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1 es implicates MCV as an etiological agent of Merkel cell carcinoma.
2 eted neurological disorder in the setting of Merkel cell carcinoma.
3 squamous cell carcinoma, Kaposi sarcoma, and Merkel cell carcinoma.
4 e for unresectable, recurrent, or metastatic Merkel cell carcinoma.
5 2016 was conducted among 3720 patients with Merkel cell carcinoma.
6 Incidence rates of Merkel cell carcinoma.
7 tal risk factor and prognostic biomarker for Merkel cell carcinoma.
8 rcinoma, basal cell carcinoma, melanoma, and Merkel cell carcinoma.
9 and salvage therapeutic option for advanced Merkel cell carcinoma.
10 ephalopathy (PML), BK virus nephropathy, and Merkel cell carcinoma.
11 nitors are and whether they can give rise to Merkel cell carcinoma.
12 epresent a potential therapeutic approach in Merkel cell carcinoma.
13 esents a new therapeutic option for advanced Merkel cell carcinoma.
14 tient for prostate cancer, and 1 patient for Merkel cell carcinoma.
15 either melanoma, squamous cell carcinoma, or Merkel cell carcinoma.
16 n polyomavirus causing the majority of human Merkel cell carcinomas.
17 mavirus (MCPyV), the causative agent of most Merkel cell carcinomas.
18 cently described as the cause for most human Merkel cell carcinomas.
20 n cancer, including melanoma (3419 [89.1%]), Merkel cell carcinoma (121 [3.2%]), hemangiosarcoma (104
21 st common cancer (1471 [61.8%]), followed by Merkel cell carcinoma (334 [14.0%]), Kaposi sarcoma (186
22 nts), squamous cell carcinoma (26 patients), Merkel cell carcinoma (6 patients), pigmented epithelioi
24 stage (unresectable, recurrent, or stage IV) Merkel cell carcinoma, a minimum of two tumour lesions m
25 regeneration is of interest to the study of Merkel cell carcinoma, a rare neuroendocrine skin cancer
26 viral T antigens is a common feature of most Merkel cell carcinomas, a primary neuroendocrine skin tu
27 therapy-refractory, histologically confirmed Merkel cell carcinoma (aged >/=18 years) were enrolled f
28 avirus Merkel cell polyomavirus (MCV) causes Merkel cell carcinoma, an aggressive but rare human skin
30 rus (MCPyV) was identified recently in human Merkel cell carcinomas, an aggressive neuroendocrine ski
31 DG PET may be a useful technique for staging Merkel cell carcinoma and for assessing the tumor respon
34 ceptor repertoire associated with 72 primary Merkel cell carcinomas and correlated metrics of the T-c
37 adiotherapy (SBRT) in patients with advanced Merkel cell carcinoma as a first-line therapy or followi
38 ons resembling clonally expanded variants in Merkel cell carcinomas, as well as novel junctions betwe
39 made in the study of human papillomaviruses, Merkel cell carcinoma-associated polyomavirus, Epstein-B
42 le and female mouse sensory neurons, a human Merkel cell carcinoma cell line and female human iPSC-de
48 d in the USA for the treatment of metastatic Merkel cell carcinoma, has shown antitumour activity and
49 aneous squamous cell carcinoma, melanoma, or Merkel cell carcinoma if surgery and/or radiotherapy hav
50 ojected that there will be 3023 new cases of Merkel cell carcinoma in 2020 and 5130 new cases in 2030
52 e period from 2012 to 2016, the age-adjusted Merkel cell carcinoma incidence rate was 0.66 per 100 00
64 lthough the causative link between MCPyV and Merkel cell carcinoma is well established, the molecular
66 cinoma (SCC) and rare skin tumors, including Merkel cell carcinoma (MCC) and dermatofibrosarcoma prot
68 ator of Merkel cell development, its role in Merkel cell carcinoma (MCC) carcinogenesis remains contr
70 le has been done to characterize how closely Merkel cell carcinoma (MCC) cell lines model native tumo
71 ncoprotein that drives the transformation of Merkel cell carcinoma (MCC) cells by activating transcri
72 the size of local excision (LE) margins for Merkel cell carcinoma (MCC) have not been well establish
73 ous cell carcinoma (SCC), melanoma (MM), and Merkel cell carcinoma (MCC) in a cohort of US OTRs recei
128 imary cancers after a diagnosis of cutaneous Merkel cell carcinoma (MCC) is not well established.
