aprataxin造句

例句与造句

  1. Ataxia oculomotor apraxia-1 is a neurological disorder caused by mutations in the APTX gene that encodes aprataxin.
  2. Mutations in the gene APTX, which encodes for aprataxin, have been identified to be responsible for AOA1.
  3. Aprataxin removes AMP from DNA ends following abortive ligation attempts by DNA Ligase IV during non-homologous end joining, thereby permitting subsequent attempts at ligation.
  4. Deficiencies in aprataxin, a phosphodiesterase responsible for reconditioning the DNA ( after DNA ligase I aborts the adenylylated DNA intermediate ), has been linked to neurodegeneration.
  5. Aprataxin ( a phosphodiesterase ) has been shown to act on aborted DNA intermediates via hydrolysis of the AMP-phosphate bond, restoring the DNA to its initial state before the ligase had reacted.
  6. It's difficult to find aprataxin in a sentence. 用aprataxin造句挺难的
  7. The second linker interacts with polynucleotide kinase phosphatase ( PNKP ) ( that processes DNA broken ends during base excision repair ), aprataxin ( active in single-strand DNA repair and non-homologous end joining ) and a third protein designated aprataxin-and PNKP-like factor.
  8. The second linker interacts with polynucleotide kinase phosphatase ( PNKP ) ( that processes DNA broken ends during base excision repair ), aprataxin ( active in single-strand DNA repair and non-homologous end joining ) and a third protein designated aprataxin-and PNKP-like factor.
  9. In cases where the distinction is unclear, clinical laboratories can identify genetic abnormalities of ATM, aprataxin and senataxin, and specialty centers can identify abnormality of the proteins of potentially responsible genes, such as ATM, MRE11, nibrin, TDP1, aprataxin and senataxin as well as other proteins important to ATM function such as ATR, DNA-PK, and RAD50.
  10. In cases where the distinction is unclear, clinical laboratories can identify genetic abnormalities of ATM, aprataxin and senataxin, and specialty centers can identify abnormality of the proteins of potentially responsible genes, such as ATM, MRE11, nibrin, TDP1, aprataxin and senataxin as well as other proteins important to ATM function such as ATR, DNA-PK, and RAD50.

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