Detalhe da pesquisa
1.
Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans.
Mol Cell
; 80(6): 996-1012.e9, 2020 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33147438
2.
Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2.
Mol Cell
; 71(1): 25-41.e6, 2018 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29937342
3.
RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous Recombination.
Mol Cell
; 66(5): 622-634.e8, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28575658
4.
Meeting report: AT workshop 2023-A platform for discussing cutting-edge science in DNA damage signaling, repair, and human disorders.
Genes Cells
; 28(9): 642-645, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37341149
5.
The ribonuclease domain function is dispensable for SLFN11 to mediate cell fate decision during replication stress response.
Genes Cells
; 28(9): 663-673, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37469008
6.
SLFN11 promotes stalled fork degradation that underlies the phenotype in Fanconi anemia cells.
Blood
; 137(3): 336-348, 2021 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32735670
7.
Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency.
Blood
; 137(15): 2021-2032, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33512438
8.
Effects of the major formaldehyde catalyzer ADH5 on phenotypes of fanconi anemia zebrafish model.
Mol Biol Rep
; 50(10): 8385-8395, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37615925
9.
RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous Recombination.
Mol Cell
; 78(1): 192, 2020 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32243829
10.
[A new Fanconi anemia-like disorder, aldehyde degradation deficiency syndrome: two defense mechanisms working together for the genome and hematopoiesis].
Rinsho Ketsueki
; 64(7): 639-645, 2023.
Artigo
em Japonês
| MEDLINE | ID: mdl-37544724
11.
SMC5/6 acts jointly with Fanconi anemia factors to support DNA repair and genome stability.
EMBO Rep
; 21(2): e48222, 2020 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31867888
12.
Warsaw breakage syndrome DDX11 helicase acts jointly with RAD17 in the repair of bulky lesions and replication through abasic sites.
Proc Natl Acad Sci U S A
; 115(33): 8412-8417, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30061412
13.
[Aldehyde degradation deficiency (ADD) syndrome: discovery of a novel fanconi anemia-like inherited BMF syndrome due to combined ADH5/ALDH2 deficiency].
Rinsho Ketsueki
; 62(6): 547-553, 2021.
Artigo
em Japonês
| MEDLINE | ID: mdl-34219079
14.
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Hum Mutat
; 41(1): 122-128, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31513304
15.
Mcm8 and Mcm9 form a complex that functions in homologous recombination repair induced by DNA interstrand crosslinks.
Mol Cell
; 47(4): 511-22, 2012 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-22771115
16.
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.
Mol Cell
; 47(1): 61-75, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22705371
17.
Replication stress induces accumulation of FANCD2 at central region of large fragile genes.
Nucleic Acids Res
; 46(6): 2932-2944, 2018 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29394375
18.
Significance of 5-S-Cysteinyldopa as a Marker for Melanoma.
Int J Mol Sci
; 21(2)2020 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31936623
19.
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.
Haematologica
; 104(10): 1962-1973, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30792206
20.
Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia.
Ann Hematol
; 98(2): 271-280, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30368588