Detalhe da pesquisa
1.
Application of real-time PCR-based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses.
Ann Hum Genet
; 87(6): 316-325, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37771257
2.
TMEM63 mechanosensitive ion channels: Activation mechanisms, biological functions and human genetic disorders.
Biochem Biophys Res Commun
; 683: 149111, 2023 11 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37857161
3.
Molecular Determinants for the High-Affinity Blockade of Human Ether-à-go-go-Related Gene K + Channel by Tolterodine.
J Cardiovasc Pharmacol
; 80(5): 679-689, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35881423
4.
ß-Thalassemia Intermedia Caused by the ß-Globin Gene 3' Untranslated Region: Another Case Report.
Hemoglobin
; 46(2): 137-139, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35980111
5.
Severe Hb H Disease Caused by Hb Zürich-Albisrieden (HBA1: c.178G>C): Another Case Report.
Hemoglobin
; 46(6): 341-343, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36815319
6.
Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia.
Hemoglobin
; 44(3): 153-155, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32436451
7.
Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China.
Hemoglobin
; 44(2): 86-88, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32338097
8.
Coinheritance of Hb City of Hope (HBB: c.208G>A) and ß-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization.
Hemoglobin
; 43(2): 145-147, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31268351
9.
Results of Coexistence of ß-Thalassemia Minor in Hb H Disease Patients.
Hemoglobin
; 42(5-6): 306-309, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30614310
10.
Analysis of the Genotypes in a Chinese Population with Increased Hb A2 and Low Hematological Indices.
Hemoglobin
; 42(3): 154-158, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30277083
11.
KFL1 Gene Variants in α-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population.
Hemoglobin
; 42(3): 161-165, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30205725
12.
Chorioamnionitis and risk of long-term neurodevelopmental impairment in offspring.
Am J Obstet Gynecol
; 227(3): 548-549, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35430227
13.
First Report of the Rare IVS-II-705 (T>G) ß-Thalassemia Mutation in a Chinese Family.
Hemoglobin
; 41(4-6): 286-287, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29251008
14.
Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-ß-Thalassemia Trait.
Hemoglobin
; 41(4-6): 291-292, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29251016
15.
A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the ß-Globin Gene Leads to ß-Thalassemia.
Hemoglobin
; 41(1): 59-60, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28460555
16.
Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program.
Hemoglobin
; 41(4-6): 248-253, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29124982
17.
Upregulation of Transient Receptor Potential Canonical Channels Contributes to Endotoxin-Induced Pulmonary Arterial Stenosis.
Med Sci Monit
; 22: 2679-84, 2016 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27471122
18.
Mechanosensitive channels TMEM63A and TMEM63B mediate lung inflation-induced surfactant secretion.
J Clin Invest
; 134(5)2024 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38127458
19.
To Be or Not to Be an Ion Channel: Cryo-EM Structures Have a Say.
Cells
; 12(14)2023 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37508534
20.
Sphingosine-1-Phosphate Signaling in Cardiovascular Diseases.
Biomolecules
; 13(5)2023 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37238688