The Core Microscopy and Molecular Histology laboratory provides not only services in routine microscopic techniques such as tissue preparation and analysis by light and electron microscopy for contemporary analytical morphological methods, including immunohistochemistry, immuno-electron microscopy, isotopic and non-isotopic in situ hybridization and digital imaging technology (such as quantitative analysis of microscopic images, and generation of composite images and slides using computer imaging tools). The Microscopy and Molecular Histology Laboratory has also been involved in teaching and training a large number of undergraduate and graduate students, research associates, visiting fellows and residents, while working on different Program Project-related studies. The facility of Core B consists of two physically separate suites of laboratories, with a total of 1,400 square feet (600 square feet + 800 square feet), where separate modules are dedicated to experimental procedures and tissue collection, tissue fixation and processing (dehydration, embedding, resin polymerization, etc.), histology (frozen and paraffin sectioning), ultramicrotomy, cryoultramicrotomy, microscopy (light, fluorescence and electron microscopy), and darkroom work. The personnel of Core B are Laszlo G. Komuves, Ph.D., Director, Dr. Corey Largman, Co-director, and Ms. Angela Kwong, Technician. The Microscopy and Molecular Histology Laboratory has provided not only services (including preparation of fixatives, processing and embedding of tissue samples, and immunohistochemistry or in situ hybridization) for the investigators of the Program Project, but it also has been involved actively in the planning of experiments, and in the analysis and interpretation of the data. The Microscopy and Molecular Histology Laboratory is committed to improving transitional morphological methods; to introduce newly developed techniques; and to devise novel microscopic methods for studying the biology of keratinocytes and the skin. With this background in histologic, electron microscopic, immunohistochemical and in situ hybridization techniques, the Microscopy and Molecular Histology Laboratory will continue to advise and assist investigators of the Program Project with their microscopic and morphological studies, as required. A list of publications that have resulted from these interactions is appended (see List of Publications).

Project Start
1999-08-01
Project End
2000-07-31
Budget Start
Budget End
Support Year
11
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Northern California Institute Research & Education
Department
Type
DUNS #
City
San Francisco
State
CA
Country
United States
Zip Code
94121
Bikle, Daniel D (2016) Extraskeletal actions of vitamin D. Ann N Y Acad Sci 1376:29-52
Bikle, Daniel D; Oda, Yuko; Tu, Chia-Ling et al. (2015) Novel mechanisms for the vitamin D receptor (VDR) in the skin and in skin cancer. J Steroid Biochem Mol Biol 148:47-51
Bikle, Daniel D (2014) Vitamin D metabolism, mechanism of action, and clinical applications. Chem Biol 21:319-29
Bikle, Daniel D (2014) Vitamin D and cancer: the promise not yet fulfilled. Endocrine 46:29-38
Bikle, Daniel D (2014) The vitamin D receptor: a tumor suppressor in skin. Adv Exp Med Biol 810:282-302
Tu, Chia-Ling; Bikle, Daniel D (2013) Role of the calcium-sensing receptor in calcium regulation of epidermal differentiation and function. Best Pract Res Clin Endocrinol Metab 27:415-27
Jiang, Yan J; Kim, Peggy; Uchida, Yoshikazu et al. (2013) Ceramides stimulate caspase-14 expression in human keratinocytes. Exp Dermatol 22:113-8
Bikle, Daniel D (2012) Vitamin D and the skin: Physiology and pathophysiology. Rev Endocr Metab Disord 13:3-19
Bourguignon, L Y W; Earle, C; Wong, G et al. (2012) Stem cell marker (Nanog) and Stat-3 signaling promote MicroRNA-21 expression and chemoresistance in hyaluronan/CD44-activated head and neck squamous cell carcinoma cells. Oncogene 31:149-60
Tu, Chia-Ling; Crumrine, Debra A; Man, Mao-Qiang et al. (2012) Ablation of the calcium-sensing receptor in keratinocytes impairs epidermal differentiation and barrier function. J Invest Dermatol 132:2350-2359

Showing the most recent 10 out of 223 publications