HADHB (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "HADHB" in English language version.

Last modified: 22:00:05, 29 September 2025 (UTC)

Ref.Un. Ref.Website

Global rank English rank

2118nih.gov

5^th place

1010doi.org

2^nd place

62ensembl.org

630^th place

326^th place

22semanticscholar.org

15^th place

8^th place

11web.archive.org

1^st place

11heartproteome.org

low place

doi.org (Global: 2^nd place; English: 2^nd place)

]Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–1053. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
Spiekerkoetter U, Khuchua Z, Yue Z, Bennett MJ, Strauss AW (February 2004). "General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover". Pediatric Research. 55 (2): 190–196. doi:10.1203/01.pdr.0000103931.80055.06. PMID 14630990.
Sonta SI, Sandberg AA (1977). "Chromosomes and causation of human cancer and leukemia: XXVIII. Value of detailed chromosome studies on large numbers of cells in CML". American Journal of Hematology. 3 (2): 121–126. doi:10.1002/ajh.2830030202. PMID 272120. S2CID 13141165.
Spiekerkoetter U, Sun B, Khuchua Z, Bennett MJ, Strauss AW (June 2003). "Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to beta-subunit mutations". Human Mutation. 21 (6): 598–607. doi:10.1002/humu.10211. PMID 12754706. S2CID 85671653.
den Boer ME, Dionisi-Vici C, Chakrapani A, van Thuijl AO, Wanders RJ, Wijburg FA (June 2003). "Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement". The Journal of Pediatrics. 142 (6): 684–689. doi:10.1067/mpd.2003.231. PMID 12838198.
Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, et al. (October 1992). "Combined enzyme defect of mitochondrial fatty acid oxidation". The Journal of Clinical Investigation. 90 (4): 1219–1225. doi:10.1172/jci115983. PMC 443162. PMID 1401059.
Hong YB, Lee JH, Park JM, Choi YR, Hyun YS, Yoon BR, et al. (December 2013). "A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease". BMC Medical Genetics. 14 125. doi:10.1186/1471-2350-14-125. PMC 4029087. PMID 24314034.
Zhou Z, Zhou J, Du Y (July 2012). "Estrogen receptor alpha interacts with mitochondrial protein HADHB and affects beta-oxidation activity". Molecular & Cellular Proteomics. 11 (7) M111.011056. doi:10.1074/mcp.m111.011056. PMC 3394935. PMID 22375075.
Adams DJ, Beveridge DJ, van der Weyden L, Mangs H, Leedman PJ, Morris BJ (November 2003). "HADHB, HuR, and CP1 bind to the distal 3'-untranslated region of human renin mRNA and differentially modulate renin expression". The Journal of Biological Chemistry. 278 (45): 44894–44903. doi:10.1074/jbc.m307782200. PMID 12933794.
Downie Ruiz Velasco A, Welten SM, Goossens EA, Quax PH, Rappsilber J, Michlewski G, et al. (March 2019). "Posttranscriptional Regulation of 14q32 MicroRNAs by the CIRBP and HADHB during Vascular Regeneration after Ischemia". Molecular Therapy. Nucleic Acids. 14: 329–338. doi:10.1016/j.omtn.2018.11.017. PMC 6350214. PMID 30665182.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000138029 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000059447 – Ensembl, May 2017

heartproteome.org (Global: low place; English: low place)

"Trifunctional enzyme subunit beta, mitochondrial". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 4 March 2016. Retrieved 23 March 2015.

