PEX12 (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "PEX12" in Spanish language version.

Last modified: 05:32:42, 20 December 2025 (UTC)

Ref.Un. Ref.Website

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109nih.gov

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66doi.org

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55archive.org

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11wikidata.org

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11genecards.org

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11uniprot.org

2,402^nd place

2,752^nd place

archive.org (Global: 6^th place; Spanish: 4^th place)

«PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p». Mol. Cell. Biol. 18 (7): 4324-36. July 1998. PMC 109016. PMID 9632816. doi:10.1128/MCB.18.7.4324.
«PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import». J. Cell Biol. 147 (4): 761-74. November 1999. PMC 2156163. PMID 10562279. doi:10.1083/jcb.147.4.761.
«Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p». J. Biol. Chem. 275 (33): 25700-10. August 2000. PMID 10837480. doi:10.1074/jbc.M003303200.
«PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis». J. Cell Biol. 148 (5): 931-44. March 2000. PMC 2174547. PMID 10704444. doi:10.1083/jcb.148.5.931.
«Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences». Mol. Cell. Biol. 21 (13): 4413-24. July 2001. PMC 87101. PMID 11390669. doi:10.1128/MCB.21.13.4413-4424.2001.

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

dx.doi.org

«Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders». Nat Genet 15 (4): 385-8. April 1997. PMID 9090384. doi:10.1038/ng0497-385.
«PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p». Mol. Cell. Biol. 18 (7): 4324-36. July 1998. PMC 109016. PMID 9632816. doi:10.1128/MCB.18.7.4324.
«PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import». J. Cell Biol. 147 (4): 761-74. November 1999. PMC 2156163. PMID 10562279. doi:10.1083/jcb.147.4.761.
«Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p». J. Biol. Chem. 275 (33): 25700-10. August 2000. PMID 10837480. doi:10.1074/jbc.M003303200.
«PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis». J. Cell Biol. 148 (5): 931-44. March 2000. PMC 2174547. PMID 10704444. doi:10.1083/jcb.148.5.931.
«Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences». Mol. Cell. Biol. 21 (13): 4413-24. July 2001. PMC 87101. PMID 11390669. doi:10.1128/MCB.21.13.4413-4424.2001.

genecards.org (Global: low place; Spanish: 8,545^th place)

«PEX12 Gene - GeneCards | PEX12 Protein | PEX12 Antibody». www.genecards.org. Consultado el 9 de diciembre de 2020.

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

ncbi.nlm.nih.gov

«Human PubMed Reference:».
«Mouse PubMed Reference:».
«Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders». Nat Genet 15 (4): 385-8. April 1997. PMID 9090384. doi:10.1038/ng0497-385.
«Entrez Gene: PEX12 peroxisomal biogenesis factor 12».
«PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p». Mol. Cell. Biol. 18 (7): 4324-36. July 1998. PMC 109016. PMID 9632816. doi:10.1128/MCB.18.7.4324.
«PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import». J. Cell Biol. 147 (4): 761-74. November 1999. PMC 2156163. PMID 10562279. doi:10.1083/jcb.147.4.761.
«Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p». J. Biol. Chem. 275 (33): 25700-10. August 2000. PMID 10837480. doi:10.1074/jbc.M003303200.
«PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis». J. Cell Biol. 148 (5): 931-44. March 2000. PMC 2174547. PMID 10704444. doi:10.1083/jcb.148.5.931.
«Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences». Mol. Cell. Biol. 21 (13): 4413-24. July 2001. PMC 87101. PMID 11390669. doi:10.1128/MCB.21.13.4413-4424.2001.

uniprot.org (Global: 2,402^nd place; Spanish: 2,752^nd place)

«PEX12 - Peroxisome assembly protein 12 - Homo sapiens (Human) - PEX12 gene & protein». www.uniprot.org (en inglés). Consultado el 9 de diciembre de 2020.

wikidata.org (Global: 10^th place; Spanish: 253^rd place)

«Diseases that are genetically associated with PEX12 view/edit references on wikidata».

PEX12 (Spanish Wikipedia)

archive.org (Global: 6th place; Spanish: 4th place)

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

dx.doi.org

genecards.org (Global: low place; Spanish: 8,545th place)

nih.gov (Global: 5th place; Spanish: 5th place)