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Elena Torban

Showing results (31-40 of 37) with videos related to

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Plos One|May 17, 2019
Intrinsic tumor necrosis factor-α pathway is activated in a subset of patients with focal segmental glomerulosclerosisChen-Fang Chung, Thomas Kitzler, Nadezda Kachurina, et al.
Plos One|March 24, 2020
Differential role of planar cell polarity gene Vangl2 in embryonic and adult mammalian kidneysIda Derish, Jeremy K H Lee, Melanie Wong-King-Cheong, et al.
European Journal of Human Genetics : EJHG|November 1, 2021
Identification of a novel variant of the ciliopathic gene FUZZY associated with craniosynostosisWilliam B Barrell, Hadeel Adel Al-Lami, Jacqueline A C Goos, et al.
The New England Journal of Medicine|April 6, 2007
Mutations in VANGL1 associated with neural-tube defectsZoha Kibar, Elena Torban, Jonathan R McDearmid, et al.
Human Molecular Genetics|December 18, 2024
Use of patient-derived cell models for characterization of compound heterozygous hypomorphic C2CD3 variants in a patient with isolated nephronophthisisZachary T Sentell, Lina Mougharbel, Zachary W Nurcombe, et al.
Canadian Journal of Kidney Health and Disease|December 22, 2022
Advancing Discovery Research in Nephrology in Canada: A Conference Report From the 2021 Molecules and Mechanisms Mediating Kidney Health and Disease (M3K) Scientific Meeting and Investigator SummitDylan Burger, Amira Abdelrasoul, R Todd Alexander, et al.
Canadian Journal of Kidney Health and Disease|May 6, 2022
Can Peer Review Be Kinder? Supportive Peer Review: A Re-Commitment to Kindness and a Call to ActionCatherine M Clase, Elizabeth Dicks, Rachel Holden, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Plos One|May 17, 2019
Intrinsic tumor necrosis factor-α pathway is activated in a subset of patients with focal segmental glomerulosclerosisChen-Fang Chung, Thomas Kitzler, Nadezda Kachurina, et al.
Plos One|March 24, 2020
Differential role of planar cell polarity gene Vangl2 in embryonic and adult mammalian kidneysIda Derish, Jeremy K H Lee, Melanie Wong-King-Cheong, et al.
European Journal of Human Genetics : EJHG|November 1, 2021
Identification of a novel variant of the ciliopathic gene FUZZY associated with craniosynostosisWilliam B Barrell, Hadeel Adel Al-Lami, Jacqueline A C Goos, et al.
The New England Journal of Medicine|April 6, 2007
Mutations in VANGL1 associated with neural-tube defectsZoha Kibar, Elena Torban, Jonathan R McDearmid, et al.
Human Molecular Genetics|December 18, 2024
Use of patient-derived cell models for characterization of compound heterozygous hypomorphic C2CD3 variants in a patient with isolated nephronophthisisZachary T Sentell, Lina Mougharbel, Zachary W Nurcombe, et al.
Canadian Journal of Kidney Health and Disease|December 22, 2022
Advancing Discovery Research in Nephrology in Canada: A Conference Report From the 2021 Molecules and Mechanisms Mediating Kidney Health and Disease (M3K) Scientific Meeting and Investigator SummitDylan Burger, Amira Abdelrasoul, R Todd Alexander, et al.
Canadian Journal of Kidney Health and Disease|May 6, 2022
Can Peer Review Be Kinder? Supportive Peer Review: A Re-Commitment to Kindness and a Call to ActionCatherine M Clase, Elizabeth Dicks, Rachel Holden, et al.
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