Results 101 to 110 of about 27,666 (237)

On Technics and Technology as a Modification of the Death Drive

Constellations, EarlyView.
Lachlan Ross
wiley   +1 more source

Genomic and Transcriptomic Characterization of Protein Kinase C Fusion Melanocytic Neoplasms With Distinctive Hypopigmented Histomorphology: A Single‐Institution Study

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Background Genomic fusions involving Protein Kinase C (PKC or PRKC) have been classically identified in a subset of melanocytic neoplasms with heavy melanin pigmentation as described in older series. They were recently reclassified from the pigmented epithelioid melanocytoma (PEM) category to the blue nevus (BN) category in the fifth edition ...
Aofei Li, Brandon Umphress, Carina Dehner, Ryan Jones, Keller Toral, Simon Warren, Ahmed K. Alomari   +6 more
wiley   +1 more source

Optical super‐high magnification dermoscopy of benign and malignant melanocytic lesions in correlation with histopathology

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and objectives Technical advances have allowed for significant improvements in imaging techniques in recent years. Specifically, lesions can now be depicted at a much higher magnification – up to 400 x – using optical super‐high magnification dermoscopy (OSHMD).
Julia Katharina Winkler, Katharina Susanne Kommoss, Anastasia Sophie Vollmer, Alexander Heinrich Enk, Holger Andreas Haenssle, Ferdinand Toberer   +5 more
wiley   +1 more source

Editorial Comment on “Performance of PRAME immunohistochemistry compared with that of c‐Kit, c‐Myc, or cyclin D1 for the diagnosis of acral melanocytic tumors”

, 2023
Pathology International, Volume 73, Issue 1, Page 37-38, January 2023.
Miki Izumi
wiley   +1 more source

Rosacea in childhood and adolescence: A review

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Despite presenting with similar symptoms, triggers, and progression patterns as adults, rosacea in children and adolescents is frequently overlooked as a primary differential diagnosis. However, initial manifestations of classic clinical types can be observed from infancy onwards.
Sören Korsing, Karola Stieler, Uwe Pleyer, Ulrike Blume‐Peytavi, Annika Vogt   +4 more
wiley   +1 more source

The basal cell nevus syndrome.Disasters occurring among a series of 36 patients [PDF]

, 1979
Graeme Southwick, Robert A. Schwartz
openalex   +1 more source

An electron microscopic study of balloon cell nevus [PDF]

, 1972
Ken Hashimoto, George F. Bale
openalex   +1 more source

Y12C mutation disrupts IMPDH cytoophidia and alters cancer metabolism

The FEBS Journal, EarlyView.
IMPDH, the rate‐limiting enzyme for de novo GTP synthesis, can form polymers and cytoophidia to enhance activity by reducing GTP inhibition. In this study, a Y12C mutation in IMPDH2 was introduced via ABEmax base‐editing in human cancer cell lines to disrupt IMPDH polymerisation.
Chia‐Chun Chang, Min Peng, Gerson Dierley Keppeke, Li‐Kuang Tsai, Ziheng Zhang, Li‐Mei Pai, Li‐Ying Sung, Ji‐Long Liu   +7 more
wiley   +1 more source

Invasion of the brain by a cellular blue nevus of the scalp.A case report with light and electron microscopic studies [PDF]

, 1971
Gerald D. Silverberg, Marshall E. Kadin, Ronald F. Dorfman, John W. Hanbery, Donald J. Prolo   +4 more
openalex   +1 more source

Role of single‐nucleotide pleomorphism microarray in the classification of BAP1‐inactivated melanocytic tumours

Histopathology, EarlyView.
Here we report the features of 24 BAP1‐inactivated melanocytic tumours including 19 BAP1‐inactivated melanocytomas (BIMs) and five BAP1‐inactivated melanomas. BIMs have a favourable prognosis, even those with multiple copy number aberrations (CNAs).
Joseph S. Durgin, Nicholas A. Zoumberos, Taylor Novice, Douglas R. Fullen, Alexandra C. Hristov, Lori Lowe, Rajiv M. Patel, Paul W. Harms, Aleodor A. Andea, Scott C. Bresler   +9 more
wiley   +1 more source