Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Clemens Bergwitz

Showing results (11-20 of 48) with videos related to

Pageof 5
Sort By:
Nature Reviews. Endocrinology|September 16, 2018
Role of phosphate sensing in bone and mineral metabolismSampada Chande, Clemens Bergwitz
Advances in Chronic Kidney Disease|March 17, 2011
Phosphate sensingClemens Bergwitz, Harald Jüppner
Journal of Molecular Endocrinology|December 18, 2020
FGF23 signalling and physiologyBryan B Ho, Clemens Bergwitz
Pflugers Archiv : European Journal of Physiology|August 16, 2018
Hereditary hypophosphatemic rickets with hypercalciuria: pathophysiology, clinical presentation, diagnosis and therapyClemens Bergwitz, Ken-Ichi Miyamoto
Therapeutic Advances in Musculoskeletal Disease|September 23, 2020
Description of a novel <i>SLC34A3.c.671delT</i> mutation causing hereditary hypophosphatemic rickets with hypercalciuria in two adolescent boys and response to recombinant human growth hormoneDaina Dreimane, Alyssa Chen, Clemens Bergwitz
Plos One|October 16, 2019
Transgenic mouse model for conditional expression of influenza hemagglutinin-tagged human SLC20A1/PIT1Sampada Chande, Bryan Ho, Jonathan Fetene, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutationPriya Phulwani, Clemens Bergwitz, Graciana Jaureguiberry, et al.
American Journal of Physiology. Renal Physiology|October 28, 2016
Impaired urinary osteopontin excretion in Npt2a-/- miceDaniel Caballero, Yuwen Li, Julian Ponsetto, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 11, 2008
A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3Kathleen Page, Clemens Bergwitz, Graciana Jaureguiberry, et al.
American Journal of Physiology. Renal Physiology|May 16, 2008
A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIcGraciana Jaureguiberry, Thomas O Carpenter, Stuart Forman, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Nature Reviews. Endocrinology|September 16, 2018
Role of phosphate sensing in bone and mineral metabolismSampada Chande, Clemens Bergwitz
Advances in Chronic Kidney Disease|March 17, 2011
Phosphate sensingClemens Bergwitz, Harald Jüppner
Journal of Molecular Endocrinology|December 18, 2020
FGF23 signalling and physiologyBryan B Ho, Clemens Bergwitz
Pflugers Archiv : European Journal of Physiology|August 16, 2018
Hereditary hypophosphatemic rickets with hypercalciuria: pathophysiology, clinical presentation, diagnosis and therapyClemens Bergwitz, Ken-Ichi Miyamoto
Therapeutic Advances in Musculoskeletal Disease|September 23, 2020
Description of a novel <i>SLC34A3.c.671delT</i> mutation causing hereditary hypophosphatemic rickets with hypercalciuria in two adolescent boys and response to recombinant human growth hormoneDaina Dreimane, Alyssa Chen, Clemens Bergwitz
Plos One|October 16, 2019
Transgenic mouse model for conditional expression of influenza hemagglutinin-tagged human SLC20A1/PIT1Sampada Chande, Bryan Ho, Jonathan Fetene, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutationPriya Phulwani, Clemens Bergwitz, Graciana Jaureguiberry, et al.
American Journal of Physiology. Renal Physiology|October 28, 2016
Impaired urinary osteopontin excretion in Npt2a-/- miceDaniel Caballero, Yuwen Li, Julian Ponsetto, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 11, 2008
A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3Kathleen Page, Clemens Bergwitz, Graciana Jaureguiberry, et al.
American Journal of Physiology. Renal Physiology|May 16, 2008
A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIcGraciana Jaureguiberry, Thomas O Carpenter, Stuart Forman, et al.
Pageof 5