نتایج جستجو برای: pheochromocytomas pccs

تعداد نتایج: 1151  

Journal: :Journal of Experimental & Clinical Cancer Research 2021

Abstract Background Pancreatic stellate cells (PSCs) occupy the majority of pancreatic cancer microenvironment, contributing to aggressive behavior (PCCs). Recently, anti-fibrotic agents have proven be an effective strategy against cancer, but clinical trials shown little efficacy, and driving mechanism remains unknown. N-acetyl-cysteine (NAC) is often used for pulmonary cystic fibrosis. Piogli...

Journal: :Cancer research 2000
D E Benn T Dwight A L Richardson L Delbridge C P Bambach M Stowasser R D Gordon D J Marsh B G Robinson

Pheochromocytomas are tumors of the adrenal medulla originating in the chromaffin cells derived from the neural crest. Ten % of these tumors are associated with the familial cancer syndromes multiple endocrine neoplasia type 2, von Hippel-Lindau disease (VHL), and rarely, neurofibromatosis type 1, in which germ-line mutations have been identified in RET, VHL, and NF1, respectively. In both the ...

Journal: :The Journal of clinical investigation 1991
S Khosla V M Patel I D Hay D J Schaid C S Grant J A van Heerden S N Thibodeau

Loss of heterozygosity (LOH) at specific loci may help localize tumor suppressor genes involved in the formation of various familial and sporadic tumors. In addition, the genetic loci for a number of familial tumor syndromes have been mapped by linkage analysis. To explore the possible role of tumor suppressor genes in endocrine tumors, we tested 41 pheochromocytomas (34 sporadic and 7 familial...

Journal: :Human molecular genetics 2012
Jenny Welander Catharina Larsson Martin Bäckdahl Niyaz Hareni Tobias Sivlér Michael Brauckhoff Peter Söderkvist Oliver Gimm

Pheochromocytomas are neuroendocrine tumors of the adrenal medulla which can occur either sporadically or in the context of hereditary tumor syndromes. Whereas the genetic background of hereditary pheochromocytomas is becoming rather well-defined, very little is known about the more common sporadic form of the disease which constitutes ∼70% of all cases. In this study, we elucidate some of the ...

2018
Henrik Falhammar Magnus Kjellman Jan Calissendorff

BACKGROUND With the increasing access to imaging more pheochromocytomas are diagnosed in the workup of adrenal incidentalomas. This may have changed the occurrence of the classic presentation with hypertension and the classic triad (headaches, sweating and palpitation). METHODS We reviewed 94 consecutive cases of pheochromocytomas. Two cases of ectopic ACTH-syndrome were subsequently excluded...

Journal: :Human molecular genetics 2011
Nelly Burnichon Laure Vescovo Laurence Amar Rossella Libé Aurélien de Reynies Annabelle Venisse Elodie Jouanno Ingrid Laurendeau Béatrice Parfait Jérôme Bertherat Pierre-François Plouin Xavier Jeunemaitre Judith Favier Anne-Paule Gimenez-Roqueplo

Pheochromocytomas and paragangliomas are neuroendocrine tumors that occur in the context of inherited cancer syndromes in ∼30% of cases and are linked to germline mutations in the VHL, RET, NF1, SDHA, SDHB, SDHC, SDHD, SDHAF2 and TMEM127 genes. Although genome-wide expression studies have revealed some of the mechanisms likely to be involved in pheochromocytoma/paraganglioma tumorigenesis, the ...

2014
Homero José de Farias e Melo Suzan M. Goldman Jacob Szejnfeld Juliano F. Faria Martha K. P. Huayllas Cássio Andreoni Cláudio E. Kater

OBJECTIVE To evaluate a protocol for two-dimensional (2D) hydrogen proton (1H) magnetic resonance spectroscopy (MRS) (Siemens Medical Systems; Erlangen, Germany) in the detection of adrenal nodules and differentiation between benign and malignant masses (adenomas, pheochromocytomas, carcinomas and metastases). MATERIALS AND METHODS A total of 118 patients (36 men; 82 women) (mean age: 57.3 ± ...

Journal: :Cancer research 1991
J F Moley M B Brother S A Wells B A Spengler J L Biedler G M Brodeur

Little is known about the prevalence and significance of ras gene activation in neural crest tumors such as neuroblastomas, pheochromocytomas, and medullary thyroid cancers (MTCs). Therefore, we analyzed DNA from 10 human neuroblastoma cell lines and 10 primary human pheochromocytomas for activating mutations in N-ras, H-ras, and K-ras. We also studied DNA from 24 primary neuroblastomas and 10 ...

Journal: :Rheumatology 2015
Fernando M Martins José António Pereira da Silva Maria José Santos Elsa Vieira-Sousa Cátia Duarte Helena Santos José António Costa Fernando M Pimentel-Santos Inês Cunha Luís Cunha Miranda Teresa Nóvoa Margarida Cruz Miguel Bernardes Domingos Araujo José Alberto Pereira Silva José Canas Silva Jaime Cunha Branco José António Melo Gomes Augusto Faustino João Eurico Fonseca Helena Canhão

OBJECTIVES . The 28-joint DAS (DAS28), clinical disease activity index (CDAI) and simplified disease activity index (SDAI) are indices frequently used to assess disease activity in RA patients. Cut-off values were defined to classify the states of RA disease activity: remission, low, moderate and high. The aim of this work was to assess disease activity states classified by DAS28, CDAI and SDAI...

2013
Vincent Busch Henk François Van Stel Johannes Rob Josephus De Leeuw Edward Melhuish Augustinus Jacobus Petrus Schrijvers

BACKGROUND In several countries centres for the integrated delivery of services to the parent and child have been established. In the Netherlands family health care service centres, called Parent and Child Centres (PCCs) involve multidisciplinary teams. Here doctors, nurses, midwives, maternity help professionals and educationists are integrated into multidisciplinary teams in neighbourhood-bas...

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