Dietary phosphate modifies lifespan in Drosophila von BERGWITZ, Clemens

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Novel NaPi-IIc mutations causing HHRH and idiopathic hypercalciuria in several unrelated families: Long-term follow-up in one kindred von Yu, Y, Sanderson, S.R, Reyes, M, Sharma, A, Dunbar, N, Srivastava, T, Jüppner, H, Bergwitz, C

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Corrigendum to “Novel NaPi-IIc mutations causing HHRH and idiopathic hypercalciuria in several unrelated families: Long-term follow-up in one kindred” [Bone 50 (2012) 1100–1106]... von Yu, Y, Sanderson, S.R, Reyes, M, Sharma, A, Dunbar, N, Srivastava, T, Jüppner, H, Bergwitz, C

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Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis von Dasgupta, Debayan, Wee, Mark J, Reyes, Monica, Li, Yuwen, Simm, Peter J, Sharma, Amita, Schlingmann, Karl-Peter, Janner, Marco, Biggin, Andrew, Lazier, Joanna, Gessner, Michaela, Chrysis, Dionisios, Tuchman, Shamir, Baluarte, H Jorge, Levine, Michael A, Tiosano, Dov, Insogna, Karl, Hanley, David A, Carpenter, Thomas O, Ichikawa, Shoji, Hoppe, Bernd, Konrad, Martin, Sävendahl, Lars, Munns, Craig F, Lee, Hang, Jüppner, Harald, Bergwitz, Clemens

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SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phospha... von Bergwitz, Clemens, Roslin, Nicole M, Tieder, Martin, Loredo-Osti, J C, Bastepe, Murat, Abu-Zahra, Hilal, Frappier, Danielle, Burkett, Kelly, Carpenter, Thomas O, Anderson, Donald, Garabedian, Michele, Sermet, Isabelle, Fujiwara, T Mary, Morgan, Kenneth, Tenenhouse, Harriet S, Juppner, Harald

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Cellular Mechanism of Decreased Bone in Brtl Mouse Model of OI: Imbalance of Decreased Osteoblast Function and Increased Osteoclasts and Their Precursors von Uveges, Thomas E, Collin‐Osdoby, Patricia, Cabral, Wayne A, Ledgard, Felicia, Goldberg, Leah, Bergwitz, Clemens, Forlino, Antonella, Osdoby, Philip, Gronowicz, Gloria A, Marini, Joan C

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Brittle IV Mouse Model for Osteogenesis Imperfecta IV Demonstrates Postpubertal Adaptations to Improve Whole Bone Strength von Kozloff, Kenneth M, Carden, Angela, Bergwitz, Clemens, Forlino, Antonella, Uveges, Thomas E, Morris, Michael D, Marini, Joan C, Goldstein, Steven A

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A patient with autoimmune hepatitis type I, Addison's disease, atrophic thyroiditis, atrophic gastritis, exocrine pancreatic insufficiency, and heterozygous α1-Antitrypsin deficien... von BERGWITZ, C, BRABANT, G, TRAUTWEIN, C, MANNS, M. P

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A patient with autoimmune hepatitis type I, Addison's disease, atrophic thyroiditis, atrophic gastritis, exocrine pancreatic insufficiency, and heterozygous alpha1-antitrypsin defi... von Bergwitz, C, Brabant, G, Trautwein, C, Manns, M P

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Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia von Bergwitz, C., Prochnau, A., Mayr, B., Kramer, F.‐J., Rittierodt, M., Berten, H.‐L., Hausamen, J.‐E., Brabant, G.

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The Cadherin-Catenin System: Implications for Growth and Differentiation of Endocrine Tissues von Potter, E.

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Familial isolated parathyroid adenoma in a consanguineous family von BERQWITZ, C, BREMER, B, SOUDAH, B, MAYR, B, BRABANT, G

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Wnts differentially regulate colony growth and differentiation of chondrogenic rat calvaria cells von Bergwitz, Clemens, Wendlandt, Thomas, Kispert, Andreas, Brabant, Georg

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A versatile chondrogenic rat calvaria cell line R-tTA-24 that permits tetracycline-regulated gene expression von Bergwitz, C, Wendlandt, T, Pötter, E, Glomb, I, Gras, K, von zur Mühlen, A, Brabant, G

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Full activation of chimeric receptors by hybrids between parathyroid hormone and calcitonin. Evidence for a common pattern of ligand-receptor interaction von Bergwitz, C, Gardella, T J, Flannery, M R, Potts, Jr, J T, Kronenberg, H M, Goldring, S R, Jüppner, H

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Residues in the Membrane-spanning and Extracellular Loop Regions of the Parathyroid Hormone (PTH)-2 Receptor Determine Signaling Selectivity for PTH and PTH-related Peptide von Bergwitz, Clemens, Jusseaume, Scott A., Luck, Michael D., Jüppner, Harald, Gardella, Thomas J.

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A G protein-coupled receptor from zebrafish is activated by human parathyroid hormone and not by human or teleost parathyroid hormone-related peptide. Implications for the evolutio... von Rubin, D A, Hellman, P, Zon, L I, Lobb, C J, Bergwitz, C, Jüppner, H

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Polymorphism in exon M7 of the PTHR gene von Schipani, E., Hustmyer, F.G., Bergwitz, C., Jūppner, H.

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A patient with autoimmune hepatitis type I, Addison's disease, atrophic thyroiditis, atrophic gastritis, exocrine pancreatic insufficiency, and heterozygous a sub(1)-antitrypsin de... von Bergwitz, C, Brabant, G, Trautwein, C, Manns, M P

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A Patient With Autoimmune Hepatitis Type I, Addison's Disease, Atrophic Thyroiditis, Atrophic Gastritis, Exocrine Pancreatic Insufficiency, and Heterozygous α1-Antitrypsin Deficien... von Bergwitz, C, Brabant, G, Trautwein, C, Manns, M P

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