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

]Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–1053. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
Spiekerkoetter U, Khuchua Z, Yue Z, Bennett MJ, Strauss AW (February 2004). "General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover". Pediatric Research. 55 (2): 190–196. doi:10.1203/01.pdr.0000103931.80055.06. PMID 14630990.
Sonta SI, Sandberg AA (1977). "Chromosomes and causation of human cancer and leukemia: XXVIII. Value of detailed chromosome studies on large numbers of cells in CML". American Journal of Hematology. 3 (2): 121–126. doi:10.1002/ajh.2830030202. PMID 272120. S2CID 13141165.
Spiekerkoetter U, Sun B, Khuchua Z, Bennett MJ, Strauss AW (June 2003). "Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to beta-subunit mutations". Human Mutation. 21 (6): 598–607. doi:10.1002/humu.10211. PMID 12754706. S2CID 85671653.
den Boer ME, Dionisi-Vici C, Chakrapani A, van Thuijl AO, Wanders RJ, Wijburg FA (June 2003). "Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement". The Journal of Pediatrics. 142 (6): 684–689. doi:10.1067/mpd.2003.231. PMID 12838198.
Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, et al. (October 1992). "Combined enzyme defect of mitochondrial fatty acid oxidation". The Journal of Clinical Investigation. 90 (4): 1219–1225. doi:10.1172/jci115983. PMC 443162. PMID 1401059.
Hong YB, Lee JH, Park JM, Choi YR, Hyun YS, Yoon BR, et al. (December 2013). "A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease". BMC Medical Genetics. 14 125. doi:10.1186/1471-2350-14-125. PMC 4029087. PMID 24314034.
Zhou Z, Zhou J, Du Y (July 2012). "Estrogen receptor alpha interacts with mitochondrial protein HADHB and affects beta-oxidation activity". Molecular & Cellular Proteomics. 11 (7) M111.011056. doi:10.1074/mcp.m111.011056. PMC 3394935. PMID 22375075.
Adams DJ, Beveridge DJ, van der Weyden L, Mangs H, Leedman PJ, Morris BJ (November 2003). "HADHB, HuR, and CP1 bind to the distal 3'-untranslated region of human renin mRNA and differentially modulate renin expression". The Journal of Biological Chemistry. 278 (45): 44894–44903. doi:10.1074/jbc.m307782200. PMID 12933794.
Downie Ruiz Velasco A, Welten SM, Goossens EA, Quax PH, Rappsilber J, Michlewski G, et al. (March 2019). "Posttranscriptional Regulation of 14q32 MicroRNAs by the CIRBP and HADHB during Vascular Regeneration after Ischemia". Molecular Therapy. Nucleic Acids. 14: 329–338. doi:10.1016/j.omtn.2018.11.017. PMC 6350214. PMID 30665182.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl-Coenzyme A hydratase (trifunctional protein)".
]Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, et al. (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–1053. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, et al. (October 1992). "Combined enzyme defect of mitochondrial fatty acid oxidation". The Journal of Clinical Investigation. 90 (4): 1219–1225. doi:10.1172/jci115983. PMC 443162. PMID 1401059.
Hong YB, Lee JH, Park JM, Choi YR, Hyun YS, Yoon BR, et al. (December 2013). "A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease". BMC Medical Genetics. 14 125. doi:10.1186/1471-2350-14-125. PMC 4029087. PMID 24314034.
Zhou Z, Zhou J, Du Y (July 2012). "Estrogen receptor alpha interacts with mitochondrial protein HADHB and affects beta-oxidation activity". Molecular & Cellular Proteomics. 11 (7) M111.011056. doi:10.1074/mcp.m111.011056. PMC 3394935. PMID 22375075.
Downie Ruiz Velasco A, Welten SM, Goossens EA, Quax PH, Rappsilber J, Michlewski G, et al. (March 2019). "Posttranscriptional Regulation of 14q32 MicroRNAs by the CIRBP and HADHB during Vascular Regeneration after Ischemia". Molecular Therapy. Nucleic Acids. 14: 329–338. doi:10.1016/j.omtn.2018.11.017. PMC 6350214. PMID 30665182.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

Sonta SI, Sandberg AA (1977). "Chromosomes and causation of human cancer and leukemia: XXVIII. Value of detailed chromosome studies on large numbers of cells in CML". American Journal of Hematology. 3 (2): 121–126. doi:10.1002/ajh.2830030202. PMID 272120. S2CID 13141165.
Spiekerkoetter U, Sun B, Khuchua Z, Bennett MJ, Strauss AW (June 2003). "Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to beta-subunit mutations". Human Mutation. 21 (6): 598–607. doi:10.1002/humu.10211. PMID 12754706. S2CID 85671653.

web.archive.org (Global: 1^st place; English: 1^st place)

"Trifunctional enzyme subunit beta, mitochondrial". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 4 March 2016. Retrieved 23 March 2015.

HADHB (English Wikipedia)

doi.org (Global: 2nd place; English: 2nd place)

ensembl.org (Global: 630th place; English: 326th place)