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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 2 |
1996 | 1 |
1998 | 1 |
2000 | 1 |
2015 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (cited) for id: 613898
7 results
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Page 1
Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers.
Mol Genet Metab. 2022 Nov;137(3):257-264. doi: 10.1016/j.ymgme.2022.09.008. Epub 2022 Sep 30.
Mol Genet Metab. 2022.
PMID: 36228350
Disturbance of redox homeostasis as a contributing underlying pathomechanism of brain and liver alterations in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
Leipnitz G, Vargas CR, Wajner M.
Leipnitz G, et al.
J Inherit Metab Dis. 2015 Nov;38(6):1021-8. doi: 10.1007/s10545-015-9863-3. Epub 2015 Jun 4.
J Inherit Metab Dis. 2015.
PMID: 26041581
Review.
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Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency.
Muroi J, Yorifuji T, Uematsu A, Shigematsu Y, Onigata K, Maruyama H, Nobutoki T, Kitamura A, Nakahata T.
Muroi J, et al.
Hum Genet. 2000 Oct;107(4):320-6. doi: 10.1007/s004390000363.
Hum Genet. 2000.
PMID: 11129331
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HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q.
Mitchell GA, Ozand PT, Robert MF, Ashmarina L, Roberts J, Gibson KM, Wanders RJ, Wang S, Chevalier I, Plöchl E, Miziorko H.
Mitchell GA, et al.
Am J Hum Genet. 1998 Feb;62(2):295-300. doi: 10.1086/301730.
Am J Hum Genet. 1998.
PMID: 9463337
Free PMC article.
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3-Hydroxy-3-methylglutaryl CoA lyase (HL): mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patients.
Wang SP, Robert MF, Gibson KM, Wanders RJ, Mitchell GA.
Wang SP, et al.
Genomics. 1996 Apr 1;33(1):99-104. doi: 10.1006/geno.1996.0164.
Genomics. 1996.
PMID: 8617516
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3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency.
Mitchell GA, Robert MF, Hruz PW, Wang S, Fontaine G, Behnke CE, Mende-Mueller LM, Schappert K, Lee C, Gibson KM, Miziorko HM, et al.
Mitchell GA, et al.
J Biol Chem. 1993 Feb 25;268(6):4376-81.
J Biol Chem. 1993.
PMID: 8440722
Free article.
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3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes.
Wang S, Nadeau JH, Duncan A, Robert MF, Fontaine G, Schappert K, Johnson KR, Zietkiewicz E, Hruz P, Miziorko H, et al.
Wang S, et al.
Mamm Genome. 1993;4(7):382-7. doi: 10.1007/BF00360589.
Mamm Genome. 1993.
PMID: 8102917
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