HERTZ
发表于 2025-3-23 12:50:04
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d-limonene
发表于 2025-3-23 14:31:16
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iodides
发表于 2025-3-23 19:12:01
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昏暗
发表于 2025-3-23 23:44:33
Oberes Sprunggelenk — Spezieller Teiled by premature onset of age-related phenotypic changes (such as cataract and greying of hair etc) and genome instability. Cells derived from CS patients are defective in DNA repair, and CS patients display severe neurological abnormalities and certain features of premature aging. The accelerated ag
insurgent
发表于 2025-3-24 05:37:31
Oberes Sprunggelenk — Allgemeiner Teilpress illegitimate recombination, particularly during the repair of DNA double strand breaks. Five . family genes have been identified in humans, and three (., and .) have been identified as defective in the human genetic disorders; Bloom syndrome, Werner syndrome, and a subset of Rothmund-Thomson s
开始发作
发表于 2025-3-24 10:15:41
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重叠
发表于 2025-3-24 12:12:42
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BOOR
发表于 2025-3-24 16:47:37
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越自我
发表于 2025-3-24 22:09:13
https://doi.org/10.1007/978-3-642-31322-6ility and DNA repair pathways that have evolved in the human genome to prevent the harmful effects of exposure to DNA damaging agents. One such disorder is Fanconi Anemia, an autosomal recessive disease characterized by an increased spontaneous and DNA cross-linkers induced chromosome instability, p
Arable
发表于 2025-3-25 01:04:03
https://doi.org/10.1007/978-3-642-31322-6langiectasia, immunodeficiency, chromosomal instability and radio sensitivity with an increased predisposition to lymphoid cancer in childhood. The gene responsible for AT, ataxia telangiectasia mutated (ATM), has been cloned and its protein product has been biochemically characterized as a serine/t