Detalhe da pesquisa
1.
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets.
Clin Endocrinol (Oxf)
; 87(1): 103-112, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28383812
2.
IL-12 immunotherapy of Braf(V600E)-induced papillary thyroid cancer in a mouse model.
Lab Invest
; 96(1): 89-97, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26501867
3.
KRAS(G12D)-mediated oncogenic transformation of thyroid follicular cells requires long-term TSH stimulation and is regulated by SPRY1.
Lab Invest
; 95(11): 1269-77, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26146959
4.
Increased CYP24A1 expression is associated with BRAF(V600E) mutation and advanced stages in papillary thyroid carcinoma.
Clin Endocrinol (Oxf)
; 81(1): 109-16, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24382015
5.
Molecular characterization of a novel p.R118C mutation in the insulin receptor gene from patients with severe insulin resistance.
Clin Endocrinol (Oxf)
; 76(4): 540-7, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22017372
6.
A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype.
Clin Endocrinol (Oxf)
; 75(6): 791-800, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21627674
7.
Clonal architecture in mesothelioma is prognostic and shapes the tumour microenvironment.
Nat Commun
; 12(1): 1751, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33741915
8.
Aberrant BRAF splicing as an alternative mechanism for oncogenic B-Raf activation in thyroid carcinoma.
J Pathol
; 217(5): 707-15, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19156774
9.
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.
J Clin Endocrinol Metab
; 103(5): 1889-1898, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29546359
10.
Cyp24a1 Attenuation Limits Progression of BrafV600E -Induced Papillary Thyroid Cancer Cells and Sensitizes Them to BRAFV600E Inhibitor PLX4720.
Cancer Res
; 77(8): 2161-2172, 2017 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28242615
11.
Clinical case seminar: metastatic follicular thyroid carcinoma arising from congenital goiter as a result of a novel splice donor site mutation in the thyroglobulin gene.
J Clin Endocrinol Metab
; 91(3): 740-6, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16403815
12.
Ribonucleic acid interference targeting S100A4 (Mts1) suppresses tumor growth and metastasis of anaplastic thyroid carcinoma in a mouse model.
J Clin Endocrinol Metab
; 91(6): 2373-9, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16551737
13.
Author Correction: Clonal architecture in mesothelioma is prognostic and shapes the tumour microenvironment.
Nat Commun
; 12(1): 3569, 2021 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34099722
14.
Mesothelioma: Hippo pathway as a target, lessons from COMMAND.
Oncotarget
; 10(40): 3996-3997, 2019 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31976036
15.
Concomitant RAS, RET/PTC, or BRAF mutations in advanced stage of papillary thyroid carcinoma.
Thyroid
; 24(8): 1256-66, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24798740
16.
Novel and de novo PHEX mutations in patients with hypophosphatemic rickets.
Bone
; 52(1): 286-91, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23079138
17.
Mutation prediction by PolyPhen or functional assay, a detailed comparison of CYP27B1 missense mutations.
Endocrine
; 40(1): 14-20, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21604088
18.
A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1.
J Clin Endocrinol Metab
; 95(9): 4176-83, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20534770
19.
Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinoma.
J Clin Endocrinol Metab
; 95(3): 1000-6, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20089614
20.
Oncogenic activation of MAP kinase by BRAF pseudogene in thyroid tumors.
Neoplasia
; 11(1): 57-65, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19107232