129 targeted therapeutic intervention.IMPORTANCE Merkel cell carcinoma (MCC) is the most aggressive cutan
137 avirus (MCPyV) is frequently associated with Merkel cell carcinoma (MCC), a highly aggressive neuroen
138 Merkel cell polyomavirus (MCPyV) can lead to Merkel cell carcinoma (MCC), a lethal form of skin cance
139 study, we investigated the susceptibility of Merkel cell carcinoma (MCC), a neuroendocrine carcinoma
140 rkel cell polyomavirus (MCPyV), was found in Merkel cell carcinoma (MCC), a rare aggressive skin canc
141 n polyomavirus etiologically associated with Merkel cell carcinoma (MCC), a rare and aggressive form
143 to be clonally integrated in 80% of cases of Merkel cell carcinoma (MCC), a rare but aggressive form
144 or clinical applications of such pathways in Merkel cell carcinoma (MCC), a rare but lethal cutaneous
145 ncy is perturbed, the virus can give rise to Merkel cell carcinoma (MCC), an aggressive and difficult
146 as been associated with approximately 80% of Merkel cell carcinoma (MCC), an aggressive and increasin
147 irus (MCPyV) causes the majority of cases of Merkel cell carcinoma (MCC), an aggressive skin cancer w
148 ed to support the etiologic role of MCPyV in Merkel cell carcinoma (MCC), an extremely lethal form of
149 l polyomavirus (MCPyV) in the development of Merkel cell carcinoma (MCC), making MCPyV the first poly
150 skin tumors, basal cell carcinoma (BCC) and Merkel cell carcinoma (MCC), with overlapping histologic
151 he biophysical properties of piezo2 in human Merkel cell carcinoma (MCC)-13 cells; piezo2 is a low-th
166 ting conclusions regarding the proportion of Merkel cell carcinomas (MCCs) that contain the Merkel ce
168 ered in 2008, drives the development of most Merkel cell carcinomas (MCCs) through several canonical
169 MCV) contributes to approximately 80% of all Merkel cell carcinomas (MCCs), a highly aggressive neuro
170 CV) is the recently discovered cause of most Merkel cell carcinomas (MCCs), an aggressive form of non
174 progressive multifocal leukoencephalopathy, Merkel cell carcinoma, pruritic rash or trichodysplasia
175 e recently been discovered: MCV was found in Merkel cell carcinoma samples, while Karolinska Institut
177 mab and ipilimumab in patients with advanced Merkel cell carcinoma showed a high ORR with durable res
178 posi sarcoma (SIR, 20.5; 95% CI, 17.7-23.7), Merkel cell carcinoma (SIR, 16.2; 95% CI, 14.5-18.1), an
179 -associated T cells correlates with improved Merkel cell carcinoma-specific survival, but the prognos
180 association with Kaposi sarcoma and include Merkel cell carcinoma, squamous cell carcinoma, and high
181 9, 95% confidence interval = 3.13-8.11), and Merkel cell carcinoma (standardized incidence ratio = 3.
182 noclonal antibody, in patients with stage IV Merkel cell carcinoma that had progressed after cytotoxi
183 MCV) causes an aggressive human skin cancer, Merkel cell carcinoma, through expression of small T (sT
184 that the 81% of patients with virus-positive Merkel cell carcinoma tumors had earlier stage disease a
185 has been shown to be the etiologic cause of Merkel cell carcinoma, understanding the mechanisms by w
187 ons; however, the spicules were positive for Merkel cell carcinoma virus, which is also a polyomaviru
188 t part of the initial increased incidence of Merkel cell carcinoma was associated with increased dete
189 yV-induced cellular proliferation.IMPORTANCE Merkel cell carcinoma was first described in 1972 as a n
190 idence for diffuse large B-cell lymphoma and Merkel cell carcinoma was observed only among people liv
191 with pembrolizumab in patients with advanced Merkel-cell carcinoma was associated with an objective r
192 ell neuroendocrine malignancies, 14 cases of Merkel cell carcinoma were analyzed by reverse transcrip
194 lled study, we assigned adults with advanced Merkel-cell carcinoma who had received no previous syste