Leillani L Ha
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Explore the profile of Leillani L Ha including associated specialties, affiliations and a list of published articles.
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5
Citations
17
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Recent Articles
1.
Alves C, Das S, Krishnan V, Ha L, Fox L, Stutzman H, et al.
bioRxiv
. 2024 Nov;
PMID: 39605323
Genetic vascular disorders are prevalent diseases that have diverse etiologies and few treatment options. Pathogenic missense mutations in the alpha actin isotype 2 gene () primarily affect smooth muscle cell...
2.
Fry M, Navarro P, Hakim P, Ananda V, Qin X, Landoni J, et al.
EMBO J
. 2024 Jan;
43(3):391-413.
PMID: 38225406
Cristae membrane state plays a central role in regulating mitochondrial function and cellular metabolism. The protein Optic atrophy 1 (Opa1) is an important crista remodeler that exists as two forms...
3.
Alves C, Ha L, Yaworski R, Sutton E, Lazzarotto C, Christie K, et al.
Nat Biomed Eng
. 2023 Dec;
8(2):118-131.
PMID: 38057426
Spinal muscular atrophy (SMA) is caused by mutations in SMN1. SMN2 is a paralogous gene with a C•G-to-T•A transition in exon 7, which causes this exon to be skipped in...
4.
Alves C, Ha L, Yaworski R, Lazzarotto C, Christie K, Reilly A, et al.
bioRxiv
. 2023 Jan;
PMID: 36711797
Spinal muscular atrophy (SMA) is a devastating neuromuscular disease caused by mutations in the gene. Despite the development of various therapies, outcomes can remain suboptimal in SMA infants and the...
5.
Fry M, Navarro P, Hakim P, Ananda V, Qin X, Landoni J, et al.
bioRxiv
. 2023 Jan;
PMID: 36711707
Cristae membrane state plays a central role in regulating mitochondrial function and cellular metabolism. The protein Optic atrophy 1 (Opa1) is an important crista remodeler that exists as two forms...