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A C Reed

Showing results (31-40 of 39) with videos related to

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American Journal of Physiology. Renal Physiology|November 27, 2009
CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's diseaseAnita A C Reed, Nellie Y Loh, Sara Terryn, et al.
Oncogene|March 14, 2017
Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndromeG V Walls, M Stevenson, K E Lines, et al.
Nephron. Physiology|April 25, 2009
OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variabilityAntony E Shrimpton, Richard R Hoopes, Stephen J Knohl, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
Haematologica|May 30, 2024
The glutamate/aspartate transporter EAAT1 is crucial for T-cell acute lymphoblastic leukemia proliferation and survivalVesna S Stanulović, Shorog Al Omair, Michelle A C Reed, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Elife|September 2, 2022
Crosstalk between AML and stromal cells triggers acetate secretion through the metabolic rewiring of stromal cellsNuria Vilaplana-Lopera, Vincent Cuminetti, Ruba Almaghrabi, et al.
Nephron. Physiology|June 24, 2009
Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's diseaseFiona Wu, Anita A C Reed, Sian E Williams, et al.
Gigascience|December 12, 2018
PhenoMeNal: processing and analysis of metabolomics data in the cloudKristian Peters, James Bradbury, Sven Bergmann, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
American Journal of Physiology. Renal Physiology|November 27, 2009
CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's diseaseAnita A C Reed, Nellie Y Loh, Sara Terryn, et al.
Oncogene|March 14, 2017
Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndromeG V Walls, M Stevenson, K E Lines, et al.
Nephron. Physiology|April 25, 2009
OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variabilityAntony E Shrimpton, Richard R Hoopes, Stephen J Knohl, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
Haematologica|May 30, 2024
The glutamate/aspartate transporter EAAT1 is crucial for T-cell acute lymphoblastic leukemia proliferation and survivalVesna S Stanulović, Shorog Al Omair, Michelle A C Reed, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Elife|September 2, 2022
Crosstalk between AML and stromal cells triggers acetate secretion through the metabolic rewiring of stromal cellsNuria Vilaplana-Lopera, Vincent Cuminetti, Ruba Almaghrabi, et al.
Nephron. Physiology|June 24, 2009
Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's diseaseFiona Wu, Anita A C Reed, Sian E Williams, et al.
Gigascience|December 12, 2018
PhenoMeNal: processing and analysis of metabolomics data in the cloudKristian Peters, James Bradbury, Sven Bergmann, et al.
Pageof 4