Detalhe da pesquisa
1.
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas.
Cell
; 167(5): 1264-1280.e18, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28084216
2.
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas.
Cell
; 174(5): 1325-1326, 2018 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30142346
3.
Whole-Genome Sequencing Identified New Structural Variations in the DMD Gene That Cause Duchenne Muscular Dystrophy in Two Girls.
Int J Mol Sci
; 24(17)2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37686372
4.
Genome-wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine-phosphate-guanine methylation and histological subtypes.
Genes Chromosomes Cancer
; 58(11): 783-797, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31334584
5.
Genetic and epigenetic changes in clonal descendants of irradiated human fibroblasts.
Exp Cell Res
; 370(2): 322-332, 2018 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29964050
6.
Dynamics of vertebrate sex chromosome evolution: from equal size to giants and dwarfs.
Chromosoma
; 125(3): 553-71, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26715206
7.
Chromosome Banding in Amphibia. XXXV. Highly Mobile Nucleolus Organizing Regions in Craugastor fitzingeri (Anura, Craugastoridae).
Cytogenet Genome Res
; 152(4): 180-193, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29059674
8.
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder.
J Child Psychol Psychiatry
; 58(7): 798-809, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28224622
9.
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.
Am J Hum Genet
; 92(5): 681-95, 2013 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23623388
10.
Sex chromosome polymorphism in guppies.
Chromosoma
; 123(4): 373-83, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24676866
11.
Co-Occurence of Reciprocal Translocation and COL2A1 Mutation in a Fetus with Severe Skeletal Dysplasia: Implications for Genetic Counseling.
Cytogenet Genome Res
; 145(1): 25-8, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25823796
12.
Non-syndromic hearing loss gene identification: A brief history and glimpse into the future.
Mol Cell Probes
; 29(5): 260-70, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25845345
13.
A Note from the New Editor.
Cytogenet Genome Res
; 158(2): 55, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31238325
14.
Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.
Genet Med
; 16(12): 945-53, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24875298
15.
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.
BMC Med Genet
; 15: 72, 2014 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24962056
16.
Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.
Am J Med Genet A
; 164A(2): 490-4, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24311106
17.
Roles of brca2 (fancd1) in oocyte nuclear architecture, gametogenesis, gonad tumors, and genome stability in zebrafish.
PLoS Genet
; 7(3): e1001357, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21483806
18.
Confirmation of GRHL2 as the gene for the DFNA28 locus.
Am J Med Genet A
; 161A(8): 2060-5, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23813623
19.
Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1.
Cells
; 12(12)2023 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37371073
20.
FancJ/Brip1 helicase protects against genomic losses and gains in vertebrate cells.
Genes Cells
; 16(6): 714-27, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21605288