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  • Book
    Fan Lin, Jeffrey W. Prichard, Haiyan Liu, Myra L. Wilkerson, editors.
    Summary: As in the second edition, the third edition of Handbook of Practical Immunohistochemistry Frequently Asked Questions is written in a question and answer (Q & A) format and intended to be a practical, user-friendly, quick reference for information related to using the most up-to-date immunohistochemistry and in situ hybridization in clinical diagnosis. The new edition demonstrates a significant revision and improvement over the second edition. Five new chapters have been added that cover the following: 1) Immunohistochemistry: Leicas perspective; 2) Immunohistochemistry: Maixin perspective; 3) RNA in situ hybridization: Applications in anatomic pathology; 4) Applications of rapid immunohistochemistry on frozen tissue sections during intraoperative pathologic diagnosis; and 5) Cutaneous lymphomas. In addition to extensive additions and changes, over 150 new questions and answers were added throughout this new edition. All chapters have been updated to include relevant new questions, new markers, more refined IHC panels, representative pictures, and current references. An extensive set of high-quality color pictures and diagnostic algorithms, if available, is included in each chapter to illustrate some of the key antibodies, including many recently discovered and substantiated antibodies used in that chapter. Written by experts in the field, Handbook of Practical Immunohistochemistry Third Edition is a comprehensive and practical guide for surgical pathologists, pathology residents and fellows, cytopathologists, and cytotechnologists.

    Contents:
    1. Immunohistochemistry Quality Management And Regulation
    2. Standardization of Diagnostic Immunohistochemistry
    3. Automated Immunohistochemistry Overview
    4. Immunohistochemistry: An Agilent Perspective
    5. The Leica Biosystems Perspective : From excision to imaging every step is critical
    6. Immunohistochemistry: Maixin Perspective
    7. Immunohistochemistry: Roche Tissue Diagnostics Perspective
    8. Applications Of Rapid Immunohistochemistry On Frozen Tissue Sections During Intraoperative Pathological Diagnoses
    9. RNA In Situ Hybridization: Applications in Anatomic Pathology
    10. Overview of Immunohistochemistry Assessment of Cancer-Related Predictive Biomarkers and Common Genetic Alterations
    11. Tissue Microarray
    12. Unknown Primary/Undifferentiated Neoplasm
    13. Exfoliative Cytology And Effusions
    14. Breast
    15. Predictive Biomarkers In Breast Cancer: ER, PR And HER-2/NEU
    16. Central Nerve System
    17. Thyroid, Parathyroid, and Adrenal glands
    18. Salivary Glands and Head and Neck
    19. Pleuropulmonary And Mediastinal Neoplasms
    20. Uterus
    21. Ovary
    22. Prostate Gland
    23. Urinary Bladder And Urachus
    24. Kidney
    25. Testis And Paratesticular Tissues
    26. Pancreas And Ampulla
    27. Liver, Bile Ducts And GallBladder
    28. Upper Gastrointestinal Tract
    29. Lower Gastrointestinal Tract And Microsatellite Instability (MSI)
    30. Soft Tissue and Bone Tumors
    31. Lymph Node
    32. Bone Marrow
    33. Cutaneous Lymphomas
    34. Infectious diseases
    35. Skin
    36. Application of Direct Immunofluorescence for Skin and Mucosal Biopsies: A Practical Review
    37. Application Of Fluorescent In Situ Hybridization (FISH) In Surgical And Cytologic Specimens (Solid Tumors, Hematopoietic Tumors, Urine, Bile Duct Brushing And Bronchoscopy).
    Digital Access Springer 2022
  • Article
    Horii D, Kanayama T, Mori M, Shibasaki M, Ikegami S.
    Eur J Pharmacol. 1978 Oct 01;51(3):313-6.
    The action of 9(0)-thiaprostacyclin (PGI2-S) was compared with that of prostacyclin (PGI2) and papaverine in the femoral circulation of dogs. PGI2-S, injected into the dog femoral artery in a dose of 0.1 microgram or higher, produced marked vasodilation in the femoral artery without any change in blood pressure. The potentcy of PGI2-S was one tenth that of PGI2, and was a hundred times that of papaverine. The stability of PGI2-S in neutral solution was forty times that of PGI2.
    Digital Access Access Options