Detalhe da pesquisa
1.
Cell-type specialization is encoded by specific chromatin topologies.
Nature
; 599(7886): 684-691, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34789882
2.
Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestes.
Development
; 150(17)2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37519269
3.
Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice.
Genome Res
; 26(2): 183-91, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26755636
4.
Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction.
J Med Genet
; 54(11): 754-761, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28779001
5.
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.
Am J Hum Genet
; 95(6): 763-70, 2014 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25480037
6.
The dynamics of chromatin architecture in brain development and function.
Curr Opin Genet Dev
; 67: 84-93, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33421764
7.
Evolving methodologies and concepts in 4D nucleome research.
Curr Opin Cell Biol
; 64: 105-111, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32473574
8.
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality.
Science
; 370(6513): 208-214, 2020 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33033216
9.
Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesis.
Nat Genet
; 50(10): 1463-1473, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30262816
10.
Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice.
Cell Rep
; 10(5): 833-839, 2015 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25660031