(A) Vascular endothelial growth factor D (VEGF-D) staining in luminal ductal cells with occasional staining in myoepithelial cells of normal breast.  (A)

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(A) Programmed cell death ligand-1 (PD-L1) expression score was significantly higher in pulmonary adenocarcinomas with grade G2/G3 differentiation as compared.
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Characteristics of advanced fibrosis in usual interstitial pneumonia of idiopathic pulmonary fibrosis include a subpleural distribution of fibrosis (A,
Stratified mucinous intraepithelial lesion in which stratified epithelium resembling cervical intraepithelial neoplasia contains abundant mucin globules.
Persistence of first tumour necrosis factor alpha inhibitor (TNFi) by TNFi Kaplan-Meier plot of time (years) to discontinuation of treatment by TNFi. (A)
Catecholamines and metabolites expressed for each mole of creatinine in single voided urine specimens on one preoperative (day 0) and four postoperative.
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Demonstration of Helicobacter pylori by the four staining methods: (A) modified Giemsa, (B) anti-H pylori antibody immunostain, (C) modified McMullen's.
 (A,B) mRNA in situ hybridisation (ISH) with Epstein–Barr virus-encoded small RNA-1 probe in a case of Hodgkin’s lymphoma focally affecting the bone marrow.
(A) The two tumours at the end of the ascending and transverse colon are indicated by the arrows. (A) The two tumours at the end of the ascending and transverse.
 Pilomatricoma: (A) a multilobulated mass in fibrous stroma reaching the subcutis; (B) basaloid and ghost cells; (C) mitoses in an early lesion; and (D)
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Response of Calu-6 tumors to anti-VEGF therapy.
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A 47-year-old man with acute necrotising pancreatitis complicated by infected pancreatic necrosis. A 47-year-old man with acute necrotising pancreatitis.
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Immunolocalisation of MUC2 core antigen.
Histopathology of SGAT
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 (A) Vascular endothelial growth factor D (VEGF-D) staining in luminal ductal cells with occasional staining in myoepithelial cells of normal breast.  (A) Vascular endothelial growth factor D (VEGF-D) staining in luminal ductal cells with occasional staining in myoepithelial cells of normal breast. (B) Expression in areas of cystic disease, with enhanced VEGF-D expression in duct epithelial cells (inset: nerve and stromal cells that are also immunopositive). (C) Heterogeneous staining of VEGF-D in malignant epithelium in a poorly differentiated tumour and (D) a well differentiated tumour with granular staining at the apical pole of glands. (E) Enhanced VEGF-D immunostaining at the periphery of a tumour (arrows) without upregulation in an adjacent area of necrosis (asterisk). (F) Strong staining for VEGF-D in a lymphatic tumour embolus. M J Currie et al. J Clin Pathol 2004;57:829-834 Copyright © by the BMJ Publishing Group Ltd & Association of Clinical Pathologists. All rights reserved.