Detalhe da pesquisa
1.
Low oxygen enhances trophoblast column growth by potentiating differentiation of the extravillous lineage and promoting LOX activity.
Development
; 147(2)2020 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31871275
2.
Cell-specific characterization of the placental methylome.
BMC Genomics
; 22(1): 6, 2021 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33407091
3.
Genomic imbalances in the placenta are associated with poor fetal growth.
Mol Med
; 27(1): 3, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33413077
4.
Confined placental mosaicism involving multiple de novo copy number variants associated with fetal growth restriction: A case report.
Am J Med Genet A
; 185(6): 1908-1912, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33750025
5.
Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning.
Twin Res Hum Genet
; 24(3): 155-159, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34308812
6.
Mining DNA methylation alterations towards a classification of placental pathologies.
Hum Mol Genet
; 27(1): 135-146, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29092053
7.
The significance of the placental genome and methylome in fetal and maternal health.
Hum Genet
; 139(9): 1183-1196, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31555906
8.
Renpenning syndrome in a female.
Am J Med Genet A
; 182(3): 498-503, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31840929
9.
Review: placental biomarkers for assessing fetal health.
Hum Mol Genet
; 26(R2): R237-R245, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28595268
10.
Pervasive polymorphic imprinted methylation in the human placenta.
Genome Res
; 26(6): 756-67, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26769960
11.
Association of a placental Interleukin-6 genetic variant (rs1800796) with DNA methylation, gene expression and risk of acute chorioamnionitis.
BMC Med Genet
; 20(1): 36, 2019 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30795743
12.
Whole exome sequencing of families with 1q21.1 microdeletion or microduplication.
Am J Med Genet A
; 173(7): 1782-1791, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28475290
13.
Developmental transcription factor NFIB is a putative target of oncofetal miRNAs and is associated with tumour aggressiveness in lung adenocarcinoma.
J Pathol
; 240(2): 161-72, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27357447
14.
Cell-Free Placental DNA in Maternal Plasma in Relation to Placental Health and Function.
Fetal Diagn Ther
; 41(4): 258-264, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-27562338
15.
The human placenta methylome.
Proc Natl Acad Sci U S A
; 110(15): 6037-42, 2013 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-23530188
16.
Genome-wide DNA methylation identifies trophoblast invasion-related genes: Claudin-4 and Fucosyltransferase IV control mobility via altering matrix metalloproteinase activity.
Mol Hum Reprod
; 21(5): 452-65, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25697377
17.
Placental DNA methylation at term reflects maternal serum levels of INHA and FN1, but not PAPPA, early in pregnancy.
BMC Med Genet
; 16: 111, 2015 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26654447
18.
Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology.
Am J Med Genet A
; 167A(5): 1152-60, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25736541
19.
Noninvasive nucleic acid-based approaches to monitor placental health and predict pregnancy-related complications.
Am J Obstet Gynecol
; 213(4 Suppl): S197-206, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26428499
20.
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.
Hum Mutat
; 35(1): 58-62, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24130152