Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Benjamin Korman"'
Autor:
Bo Shi, Wenxia Wang, Benjamin Korman, Li Kai, Qianqian Wang, Jun Wei, Swarna Bale, Roberta Goncalves Marangoni, Swati Bhattacharyya, Stephen Miller, Dan Xu, Mahzad Akbarpour, Paul Cheresh, Daniele Proccissi, Demirkan Gursel, Jair Machado Espindola-Netto, Claudia C.S. Chini, Guilherme C. de Oliveira, Johann E. Gudjonsson, Eduardo N. Chini, John Varga
Publikováno v:
iScience, Vol 24, Iss 1, Pp 101902- (2021)
Summary: The processes underlying synchronous multiple organ fibrosis in systemic sclerosis (SSc) remain poorly understood. Age-related pathologies are associated with organismal decline in nicotinamide adenine dinucleotide (NAD+) that is due to dysr
Externí odkaz:
https://doaj.org/article/0de8a21c584b46638ebb6231ab5a5a27
Autor:
Benjamin Korman, Roberta Goncalves Marangoni, Gabriel Lord, Jerrold Olefsky, Warren Tourtellotte, John Varga
Publikováno v:
Arthritis Research & Therapy, Vol 20, Iss 1, Pp 1-11 (2018)
Abstract Background A pivotal role for adipose tissue homeostasis in systemic sclerosis (SSc) skin fibrosis is increasingly recognized. The nuclear receptor PPAR-γ is the master regulator of adipogenesis. Peroxisome proliferator activated receptor-
Externí odkaz:
https://doaj.org/article/8a5a4e6e07f4466e8494b4eeadd3eca1
Autor:
Roberta G. Marangoni, Yuri Masui, Feng Fang, Benjamin Korman, Gabriel Lord, Junghwa Lee, Katja Lakota, Jun Wei, Philipp E. Scherer, Laszlo Otvos, Toshimasa Yamauchi, Naoto Kubota, Takashi Kadowaki, Yoshihide Asano, Shinichi Sato, Warren G. Tourtellotte, John Varga
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Skin fibrosis in systemic sclerosis (SSc) is accompanied by attrition of dermal white adipose tissue (dWAT) and reduced levels of circulating adiponectin. Since adiponectin has potent regulatory effects on fibroblasts, we sought to assess ad
Externí odkaz:
https://doaj.org/article/6f36cafe22ea4bf78193c98c31cf6636
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2016 (2016)
Introduction. Buschke-Ollendorf syndrome (BOS) is an uncommon syndrome characterized by osteopoikilosis and other bone abnormalities, accompanied by skin lesions, most frequently connective tissue nevi. BOS is caused by mutations in the LEMD3 gene, w
Externí odkaz:
https://doaj.org/article/81b2014aa90848899dde62602f774219
Autor:
Susan L Murphy, Yen T Chen, Yvonne C Lee, Mary Carns, Kathleen Aren, Benjamin Korman, Monique Hinchcliff, John Varga
Publikováno v:
Rheumatology. 62:SI64-SI73
Objectives Symptoms of people who have SSc are heterogeneous and difficult to address clinically. Because diverse symptoms often co-occur and may share common underlying mechanisms, identifying symptoms that cluster together may better target treatme
Autor:
Karen, Kruzer, Roberta, Goncalves Marangoni, Ilana, Heckler, Aya, Elhage, John, Varga, Monique, Hinchcliff, Mary, Carns, Kathleen, Aren, Amy, Wielgosz, Marc, Nuzzo, Iswariya, Venkataraman, Benjamin, Korman
Publikováno v:
J Clin Rheumatol
BACKGROUND/OBJECTIVES: The subset of ANA-positive patients with systemic sclerosis (SSc) who lack prototypic SSc-specific autoantibodies (centromere, topoisomerase, RNA polymerase III, “triple negative SSc”) is poorly characterized. We assessed c
Publikováno v:
Current Treatment Options in Rheumatology. 8:1-18
Autor:
Karen Kruzer, Benjamin Korman
Publikováno v:
Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases.
Publikováno v:
Journal of Leadership and Organizational Studies, 28(3), 306-321. SAGE Publishing
We investigated the turnover intentions of employees who perceive that they are being treated with more or less abusive supervision than their coworkers. We call this incongruent abusive supervision. Our findings support our theory that employees ass
Publikováno v:
Academy of Management Proceedings. 2022