Results 21 to 30 of about 181,295 (168)
The calcium-sensing receptor (CaR) is a G-proteincoupled receptor that is widely expressed, has tissuespecific functions, regulates cell growth. Activating mutations of this receptor cause autosomal dominant hypocalcemia, a syndrome characterized by ...
Ana O. Hoff +5 more
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The ETS family of transcription factors is involved in several normal remodeling events and pathological processes including tumor progression. ETS transcription factors are divided into subfamilies based on the sequence and location of the ETS domain ...
Oorvashi Roy Puli +9 more
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The Inflammatory Pattern of Chronic Limb-Threatening Ischemia in Muscles: The TNF-α Hypothesis
Background: Vascular inflammation plays a crucial role in peripheral arterial disease (PAD), although the role of the mediators involved has not yet been properly defined.
Diego Caicedo +3 more
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SUMMARYThe development of multiple primary cancers (MPC) in the same individual is a rare clinical situation, although increasing in the last decades. The AA present a bibliographic review of this interesting subject.In the first part of the study they approach MPC in general. After a short historical perspective the classifications of Warren and Gates
M.a LuÃsa Soares De Oliveira +3 more
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Extranodal diffuse large B-cell lymphomas: A retrospective case series and review of the literature
Non-Hodgkin lymphomas commonly show extranodal involvement (25-30%) but primary diffuse large B-cell lymphomas(DLBCL) with extranodal localization represent clinically and molecularly distinct entities.
Stergios Boussios +8 more
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The RET tyrosine kinase receptor is expressed by the endocrine somatotroph cells of the pituitary where it has important functions regulating survival/apoptosis.
Alberto Pradilla Dieste +8 more
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Breast cancer and its therapies frequently result in significant musculoskeletal morbidity. Skeletal complications include bone metastases, pain, bone loss, osteoporosis, and fracture. In addition, muscle loss or weakness occurring in both the metastatic
Tarah J. Ballinger +2 more
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An aggressive and expanded phenotype in a kindred with a c.57delG SDHD mutation
Familial paraganglioma syndrome type 1 (PGL-1) is maternally imprinted, caused by SDHD mutations on the paternally inherited allele, and presents with paragangliomas and pheochromocytomas that are usually benign.
Celina Caetano +4 more
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Neoplasia and paracoccidioidomycosis [PDF]
Published studies on the association between cancer and paracoccidioidomycosis consist either isolated cases or clinical data based on hospital cohorts of paracoccidioidomycosis. The frequency of neoplasia in series of > or = 80 patients with paracoccidioidomycosis ranges from 0.16 to 14.1%, mean of 3.96%.
M A, Shikanai-Yasuda +5 more
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Em prosseguimento ao Programa de Atualização em Oncologia Pediátrica da Divisão Nacional de Câncer, foi realizado em Porto Alegre—RS, no período de 22 a 23 de abril de 1977, um Seminário de alto nível sobre Neuroblastoma, sob a coordenação local do Dr ...
Comissão Nacional de Neoplasia da Infância
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