Detalhe da pesquisa
1.
Skin in the game: a review of single-cell and spatial transcriptomics in dermatological research.
Clin Chem Lab Med
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38656304
2.
The combined immunohistochemical expression of AMBRA1 and SQSTM1 identifies patients with poorly differentiated cutaneous squamous cell carcinoma at risk of metastasis: A proof of concept study.
J Cutan Pathol
; 51(6): 450-458, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38421158
3.
IL-8 correlates with nonresponse to neoadjuvant nivolumab in HPV positive HNSCC via a potential extracellular vesicle miR-146a mediated mechanism.
Mol Carcinog
; 62(9): 1428-1443, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37401875
4.
Understanding precancerous lesions of the oral cavity.
J Pathol
; 258(2): 103-105, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35894839
5.
Maintenance of chronicity signatures in fibroblasts isolated from recessive dystrophic epidermolysis bullosa chronic wound dressings under culture conditions.
Biol Res
; 56(1): 23, 2023 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37161592
6.
Omaveloxolone attenuates squamous cell carcinoma growth and disease severity in an Epidermolysis Bullosa mouse model.
Exp Dermatol
; 31(7): 1083-1088, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35285087
7.
Evaluating a Targeted Cancer Therapy Approach Mediated by RNA trans-Splicing In Vitro and in a Xenograft Model for Epidermolysis Bullosa-Associated Skin Cancer.
Int J Mol Sci
; 23(1)2022 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35008999
8.
Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.
Clin Chem
; 67(6): 876-888, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33969388
9.
Impaired Wound Healing, Fibrosis, and Cancer: The Paradigm of Recessive Dystrophic Epidermolysis Bullosa.
Int J Mol Sci
; 22(10)2021 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34065916
10.
Gentamicin B1 is a minor gentamicin component with major nonsense mutation suppression activity.
Proc Natl Acad Sci U S A
; 114(13): 3479-3484, 2017 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-28289221
11.
Desmoglein 2 modulates extracellular vesicle release from squamous cell carcinoma keratinocytes.
FASEB J
; 31(8): 3412-3424, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28438789
12.
Precision Medicine for Heritable Skin Diseases-The Paradigm of Epidermolysis Bullosa.
J Investig Dermatol Symp Proc
; 19(2): S74-S76, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30471755
13.
A novel KRT14 null mutation leads to autosomal recessive epidermolysis bullosa simplex.
Clin Exp Dermatol
; 48(4): 431-433, 2023 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36757906
14.
Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome.
Am J Hum Genet
; 95(3): 308-14, 2014 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25152456
15.
Neonatal imaging using an on-site small footprint MR scanner.
Pediatr Radiol
; 47(8): 1001-1011, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28470389
16.
Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.
Am J Hum Genet
; 93(2): 330-5, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23830519
17.
Type VII collagen regulates expression of OATP1B3, promotes front-to-rear polarity and increases structural organisation in 3D spheroid cultures of RDEB tumour keratinocytes.
J Cell Sci
; 127(Pt 4): 740-51, 2014 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24357722
18.
Novel CARD11 Mutations in Human Cutaneous Squamous Cell Carcinoma Lead to Aberrant NF-κB Regulation.
Am J Pathol
; 185(9): 2354-63, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26212909
19.
Sonographic markers associated with adverse neonatal outcomes among fetuses with gastroschisis: an 11-year, single-center review.
Am J Obstet Gynecol
; 214(2): 275.e1-275.e7, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26454131
20.
Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility.
Am J Hum Genet
; 91(6): 1115-21, 2012 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23176819