Results 71 to 80 of about 17,734 (244)

Downregulation of β-catenin blocks fibrosis via Wnt2 signaling in human keloid fibroblasts

Tumor Biology, 2017
Keloid is a disorder of fibroproliferative diseases that occurs in wounds, characterized by an exaggerated response to injury. The key factor responsible for the disease process has not been identified.
Yumei Cai, Shize Zhu, Weiqun Yang, Mingmeng Pan, Chaoyang Wang, Wenyi Wu   +5 more
doaj   +1 more source

Endoscopic Total Thyroidectomy via a Single‐Port Subclavian Approach Versus Open Surgery for Papillary Thyroid Carcinoma

World Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Objective Historically, performing contralateral thyroid lobectomy and lymph node dissection via the subclavian approach has been considered challenging. This study evaluated the safety and feasibility of gasless endoscopic total thyroidectomy and central compartment neck dissection via the single‐port subclavian approach (SpSCA) in comparison
Pei‐Liang Lin, Fa‐Ya Liang, Lan‐Lan Deng, Ping Han, Ren‐Hui Chen, Xi‐Jun Lin, Jing‐Yi Wang, Xiao‐Ming Huang   +7 more
wiley   +1 more source

Characterization of the skin keloid microenvironment

, 2023
Keloids are a fibroproliferative skin disorder that develops in people of all ages. Keloids exhibit some cancer-like behaviors, with similar genetic and epigenetic modifications in the keloid microenvironment.
Hailong Chen, Huan Qian, Chen Wang, Mengwen Zhang   +3 more
core   +1 more source

Using bioinformatics approaches and experimental verification to identify HOXD8 as a key gene for keloid progression

Journal of Radiation Research and Applied Sciences
Background: Keloid is a cutaneous fibrotic disease characterized through excessive proliferation of fibrous tissue, which can induce scar swelling, pain and functional impairment. A full understanding of what causes keloid formation is still missing, and
Guizhen Xu, Huicai Wen, Hengyi Xu, Xing Li, Jianxiang Xiong, Jiaqi Wu, Ji Luo, Fen Fu   +7 more
doaj   +1 more source

Dystrophia Smolandiensis is characterized by a novel NQO1 variant and a distinct phenotype from COL17A1‐associated epithelial recurrent erosion dystrophy

Acta Ophthalmologica, EarlyView.
Abstract Purpose To determine the molecular cause of the two epithelial recurrent erosion dystrophies, Dystrophia Smolandiensis and Dystrophia Helsinglandica, and to identify phenotypic differences between the two conditions. Methods DNA samples and clinical data from structured interview records were obtained from the Swedish families in which ...
Karl De Geer, Kristina Lagerstedt‐Robinson, Daniel Nilsson, Cilla Söderhäll, Björn Hammar, Erik Björck   +5 more
wiley   +1 more source

KelS: Keloid Survey

, 2022
COMPARING WHAT THE PUBLIC IN DIFFERENT COUNTRIES KNOW ABOUT KELOID ...
Elizabeth Pitt, Guy Stanley, jonathon pleat, Diana Lim   +3 more
core   +1 more source

Robotic surgery for paediatric neurogenic lower urinary tract dysfunction: a systematic review

BJU International, Volume 135, Issue 4, Page 557-566, April 2025.
Objective To evaluate in a systematic review the outcomes, benefits, and limitations of robot‐assisted surgeries for paediatric neurogenic lower urinary tract dysfunction (LUTD), as robot‐assisted techniques have emerged as a potential alternative, offering enhanced precision, dexterity, and visualisation.
Ihtisham Ahmad, Dheidan Alshammari, Priyank Yadav, Michael Chua, Margarita Chancy, Mohd S. Ansari, Mohan S. Gundeti   +6 more
wiley   +1 more source

Keloid pathophysiology: fibroblast or inflammatory disorders? [PDF]

, 2019
BackgroundKeloids are defined as a benign dermal fibroproliferative disorder with no malignant potential. They tend to occur following trivial trauma or any form of trauma in genetically predisposed individuals.
Nangole, Ferdinand W, Agak, George W
core   +1 more source

Pink Polypoid Papulo‐Vesicles on Labia Majora

JEADV Clinical Practice, EarlyView.
Maria Chiara Mercuri, Michela Tabanelli, Silvia Zago, Diego Abbenante   +3 more
wiley   +1 more source

Solitary Indeterminate Cell Histiocytosis Presenting as a Reddish Nodule on the Abdomen of a 4‐Year‐Old Boy: Clinicopathologic Correlation and Electron Microscopy Findings

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Indeterminate cell histiocytosis (ICH) is a clonal proliferative disorder of mononuclear phagocyte cells that shows features of both dendritic and histiocytic cells. Only around 100 cases of ICH were reported, and among them, only 24% of reported cases involve pediatric patients, with a mean age at diagnosis of 50 years.
Seung‐Soo Lee, Seok‐Jong Lee, Weon Ju Lee, Dae‐Lyong Ha   +3 more
wiley   +1 more source