Showing 1 - 20 results of 36,493 for search '(( _ large decrease ) OR ((( via ((teer decrease) OR (_ decrease)) ) OR ( a rare increased ))))', query time: 0.85s Refine Results
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    DataSheet3_Coprophagy Prevention Decreases the Reproductive Performance and Granulosa Cell Apoptosis via Regulation of CTSB Gene in Rabbits.docx by Guohua Song (5152595)

    Published 2022
    “…Overexpression of CTSB increased secretion of progesterone and estradiol, partly via upregulation of CYP19A1 while inhibition of CTSB decreased progesterone secretion partly via downregulation of the StAR gene. …”
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    DataSheet2_Coprophagy Prevention Decreases the Reproductive Performance and Granulosa Cell Apoptosis via Regulation of CTSB Gene in Rabbits.ZIP by Guohua Song (5152595)

    Published 2022
    “…Overexpression of CTSB increased secretion of progesterone and estradiol, partly via upregulation of CYP19A1 while inhibition of CTSB decreased progesterone secretion partly via downregulation of the StAR gene. …”
  16. 16

    DataSheet1_Coprophagy Prevention Decreases the Reproductive Performance and Granulosa Cell Apoptosis via Regulation of CTSB Gene in Rabbits.ZIP by Guohua Song (5152595)

    Published 2022
    “…Overexpression of CTSB increased secretion of progesterone and estradiol, partly via upregulation of CYP19A1 while inhibition of CTSB decreased progesterone secretion partly via downregulation of the StAR gene. …”
  17. 17

    A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease by Gavin R. Oliver (7456514)

    Published 2019
    “…<div><p>Background</p><p>RNA sequencing has been proposed as a means of increasing diagnostic rates in studies of undiagnosed rare inherited disease. …”
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    A Rare Variant in Metallothionein 1E Increases the Risk for Type 2 Diabetes in a Chinese Population by Xiantong Zou (16861311)

    Published 2023
    “…</p><p dir="ltr">Results: Our analysis revealed a rare variant of the metallothionein 1E (MT1E) gene, p.C36Y, in a three-generation family with diabetes. …”
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    Table_1_A Rare KIF1A Missense Mutation Enhances Synaptic Function and Increases Seizure Activity.docx by Yi Guo (35817)

    Published 2020
    “…Ala397Asp) in KIF1A. Whole-cell recordings from primary cultured neurons revealed that the mutant KIF1A increases the excitatory synaptic transmission but not the intrinsic excitability of neurons, and phenotype testing in zebrafish showed that this rare mutation results in epileptic seizure-like activity. …”