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M Gallant

Showing results (211-220 of 236) with videos related to

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Journal of the American Veterinary Medical Association|September 24, 2005
Inheritance of recurrent exertional rhabdomyolysis in thoroughbredsPatricia K Dranchak, Stephanie J Valberg, Gary W Onan, et al.
Hospital Pediatrics|February 2, 2025
Implementing the Eat, Sleep, Console Model of Care: A Scoping ReviewSarah M Gallant, Kelly DeCoste, NaDeana Norris, et al.
Journal of Pediatric Hematology/Oncology|February 22, 2019
Hyperammonemia From Ureaplasma Infection in an Immunocompromised ChildNicholas Placone, Roy L Kao, Pamela Kempert, et al.
Nature Structural Biology|July 1, 1996
The three-dimensional structure of apopain/CPP32, a key mediator of apoptosisJ Rotonda, D W Nicholson, K M Fazil, et al.
Molecular Pharmacology|June 16, 2001
Prostaglandin receptor EP(4) mediates the bone anabolic effects of PGE(2)M Machwate, S Harada, C T Leu, et al.
American Journal of Medical Genetics. Part A|March 16, 2017
De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomaliesSureni V Mullegama, Steven D Klein, Milene V Mulatinho, et al.
Nature Communications|April 30, 2026
Amorphous intermediates and discovery of a kinetic polymorph of BiVO<sub>4</sub> from heating V+Bi+Zn single-source precursorsAlexandria E Hands, Thomas J Barnes, Andrea Scarperi, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Nature Genetics|November 28, 2006
Wnt-beta-catenin signaling initiates taste papilla developmentFei Liu, Shoba Thirumangalathu, Natalie M Gallant, et al.
Molecular Genetics and Metabolism|July 17, 2017
Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in CaliforniaN M Gallant, K Leydiker, Y Wilnai, et al.
Pageof 24

Showing results (211-220 of 236) with videos related to

Sort By:
Pageof 24
Journal of the American Veterinary Medical Association|September 24, 2005
Inheritance of recurrent exertional rhabdomyolysis in thoroughbredsPatricia K Dranchak, Stephanie J Valberg, Gary W Onan, et al.
Hospital Pediatrics|February 2, 2025
Implementing the Eat, Sleep, Console Model of Care: A Scoping ReviewSarah M Gallant, Kelly DeCoste, NaDeana Norris, et al.
Journal of Pediatric Hematology/Oncology|February 22, 2019
Hyperammonemia From Ureaplasma Infection in an Immunocompromised ChildNicholas Placone, Roy L Kao, Pamela Kempert, et al.
Nature Structural Biology|July 1, 1996
The three-dimensional structure of apopain/CPP32, a key mediator of apoptosisJ Rotonda, D W Nicholson, K M Fazil, et al.
Molecular Pharmacology|June 16, 2001
Prostaglandin receptor EP(4) mediates the bone anabolic effects of PGE(2)M Machwate, S Harada, C T Leu, et al.
American Journal of Medical Genetics. Part A|March 16, 2017
De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomaliesSureni V Mullegama, Steven D Klein, Milene V Mulatinho, et al.
Nature Communications|April 30, 2026
Amorphous intermediates and discovery of a kinetic polymorph of BiVO<sub>4</sub> from heating V+Bi+Zn single-source precursorsAlexandria E Hands, Thomas J Barnes, Andrea Scarperi, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Nature Genetics|November 28, 2006
Wnt-beta-catenin signaling initiates taste papilla developmentFei Liu, Shoba Thirumangalathu, Natalie M Gallant, et al.
Molecular Genetics and Metabolism|July 17, 2017
Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in CaliforniaN M Gallant, K Leydiker, Y Wilnai, et al.
Pageof 24