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1.
Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair.
Cell
; 180(6): 1228-1244.e24, 2020 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32142649
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2.
Deep intronic founder mutations identified in the ERCC4/XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum.
Proc Natl Acad Sci U S A
; 120(27): e2217423120, 2023 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37364129
3.
TERT promoter mutations in thyroid cancer.
Endocr J
; 70(11): 1035-1049, 2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37532521
4.
[RET Gene Alterations in Thyroid Cancer-Towards Treatment with Selective RET Inhibitors].
Gan To Kagaku Ryoho
; 50(5): 611-614, 2023 May.
Artigo
em Japonês
| MEDLINE | ID: mdl-37218322
5.
Preoperative detection of the TERT promoter mutations in papillary thyroid carcinomas.
Clin Endocrinol (Oxf)
; 95(5): 790-799, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34322882
6.
Position paper from the Japan Thyroid Association task force on the management of low-risk papillary thyroid microcarcinoma (T1aN0M0) in adults.
Endocr J
; 68(7): 763-780, 2021 Jul 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33762511
7.
TERT promoter mutation in primary papillary thyroid carcinoma lesions predicts absent or lower 131 i uptake in metastases.
IUBMB Life
; 71(7): 1030-1040, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31026111
8.
Chromophobe renal cell carcinoma-like thyroid carcinoma: A novel clinicopathologic entity possibly associated with tuberous sclerosis complex.
Endocr J
; 64(9): 843-850, 2017 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28680002
9.
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.
Am J Hum Genet
; 92(5): 807-19, 2013 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23623389
10.
Association between p53-binding protein 1 expression and genomic instability in oncocytic follicular adenoma of the thyroid.
Endocr J
; 63(5): 457-67, 2016 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-26935218
11.
XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.
J Allergy Clin Immunol
; 136(4): 1007-17, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26255102
12.
Radiation signatures in childhood thyroid cancers after the Chernobyl accident: possible roles of radiation in carcinogenesis.
Cancer Sci
; 106(2): 127-33, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25483826
13.
Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome.
PLoS Genet
; 8(11): e1002945, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23144622
14.
Analysis of multiple markers for cancer stem-like cells in human thyroid carcinoma cell lines.
Endocr J
; 61(5): 481-90, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24531915
15.
Morphological difference in adult thyroid papillary carcinoma between Japan and Ukraine.
Endocr J
; 61(12): 1221-8, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25242260
16.
Radiation-Related Thyroid Cancer.
Endocr Rev
; 45(1): 1-29, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37450579
17.
TERT promoter mutations increase tumor aggressiveness by altering TERT mRNA splicing in papillary thyroid carcinoma.
J Clin Endocrinol Metab
; 2024 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38576411
18.
Functional characterization of the novel BRAF complex mutation, BRAF(V600delinsYM) , identified in papillary thyroid carcinoma.
Int J Cancer
; 132(3): 738-43, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22752848
19.
Significance of p53-binding protein 1 (53BP1) expression in thyroid papillary microcarcinoma: association with BRAFV600E mutation status.
Histopathology
; 63(5): 726-34, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24004175
20.
One-stage, simultaneous skin grafting with artificial dermis and basic fibroblast growth factor successfully improves elasticity with maturation of scar formation.
Wound Repair Regen
; 21(1): 141-54, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23228143