Detalhe da pesquisa
1.
Mitochondrial DNA variants segregate during human preimplantation development into genetically different cell lineages that are maintained postnatally.
Hum Mol Genet
; 31(21): 3629-3642, 2022 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35285472
2.
MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.
Hum Mol Genet
; 29(21): 3566-3577, 2021 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242073
3.
Association between sequence variants in the FSHR gene and reproductive outcomes following IVF in predicted normoresponders.
Reprod Biomed Online
; 46(5): 826-834, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37130623
4.
On the origins and fate of chromosomal abnormalities in human preimplantation embryos: an unsolved riddle.
Mol Hum Reprod
; 28(4)2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35404421
5.
CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.
Am J Hum Genet
; 100(3): 488-505, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28257691
6.
Human pluripotent stem cells in regenerative medicine: where do we stand?
Reproduction
; 156(5): R143-R153, 2018 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30325181
7.
Human embryonic stem cells show low-grade microsatellite instability.
Mol Hum Reprod
; 20(10): 981-9, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25082980
8.
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy.
Hum Reprod
; 29(8): 1603-9, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25006203
9.
Gains of 20q11.21 in human pluripotent stem cells: Insights from cancer research.
Stem Cell Reports
; 19(1): 11-27, 2024 01 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38157850
10.
SALL3 mediates the loss of neuroectodermal differentiation potential in human embryonic stem cells with chromosome 18q loss.
Stem Cell Reports
; 19(4): 562-578, 2024 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38552632
11.
Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweight.
Nat Commun
; 15(1): 1232, 2024 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38336715
12.
Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation.
Hum Mol Genet
; 20(1): 176-85, 2011 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20935170
13.
ISSCR standards for the use of human stem cells in basic research.
Stem Cell Reports
; 18(9): 1744-1752, 2023 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37703820
14.
Detecting mosaicism in trophectoderm biopsies.
Hum Reprod
; 32(3): 712-713, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28043945
15.
Measuring Early Germ-Layer Specification Bias in Human Pluripotent Stem Cells.
Methods Mol Biol
; 2429: 57-72, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35507155
16.
Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing.
Biol Open
; 11(1)2022 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35019138
17.
ESHRE survey results and good practice recommendations on managing chromosomal mosaicism.
Hum Reprod Open
; 2022(4): hoac044, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36349144
18.
The consequences of recurrent genetic and epigenetic variants in human pluripotent stem cells.
Cell Stem Cell
; 29(12): 1624-1636, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36459966
19.
The Impact of Acquired Genetic Abnormalities on the Clinical Translation of Human Pluripotent Stem Cells.
Cells
; 10(11)2021 11 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34831467
20.
Endogenous suppression of WNT signalling in human embryonic stem cells leads to low differentiation propensity towards definitive endoderm.
Sci Rep
; 11(1): 6137, 2021 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33731744