Detalhe da pesquisa
1.
CCL21-Ser expression in melanoma cells recruits CCR7+ naïve T cells to tumor tissues and promotes tumor growth.
Cancer Sci
; 114(9): 3509-3522, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37421165
2.
Interleukin-18 as a severity marker and novel potential therapeutic target for epidermolytic ichthyosis.
Clin Exp Dermatol
; 48(3): 199-210, 2023 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36656063
3.
A case of cutaneous syncytial myoepithelioma with extensive adipocytic metaplasia: Usefulness of EWSR1-PBX3 gene fusion analysis.
J Cutan Pathol
; 49(4): 412-417, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34854109
4.
CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells.
Proc Natl Acad Sci U S A
; 116(52): 26846-26852, 2019 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31818947
5.
Quantitative measurement of resistance force and subsequent attenuation during passive isokinetic extension of the wrist in patients with mild to moderate spasticity after stroke.
J Neuroeng Rehabil
; 19(1): 110, 2022 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36224659
6.
Possible relation of cathepsin C activity and seasonal fluctuation of skin lesions in Papillon-Lefèvre syndrome.
Br J Dermatol
; 190(2): 272-274, 2024 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37757845
7.
Mutations in SDR9C7 gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis.
Hum Mol Genet
; 25(20): 4484-4493, 2016 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28173123
8.
CADM1 is a diagnostic marker in early-stage mycosis fungoides: Multicenter study of 58 cases.
J Am Acad Dermatol
; 79(6): 1039-1046, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29928911
9.
Atypical epidermolytic palmoplantar keratoderma is a minimal phenotypic variant of epidermolytic ichthyosis: A new insight from ultrastructural findings.
J Eur Acad Dermatol Venereol
; 37(12): e1449-e1452, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37460199
10.
Pustular Skin Lesions in an Adult Female Patient with X-linked Dominant Chondrodysplasia Punctata with a Novel Emopamil Binding Protein Mutation: A Rare Skin Manifestation.
Acta Derm Venereol
; 101(9): adv00547, 2021 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34490468
11.
Late-onset Cutaneous Hydrophilic Polymer Embolism: A Case Occurring Two Years after Endovascular Procedures.
Acta Derm Venereol
; 101(7): adv00511, 2021 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34263328
12.
Alopecia areata and psoriasis vulgaris associated with Turner syndrome.
Australas J Dermatol
; 62(3): e453-e455, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34033128
13.
Refractory Bullous Pemphigoid Improved by Discontinuation of Phenytoin as an CYP3A4 Inducer.
Acta Derm Venereol
; 100(8): adv00108, 2020 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32215663
14.
Can dermatologists reach their full potential in teledermatology? A validation study of diagnostic performance of skin diseases in live video conferencing teledermatology.
J Dermatol
; 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38507330
15.
Two cases of infancy associated eosinophilic pustular folliculitis (I-EPF) comparing the profile of infiltrating cells with classic EPF by immunohistochemical study.
J Dermatol
; 51(1): 125-129, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37789597
16.
Inhibition of intracellular ATP synthesis impairs the recruitment of homologous recombination factors after ionizing radiation.
J Radiat Res
; 65(3): 263-271, 2024 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38461549
17.
Deep dermatophytosis caused by Trichophyton rubrum in an elderly patient with CARD9 deficiency: A case report and literature review.
J Dermatol
; 51(2): 294-300, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37804063
18.
Phylogenetic position and evolutionary history of the turtle and whale barnacles (Cirripedia: Balanomorpha: Coronuloidea).
Mol Phylogenet Evol
; 67(1): 9-14, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23306306
19.
Different degree of loss-of-function among four missense mutations in the EDAR gene responsible for autosomal recessive hypohidrotic ectodermal dysplasia may be associated with the phenotypic severity.
J Dermatol
; 50(3): 349-356, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36258277
20.
Endogenous CCL21-Ser deficiency reduces B16-F10 melanoma growth by enhanced antitumor immunity.
Heliyon
; 9(8): e19215, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37664721