Search Results - "Yang, Meiheng"

Expression of and Role for Ovarian Cancer G-protein-coupled Receptor 1 (OGR1) during Osteoclastogenesis by Yang, Meiheng, Mailhot, Geneviève, Birnbaum, Mark J., MacKay, Carole A., Mason-Savas, April, Odgren, Paul R.

“…Osteoclasts differentiate from hematopoietic mononuclear precursor cells under the control of both colony stimulating factor-1 (CSF-1, or M-CSF) and receptor…”
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Chemokine and chemokine receptor expression during colony stimulating factor-1–induced osteoclast differentiation in the toothless osteopetrotic rat: a key role for CCL9 (MIP-1γ) in osteoclastogenesis in vivo and in vitro by Yang, Meiheng, Mailhot, Geneviève, MacKay, Carole A., Mason-Savas, April, Aubin, Justin, Odgren, Paul R.

“…Osteoclasts differentiate from hematopoietic precursors under systemic and local controls. Chemokines and receptors direct leukocyte traffic throughout the…”
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BMP-5 expression increases during chondrocyte differentiation in vivo and in vitro and promotes proliferation and cartilage matrix synthesis in primary chondrocyte cultures by Mailhot, Geneviève, Yang, Meiheng, Mason-Savas, April, MacKay, Carole A., Leav, Irwin, Odgren, Paul R.

“…Bone morphogenetic proteins (BMPs) play pivotal roles in bone and cartilage growth and repair. Through phenotypes of short‐ear (se) mice, which have BMP‐5…”
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Septoclast Deficiency Accompanies Postnatal Growth Plate Chondrodysplasia in the Toothless ( tl ) Osteopetrotic, Colony-Stimulating Factor-1 (CSF-1)-Deficient Rat and Is Partially Responsive to CSF-1 Injections by Gartland, Alison, Mason-Savas, April, Yang, Meiheng, MacKay, Carole A, Birnbaum, Mark J, Odgren, Paul R

“…The septoclast is a specialized, cathepsin B-rich, perivascular cell type that accompanies invading capillaries on the metaphyseal side of the growth plate…”
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Differential expression and androgen regulation of the human selenium-binding protein gene hSP56 in prostate cancer cells by MEIHENG YANG, SYTKOWSKI, A. J

“…Low levels of dietary selenium are associated with increased risk of malignancy of several organs, including the prostate. Using a subtractive approach called…”
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False-Positive β-Galactosidase Staining in Osteoclasts by Endogenous Enzyme: Studies in Neonatal and Month-Old Wild-Type Mice by Odgren, Paul R., MacKay, Carole A., Mason-Savas, April, Yang, Meiheng, Mailhot, Geneviève, Birnbaum, Mark J.

“…Escherichia coli β-galactosidase (β-gal), encoded by the lacZ gene, has become an essential tool in studies of gene expression and function in higher…”
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Identification of genes expressed differentially by LNCaP or PC-3 prostate cancer cell lines by MEIHENG YANG, LODA, M, SYTKOWSKI, A. J

“…The transition from androgen-dependent to aggressive androgen-independent growth is an important development in prostate cancer, and the identification of…”
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Osteoclast stimulatory transmembrane protein (OC-STAMP), a novel protein induced by RANKL that promotes osteoclast differentiation by Yang, Meiheng, Birnbaum, Mark J., MacKay, Carole A., Mason-Savas, April, Thompson, Benjamin, Odgren, Paul R.

“…Microarray and real‐time RT‐PCR were used to examine expression changes in primary bone marrow cells and RAW 264.7 cells in response to RANKL. In silico…”
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A Gln-281 to Arg substitution in α-L-fucosidase is responsible for a common polymorphism detected by isoelectric focusing by MEIHENG YANG, DICIOCCO, R. A

“…A common polymorphism of human alpha-L-fucosidase consists of three phenotypes (Fu 1, Fu 2, and Fu 2-1) assigned by isoelectric focusing. The phenotypes are…”
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Using osteoclast differentiation as a model for gene discovery in an undergraduate cell biology laboratory by Birnbaum, Mark J., Picco, Jenna, Clements, Meghan, Witwicka, Hanna, Yang, Meiheng, Hoey, Margaret T., Odgren, Paul R.

“…A key goal of molecular/cell biology/biotechnology is to identify essential genes in virtually every physiological process to uncover basic mechanisms of cell…”
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Molecular cloning and characterization of rat CCL9 (MIP-1γ), the ortholog of mouse CCL9 by Yang, Meiheng, Odgren, Paul R.

“…We identified an EST sequence that was up-regulated during osteoclast formation in the rat. Investigating further, we cloned the cDNA from rat long bone and…”
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Polycationic Nanoparticles: (1) Synthesis of a Polylysine-MION Conjugate and its Application in Labeling Fibroblasts by Groman, Ernest V., Yang, Meiheng, Reinhardt, Christopher P., Weinberg, James S., Vaccaro, Dennis E.

“…Nanoparticles are increasingly used to label cells to track them by imaging or to quantify them in vivo. However, normal cellular uptake mechanisms are…”
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Cell Tracking Using Nanoparticles by Vaccaro, Dennis E., Yang, Meiheng, Weinberg, James S., Reinhardt, Christopher P., Groman, Ernest V.

“…Tracking cells in regenerative medicine is becoming increasingly important for basic cell therapy science, for cell delivery optimization and for accurate…”
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A Gln-281 to Arg substitution in ?-l-fucosidase is responsible for a common polymorphism detected by isoelectric focusing by Yang, Meiheng, DiCioccio, RichardA

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Cloning Differentially Expressed Genes by Linker Capture Subtraction by Yang, Meiheng, Sytkowski, Arthur J.

“…We have developed a simple and effective method, designated linker capture subtraction (LCS), for cloning differentially expressed genes between two cell types…”
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A mutation generating a stop codon in the alpha-L-fucosidase gene of a fucosidosis patient by Yang, M, Allen, H, DiCioccio, R A

“…Fucosidosis is an autosomal recessive, lysosomal storage disease featured by deficient activity of alpha-L-fucosidase. Lymphoid cell lines from a fucosidosis…”
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Pedigree analysis of alpha-L-fucosidase gene mutations in a fucosidosis family by Yang, M, Allen, H, DiCioccio, R A

“…Fucosidosis is an autosomal recessive lysosomal storage disease resulting from absence of alpha-L-fucosidase activity. Lymphoid cell lines from two siblings…”
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A missense mutation (G197?A) in the?-l-fucosidase gene of fucosidosis patients leads to loss of?-l-fucosidase by Yang, Meiheng, Allen, Howard, Fukushima, Hisao, DiCioccio, Richard A.

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A 66-Basepair insertion in Exon 6 of the α-L-fucosidase gene of a fucosidosis patient by Seo, Hee Chan, Yang, Meiheng, Kim, Alex H., O'Brien, John S., Dicioccio, Richard A., Gordon, Bruce A.

“…Fucosidosis is an autosomal recessive lysosomal storage disorder characterized by negligible activity of alpha -L-fucosidase. Fourteen different mutations…”
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A missense mutation (S63L) in alpha-L-fucosidase is responsible for fucosidosis in an Italian patient by Seo, H C, Yang, M, Tonlorenzi, R, Willems, P J, Kim, A H, Filocamo, M, Gatti, R, DiCioccio, R A, O'Brien, J S

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