Barely Significant
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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease.

Mol Neurodegener · 2011 · PMC3117738 · PMID 21595933

Europe PMCDOI
2
hedged sentences
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp < 0.0001actually significant
Results In our cohort of 401 HD patients, the expanded HTT allele accounts for nearly 73% of the variance in motor AO (R 2 = 0.729) and shows a highly significant influence on the AO (p < 0.0001).

also in 132,142 other papers

nominally significantno p-value reported
Results In over 400 German HD patients, polymorphisms in the nuclear respiratory factor 1 gene, NRF-1 , and the mitochondrial transcription factor A, encoded by TFAM showed nominally significant association with AO of HD.

also in 7,732 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.