Search Results for model

..., positive with TLE1 and SS18-SSX, and lack a CD34 and STAT6 reaction ( 296 , 482 ). Treatment and Prognosis. There are several multivariable risk stratification models for prognostication ( 454 , 458 , 483 , 484 ), although they are not optimized for the relatively smaller size of sinonasal tract tumors...

... . Joint effects of intensity and duration of cigarette smoking on the risk of head and neck cancer: a bivariate spline model approach . Oral Oncol   2019 ; 94 : 47 - 57 . 15. Ghantous   Y , Schussel   JL , Brait   M . Tobacco and alcohol-induced epigenetic changes in oral carcinoma...

..., vertebral anomalies such as hemivertebrae, fusion or elongation of the vertebral bodies, modeling defects of the hands and feet  Cleft lip or palate, polydactyly  Cardiac or ovarian fibroma  Medulloblastoma  Other skeletal abnormalities: Sprengel deformity, marked pectus deformity, marked...

... in primary melanomas . J Natl Cancer Inst   2003 ; 95 : 1878 - 90 . 298. Greenwald   HS , Friedman   EB , Osman   I . Superficial spreading and nodular melanoma are distinct biological entities: a challenge to the linear progression model . Melanoma Res   2012 ; 22 : 1 - 8 . 299...

... carbohydrate scaffold for vocal fold medialization in an ovine model . OTO Open   2023 ; 7 : e69 . 45. Yeretsian   RA , Blodgett   TM , Branstetter   BF   4th , Roberts   MM , Meltzer   CC . Teflon-induced granuloma: a false-positive finding with PET resolved with combined PET and CT...

... in ARMC5-mutant in vitro models is, however, in contrast to the association between ARMC5-inactivating mutations and higher cortisol levels in patients. The relative inefficiency to produce cortisol in ARMC5-mutated cells is probably compensated by the larger adrenal mass observed...

... ). An integrated model for malignancy risk assessment based on tumor size and tumor-to-liver uptake SUV_max ratio has been proposed recently to calculate an individual malignancy risk for a patient-based decision-making process ( 98 ). Currently, the American College of Radiology committee on incidental...

... techniques and mathematical models have been proposed for differentiating these lesions ( 99 ). Pathology Pitfalls and Common Differential Diagnoses As with primary adrenal tumors, adrenal metastases are increasingly recognized during life with the aid of high-resolution imaging studies such as CT scan...

... emerging from the intermediolateral column (IML) of the spinal cord. They then travel to the developing adrenal glands (AG) guided by those axons, which will also provide innervation of the medulla (DA = dorsal aorta). (Courtesy of Drs. M. Kastriti and I. Adameyko, Vienna, Austria) This model may help...

... Pharmacol   2012 ; 70 : 477 - 86 . 100. Iyer   R , Wehrmann   L , Golden   RL , et al . Entrectinib is a potent inhibitor of Trk-driven neuroblastomas in a xenograft mouse model . Cancer Lett   2016 ; 372 : 179 - 86 . 101. Bove   KE , McAdams   AJ . Composite ganglioneu...

... of virus . N Engl J Med   2006 ; 355 : 909 - 19 . 3. Glaze   E , Roy   M , Dalrymple   L , Lanning   L . A comparison of the pathogenesis of Marburg virus disease in humans and nonhuman primates and evaluation of the suitability of these animal models for predicting clinical efficacy...

... microorganisms primarily affect different cells: cardiomyocytes, endothelial cells, or inflammatory cells ( Table 7-2 ). As depicted in figure 7-1 , the pathogenesis of viral myocarditis is divided into three phases based on animal models and clinical observations ( 9 ). During the acute phase, there is direct...

...Table 6-1 DIFFERENCES BETWEEN HUMAN HERPESVIRUSES 1, 2, AND 3 HSV1 and 2 VZV Genome size; G+C content ~152Kbp; -67%(Approximately 50% genetic homology between HSV1 and 2) ~125Kbp; -47% Host range Broad Restricted (animal models do not replicate human disease) Route...

...   Y . Creutzfeldt-Jakob disease . Neuropathology   2017 ; 37 : 174 - 88 . 10. Brandner   S , Jaunmuktane   Z . Prion disease: experimental models and reality . Acta Neuropathol   2017 ; 133 : 197 - 222 . 11. WHO manual for surveillance of human transmissible spongiform...

...   2017 ; 38 : 264 - 76 . 10. Koh   AY . Murine models of Candida gastrointestinal colonization and dissemination . Eukaryot Cell   2013 ; 12 : 1416 - 22 . 11. Slavik   T . Human immunodeficiency virus-related gastrointestinal pathology: a southern Africa perspective with review...

... . 15. Rebman   AW , Aucott   JN . Post-treatment Lyme disease as a model for persistent symptoms in Lyme disease . Front Med (Lausanne)   2020 ; 7 : 57 . 16. Duray   P , Chandler   F . Lyme disease . In: Connor   D , Chandler   F , Schwartz   D , Manz   H , Lack...

... , Ehrhardt   D . Progress toward poliomyelitis eradication—Afghanistan, January 2018-May 2019 . MMWR Morb Mortal Wkly Rep   2019 ; 68 : 729 - 33 . 34. Shen   L , Chen   CY , Huang   D , et al . Pathogenic events in a nonhuman primate model of oral poliovirus infection leading...

... precludes exclusion of a mycelial phase at room temperature. In animal models, intradermal injection of the fungus obtained from human lesions results in localized multiplication of the yeasts. The organism elicits TGF-β (transforming growth factor-β), which suppresses macrophage lytic activity...

... Infect   2002 ; 4 : 1125 - 32 . 29. Savarino   SJ , Fasano   A , Robertson   DC , Levine   MM . Enteroaggregative Escherichia coli elaborate a heat-stable enterotoxin demonstrable in an in vitro rabbit intestinal model . J Clin Invest   1991 ; 87 : 1450 - 5 . 30. Darfeuille...

... changes. Pathologic features that have been observed in sepsis animal models, as well as patients who died from culture-proven sepsis include interstitial hemorrhages, thrombosis, edema, cellular apoptosis (including lymphocytes and hepatocytes), and foci of necrosis (presumably due to hypoperfusion...