222-1231, 2019 Feb 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30602247
10.
Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case report.
BMC Med Genet
; 19(1): 61, 2018 04 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-29649982
11.
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.
Am J Obstet Gynecol
; 218(2): 244.e1-244.e17, 2018 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29128521
12.
[Genetic analysis and prenatal diagnosis for 25 Chinese pedigrees affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(6): 832-835, 2018 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-30512157
13.
[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(6): 853-856, 2017 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29188615
14.
Analysis of microbial differences in amniotic fluid between advanced and normal age pregnant women.
J Transl Med
; 19(1): 320, 2021 07 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-34315502
15.
[Detection of TSC1/TSC2 gene mutations among patients with tuberous sclerosis complex by Ion Torrent semiconductor sequencing].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(2): 169-72, 2016 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-27060308
16.
[Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(1): 11-5, 2014 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-24510553
17.
Noninvasive prenatal screening in a pregnant woman with a history of stem cell transplant from a male donor: A case report and literature review.
Mol Genet Genomic Med
; 12(6): e2479, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38860502
18.
Next-generation sequencing for genetic testing of hearing loss populations.
Clin Chim Acta
; 552: 117693, 2024 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38056549
19.
Insights from bioinformatics analysis reveal that lipopolysaccharide induces activation of chemokine-related signaling pathways in human nasal epithelial cells.
Sci Rep
; 14(1): 7672, 2024 04 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38561377
20.
PM2.5 activates IL-17 signaling pathway in human nasal mucosa-derived fibroblasts.
Int Immunopharmacol
; 128: 111484, 2024 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38199192