Search Results - Kedlaya, Rajendra
- Showing 1 - 9 results of 9
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Mutation in Archain 1, a Subunit of COPI Coatomer Complex, Causes Diluted Coat Color and Purkinje Cell Degeneration by Xu, Xinjie, Kedlaya, Rajendra, Higuchi, Hitoshi, Ikeda, Sakae, Justice, Monica J., Setaluri, Vijayasaradhi, Ikeda, Akihiro
Published 2010Text -
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Calcium homeostasis in human melanocytes: role of transient receptor potential melastatin 1 (TRPM1) and its regulation by ultraviolet light by Devi, Sulochana, Kedlaya, Rajendra, Maddodi, Nityanand, Bhat, Kumar M. R., Weber, Craig S., Valdivia, Hector, Setaluri, Vijayasaradhi
Published 2009Text -
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Anabolic and Catabolic Regimens of Human Parathyroid Hormone 1–34 Elicit Bone- and Envelope-Specific Attenuation of Skeletal Effects in Sost-Deficient Mice by Robling, Alexander G., Kedlaya, Rajendra, Ellis, Shana N., Childress, Paul J., Bidwell, Joseph P., Bellido, Teresita, Turner, Charles H.
Published 2011Text -
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High-bone-mass causing mutant LRP5 receptors are resistant to endogenous inhibitors in vivo() by Niziolek, Paul J., MacDonald, Bryan T., Kedlaya, Rajendra, Zhang, Minjie, Bellido, Teresita, He, Xi, Warman, Matthew L., Robling, Alexander G.
Published 2015Text -
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Adult-Onset Deletion of β-Catenin in (10kb)Dmp1-Expressing Cells Prevents Intermittent PTH-Induced Bone Gain by Kedlaya, Rajendra, Kang, Kyung Shin, Hong, Jung Min, Bettagere, Vidya, Lim, Kyung-Eun, Horan, Daniel, Divieti-Pajevic, Paola, Robling, Alexander G.
Published 2016Text -
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Sclerostin Inhibition Reverses Skeletal Fragility in an Lrp5-Deficient Mouse Model of OPPG Syndrome by Kedlaya, Rajendra, Veera, Shreya, Horan, Daniel J., Moss, Rachel E., Ayturk, Ugur M., Jacobsen, Christina M., Bowen, Margot E., Paszty, Chris, Warman, Matthew L., Robling, Alexander G.
Published 2013Text