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[HTML][HTML] Machine learning-based approach highlights the use of a genomic variant profile for precision medicine in ovarian failure
I Henarejos-Castillo, A Aleman… - Journal of Personalized …, 2021 - mdpi.com
Ovarian failure (OF) is a common cause of infertility usually diagnosed as idiopathic, with
genetic causes accounting for 10–25% of cases. Whole-exome sequencing (WES) may …
genetic causes accounting for 10–25% of cases. Whole-exome sequencing (WES) may …
Chromosome-Level Genome Assembly Provides Insights into the Evolution of the Special Morphology and Behaviour of Lepturacanthus savala
RX Wu, BB Miao, FY Han, SF Niu, YS Liang, ZB Liang… - Genes, 2023 - mdpi.com
Savalani hairtail Lepturacanthus savala is a widely distributed fish along the Indo-Western
Pacific coast, and contributes substantially to trichiurid fishery resources worldwide. In this …
Pacific coast, and contributes substantially to trichiurid fishery resources worldwide. In this …
[HTML][HTML] Болезнь Гентингтона
СА Клюшников - Неврологический журнал имени ЛО Бадаляна, 2020 - cyberleninka.ru
Болезнь Гентингтона (БГ) является одним из наиболее частых наследственных
нейродегенеративных заболеваний. БГ практически инкурабельна, неизбежно …
нейродегенеративных заболеваний. БГ практически инкурабельна, неизбежно …
Huntington disease gene expression signatures in blood compared to brain of YAC128 mice as candidates for monitoring of pathology
While the genetic cause of Huntington disease (HD) is known since 1993, still no cure exists.
Therapeutic development would benefit from a method to monitor disease progression and …
Therapeutic development would benefit from a method to monitor disease progression and …
DYNLT1 gene expression is downregulated in whole blood of patients at different Huntington's disease stages
SM Rosseto, TA Alarcon, DMC Rocha, FM Ribeiro… - Neurological …, 2021 - Springer
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG nucleotide
expansion, which encodes the amino acid glutamine, in the huntingtin gene. HD is …
expansion, which encodes the amino acid glutamine, in the huntingtin gene. HD is …
Genome variant characterization, population stratification, and systemic analysis for precision medicine in patients with ovarian failure
I Henarejos Castillo - 2024 - roderic.uv.es
Ovarian failure is a complex and multifactorial disorder usually characterized by an
accelerated depletion of the follicular reserve before the age of natural menopause in …
accelerated depletion of the follicular reserve before the age of natural menopause in …
Huntington's disease
SA Klyushnikov - LO Badalyan Neurological Journal, 2020 - journals.eco-vector.com
Huntington's disease is one of the most common hereditary neurodegenerative diseases,
which remains practically incurable, inevitably leading to the disability of patients and …
which remains practically incurable, inevitably leading to the disability of patients and …