Detalhe da pesquisa
1.
PlantPAN 4.0: updated database for identifying conserved non-coding sequences and exploring dynamic transcriptional regulation in plant promoters.
Nucleic Acids Res
; 52(D1): D1569-D1578, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37897338
2.
JustRNA: a database of plant long noncoding RNA expression profiles and functional network.
J Exp Bot
; 74(17): 4949-4958, 2023 09 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37523674
3.
Polypill and Combination Therapy: Blood Pressure and Cardiovascular Risk Reduction.
Curr Cardiol Rep
; 25(12): 1851-1858, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37991626
4.
Databases and prospects of dynamic gene regulation in eukaryotes: A mini review.
Comput Struct Biotechnol J
; 21: 2147-2159, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37013004
5.
The Prevalence and Risk Factors of Hypokalemia in Pregnancy-Related Hospitalizations: A Nationwide Population Study.
Int J Nephrol
; 2021: 9922245, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34258064
6.
Epidemiology and the Impact of Acute Kidney Injury on Outcomes in Patients with Rhabdomyolysis.
J Clin Med
; 10(9)2021 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34062839
7.
Novel Interleukin-10 Gene Polymorphism Is Linked to Gestational Diabetes in Taiwanese Population.
Front Genet
; 10: 89, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30873205
8.
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability.
Taiwan J Obstet Gynecol
; 57(4): 578-582, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30122582
9.
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
Taiwan J Obstet Gynecol
; 57(5): 730-733, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30342661
10.
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.
Taiwan J Obstet Gynecol
; 57(5): 734-738, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30342662
11.
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Taiwan J Obstet Gynecol
; 57(5): 739-744, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30342663
12.
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.
Taiwan J Obstet Gynecol
; 57(1): 128-132, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29458882
13.
Retrospective cause analysis of troponin I elevation in non-CAD patients: Special emphasis on sepsis.
Medicine (Baltimore)
; 96(37): e8027, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28906388
14.
Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome.
Taiwan J Obstet Gynecol
; 56(6): 840-842, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29241931
15.
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
Taiwan J Obstet Gynecol
; 56(4): 545-549, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28805616
16.
Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect.
Taiwan J Obstet Gynecol
; 56(4): 550-553, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28805617
17.
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.
Taiwan J Obstet Gynecol
; 56(2): 238-242, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28420516
18.
Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.
Taiwan J Obstet Gynecol
; 56(1): 102-105, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28254208
19.
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
Taiwan J Obstet Gynecol
; 56(6): 821-826, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29241927
20.
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
Taiwan J Obstet Gynecol
; 56(6): 836-839, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29241930