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C C Trenor

Showing results (1-10 of 7) with videos related to

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Genes & Development|March 29, 2001
A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) miceM D Fleming, D R Campagna, J N Haslett, et al.
Blood|July 27, 2000
The molecular defect in hypotransferrinemic miceC C Trenor, D R Campagna, V M Sellers, et al.
Blood|September 10, 1998
The G185R mutation disrupts function of the iron transporter Nramp2M A Su, C C Trenor, J C Fleming, et al.
Nature Genetics|August 1, 1997
Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter geneM D Fleming, C C Trenor, M A Su, et al.
Journal of Thrombosis and Haemostasis : JTH|October 6, 2017
Elevated preoperative von Willebrand factor is associated with perioperative thrombosis in infants and neonates with congenital heart diseaseR Hunt, C M Hoffman, S Emani, et al.
The Journal of Clinical Investigation|August 24, 2001
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) geneG Montosi, A Donovan, A Totaro, et al.
AJNR. American Journal of Neuroradiology|July 15, 2017
Transient Focal Neurologic Symptoms Correspond to Regional Cerebral Hypoperfusion by MRI: A Stroke Mimic in ChildrenL L Lehman, A R Danehy, C C Trenor, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Genes & Development|March 29, 2001
A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) miceM D Fleming, D R Campagna, J N Haslett, et al.
Blood|July 27, 2000
The molecular defect in hypotransferrinemic miceC C Trenor, D R Campagna, V M Sellers, et al.
Blood|September 10, 1998
The G185R mutation disrupts function of the iron transporter Nramp2M A Su, C C Trenor, J C Fleming, et al.
Nature Genetics|August 1, 1997
Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter geneM D Fleming, C C Trenor, M A Su, et al.
Journal of Thrombosis and Haemostasis : JTH|October 6, 2017
Elevated preoperative von Willebrand factor is associated with perioperative thrombosis in infants and neonates with congenital heart diseaseR Hunt, C M Hoffman, S Emani, et al.
The Journal of Clinical Investigation|August 24, 2001
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) geneG Montosi, A Donovan, A Totaro, et al.
AJNR. American Journal of Neuroradiology|July 15, 2017
Transient Focal Neurologic Symptoms Correspond to Regional Cerebral Hypoperfusion by MRI: A Stroke Mimic in ChildrenL L Lehman, A R Danehy, C C Trenor, et al.
Pageof 1