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Clemens Bergwitz

Showing results (31-40 of 48) with videos related to

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Plos One|February 24, 2012
Roles of major facilitator superfamily transporters in phosphate response in DrosophilaClemens Bergwitz, Matthew D Rasmussen, Charles DeRobertis, et al.
Nutrition Research (New York, N.Y.)|January 15, 2021
Different elemental infant formulas show equivalent phosphorus and calcium bioavailability in healthy volunteersClemens Bergwitz, Simone R B M Eussen, Pilou L H R Janssens, et al.
Kidney International Reports|August 24, 2019
Description of 5 Novel <i>SLC34A3/</i>NPT2c Mutations Causing Hereditary Hypophosphatemic Rickets With HypercalciuriaAlyssa Chen, Hannah Ro, Venkat Ram Rakesh Mundra, et al.
The Journal of Biological Chemistry|November 5, 2010
Acute down-regulation of sodium-dependent phosphate transporter NPT2a involves predominantly the cAMP/PKA pathway as revealed by signaling-selective parathyroid hormone analogsSo Nagai, Makoto Okazaki, Hiroko Segawa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 10, 2004
Brittle IV mouse model for osteogenesis imperfecta IV demonstrates postpubertal adaptations to improve whole bone strengthKenneth M Kozloff, Angela Carden, Clemens Bergwitz, et al.
American Journal of Medical Genetics. Part A|May 23, 2023
Multifocal heterotopic ossification in a man with germline variants of LIM Mineralization Protein-1 (LMP-1)Sreedhara Sangadala, Eileen M Shore, Meiqi Xu, et al.
Cell Reports|June 27, 2024
Both enantiomers of β-aminoisobutyric acid BAIBA regulate Fgf23 via MRGPRD receptor by activating distinct signaling pathways in osteocytesEijiro Sakamoto, Yukiko Kitase, Alexander J Fitt, et al.
The Journal of Clinical Endocrinology and Metabolism|August 7, 2012
Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutationsMichael Mannstadt, Daniella Magen, Hiroko Segawa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 8, 2008
Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursorsThomas E Uveges, Patricia Collin-Osdoby, Wayne A Cabral, et al.
Calcified Tissue International|November 19, 2023
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic ReviewManjunath Havalappa Dodamani, Saba Samad Memon, Manjiri Karlekar, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Plos One|February 24, 2012
Roles of major facilitator superfamily transporters in phosphate response in DrosophilaClemens Bergwitz, Matthew D Rasmussen, Charles DeRobertis, et al.
Nutrition Research (New York, N.Y.)|January 15, 2021
Different elemental infant formulas show equivalent phosphorus and calcium bioavailability in healthy volunteersClemens Bergwitz, Simone R B M Eussen, Pilou L H R Janssens, et al.
Kidney International Reports|August 24, 2019
Description of 5 Novel <i>SLC34A3/</i>NPT2c Mutations Causing Hereditary Hypophosphatemic Rickets With HypercalciuriaAlyssa Chen, Hannah Ro, Venkat Ram Rakesh Mundra, et al.
The Journal of Biological Chemistry|November 5, 2010
Acute down-regulation of sodium-dependent phosphate transporter NPT2a involves predominantly the cAMP/PKA pathway as revealed by signaling-selective parathyroid hormone analogsSo Nagai, Makoto Okazaki, Hiroko Segawa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 10, 2004
Brittle IV mouse model for osteogenesis imperfecta IV demonstrates postpubertal adaptations to improve whole bone strengthKenneth M Kozloff, Angela Carden, Clemens Bergwitz, et al.
American Journal of Medical Genetics. Part A|May 23, 2023
Multifocal heterotopic ossification in a man with germline variants of LIM Mineralization Protein-1 (LMP-1)Sreedhara Sangadala, Eileen M Shore, Meiqi Xu, et al.
Cell Reports|June 27, 2024
Both enantiomers of β-aminoisobutyric acid BAIBA regulate Fgf23 via MRGPRD receptor by activating distinct signaling pathways in osteocytesEijiro Sakamoto, Yukiko Kitase, Alexander J Fitt, et al.
The Journal of Clinical Endocrinology and Metabolism|August 7, 2012
Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutationsMichael Mannstadt, Daniella Magen, Hiroko Segawa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 8, 2008
Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursorsThomas E Uveges, Patricia Collin-Osdoby, Wayne A Cabral, et al.
Calcified Tissue International|November 19, 2023
Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic ReviewManjunath Havalappa Dodamani, Saba Samad Memon, Manjiri Karlekar, et al.
Pageof 5