The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

7 citing papers in PubMed, 19 citations in OpenAlex.

1. Molecular genetics of the mammalian NADH-ubiquinone oxidoreductase.Journal of bioenergetics and biomembranes · 2001
   Review
2. Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain.Journal of inherited metabolic disease · 2001
   Article
3. The NDUFA1 gene product (MWFE protein) is essential for activity of complex I in mammalian mitochondria.Proceedings of the National Academy of Sciences of the United States of America · 1999
   Article
4. The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathology.Journal of inherited metabolic disease · 1999
   Article
5. The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients.Journal of inherited metabolic disease · 1999
   Article
6. The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.American journal of human genetics · 1998
   Article
7. Human mitochondrial transmembrane metabolite carriers: tissue distribution and its implication for mitochondrial disorders.Journal of bioenergetics and biomembranes · 1998
   Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

9 authors at 1 institution in 1 country.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as