Search Results - "Chartois, Frédérique"
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A new frontier in Fanconi anemia: From DNA repair to ribosome biogenesis
Published in Blood reviews (01-03-2022)“…Described by Guido Fanconi almost 100 years ago, Fanconi anemia (FA) is a rare genetic disease characterized by developmental abnormalities, bone marrow…”
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Contribution of p53-dependent and -independent mechanisms to upregulation of p21 in Fanconi anemia
Published in PLoS genetics (07-11-2024)“…Abnormal expression of the cell cycle inhibitor and p53 target CDKN1A /p21 has been associated with paradoxical outcomes, such as hyperproliferation in…”
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Fanconi anemia A protein participates in nucleolar homeostasis maintenance and ribosome biogenesis
Published in Science advances (01-01-2021)“…Fanconi anemia (FA), the most common inherited bone marrow failure and leukemia predisposition syndrome, is generally attributed to alterations in DNA damage…”
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Fanca deficiency is associated with alterations in osteoclastogenesis that are rescued by TNFα
Published in Cell & bioscience (24-06-2023)“…Hematopoietic stem cells (HSCs) reside in the bone marrow (BM) niche, which includes bone-forming and bone-resorbing cells, i.e., osteoblasts (OBs) and…”
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Amyrel, a paralogous gene of the amylase gene family in Drosophila melanogaster and the Sophophora subgenus
Published in Proceedings of the National Academy of Sciences - PNAS (09-06-1998)“…We describe a gene from Drosophila melanogaster related to the alpha-amylase gene Amy. This gene, which exists as a single copy, was named Amyrel. It is…”
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Fanca deficiency is associated with alterations in osteoclastogenesis that are rescued by TNF[alpha]
Published in Cell & bioscience (24-06-2023)“…Hematopoietic stem cells (HSCs) reside in the bone marrow (BM) niche, which includes bone-forming and bone-resorbing cells, i.e., osteoblasts (OBs) and…”
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Evidence of a high rate of selective sweeps in African Drosophila melanogaster
Published in Genetics (Austin) (01-02-2003)“…Assessing the rate of evolution depends on our ability to detect selection at several genes simultaneously. We summarize DNA sequence variation data in three…”
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