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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease.
Mol Neurodegener. 2011 May 19;6(1):32. doi: 10.1186/1750-1326-6-32.
Mol Neurodegener. 2011.
PMID: 21595933
Free PMC article.
PGC-1alpha as modifier of onset age in Huntington disease.
Taherzadeh-Fard E, Saft C, Andrich J, Wieczorek S, Arning L.
Taherzadeh-Fard E, et al.
Mol Neurodegener. 2009 Feb 6;4:10. doi: 10.1186/1750-1326-4-10.
Mol Neurodegener. 2009.
PMID: 19200361
Free PMC article.
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Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease.
Arning L, Haghikia A, Taherzadeh-Fard E, Saft C, Andrich J, Pula B, Höxtermann S, Wieczorek S, Akkad DA, Perrech M, Gold R, Epplen JT, Chan A.
Arning L, et al. Among authors: taherzadeh fard e.
J Mol Med (Berl). 2010 Apr;88(4):431-6. doi: 10.1007/s00109-010-0589-2. Epub 2010 Jan 29.
J Mol Med (Berl). 2010.
PMID: 20108082
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Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1.
Taherzadeh-Fard E, Saft C, Wieczorek S, Epplen JT, Arning L.
Taherzadeh-Fard E, et al.
Neurogenetics. 2010 Oct;11(4):435-9. doi: 10.1007/s10048-010-0248-3. Epub 2010 May 30.
Neurogenetics. 2010.
PMID: 20512606
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Novel cause of hereditary obstructive azoospermia: a T2 allele in the CFTR gene.
Radpour R, Taherzadeh-Fard E, Gourabi H, Aslani S, Vosough Dizaj A, Aslani A.
Radpour R, et al. Among authors: taherzadeh fard e.
Reprod Biomed Online. 2009 Mar;18(3):327-32. doi: 10.1016/s1472-6483(10)60089-2.
Reprod Biomed Online. 2009.
PMID: 19298730
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The Iranian human mutation database.
Motazacker MM, Taherzadeh-Fard E, Husseini Z, Behjati F, Esteghamat F, Kahrizi K, Najmabadi H.
Motazacker MM, et al. Among authors: taherzadeh fard e.
Arch Iran Med. 2007 Jul;10(3):372-5.
Arch Iran Med. 2007.
PMID: 17604476
No abstract available.
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