Non-invasive prenatal genetic diagnosis using transcervical cells
    32.
    发明申请
    Non-invasive prenatal genetic diagnosis using transcervical cells 审中-公开
    非侵入性产前遗传诊断使用宫颈癌细胞

    公开(公告)号:US20040197832A1

    公开(公告)日:2004-10-07

    申请号:US10405698

    申请日:2003-04-03

    Abstract: A method is provided for determining the gender and/or chromosomal abnormality, e.g. chromosomal aneuploidy of a fetus comprising identifying fetal cells in a transcervical cell sample obtained from a pregnant woman, for example with an antibody specific to the HLA-G antigen expressed only by extravillous trophoblast cells, and then subjecting the identified fetal cells to fluorescence in situ hybridization (FISH) with one or more probes for detecting the sex of the fetus or a chromosomal abnormality such as a monosomy, a trisomy or a polyploidy, e.g. triploidy.

    Abstract translation: 提供了一种用于确定性别和/或染色体异常的方法,例如, 胎儿的染色体非整倍性包括鉴定从孕妇获得的子宫颈细胞样品中的胎儿细胞,例如用仅由绒毛滋养层细胞表达的HLA-G抗原特异的抗体,然后使鉴定的胎儿细胞在原位荧光 杂交(FISH)与一个或多个用于检测胎儿性别的探针或染色体异常如单体,三体或多倍体,例如 三倍体

    METHODS FOR TREATING DIEASES ASSOCIATED WITH IMPAIRED MEVALONATE PRODUCTION

    公开(公告)号:US20240342134A1

    公开(公告)日:2024-10-17

    申请号:US18682201

    申请日:2022-08-09

    CPC classification number: A61K31/366 A61K9/0053 A61P21/00

    Abstract: The use of mevalonolactone is provided for treating, preventing or alleviating diseases, disorders or conditions associated, directly or indirectly, with reduced mevalonic acid production in the mevalonate pathway, for example, due to damaged or hindered HMG CoA-reductase enzyme. Oral administration of mevalonolactone is provided for treating muscle cell and/or tissue damage caused at least in part due to impaired mevalonic acid production, as effected in diseases and disorders such as myopathy, statin-associated muscle symptom (SAMS), immune-mediated necrotizing myopathy (IMNM), rhabdomyolysis, muscular toxicity syndrome, myalgia, sarcopenia, and limb girdle muscular dystrophy (LGMD).

    EEG microstates analysis
    34.
    发明授权

    公开(公告)号:US12042293B2

    公开(公告)日:2024-07-23

    申请号:US16650875

    申请日:2018-09-21

    CPC classification number: A61B5/369 A61B5/165 A61B5/4088 A61B5/4842 A61B5/7275

    Abstract: Using microstate data to evaluate Alzheimer's disease including dementia and/or mild cognitive impairment and/or depression and optionally provide treatment based on the diagnosis and/or modify treatment and/or diagnosis based on response to treatment, optionally as measured using microstate data. In one example, the method includes analyzing EEG data to generate one or more EEG parameter; and generating a risk for one or both of depression and MCI (mild cognitive impairment) based on said one or more EEG parameters. Optionally, the disease comprises MCI. Optionally, the disease comprises depression. Optionally, the one or more EEG parameter comprises a microstate-derived parameter. Optionally, the one or more EEG parameter comprises a microstate duration derived parameter.

    MITOCHONDRIAL TRANSPLANTATION AND USE THEREOF IN OCULAR DISEASES

    公开(公告)号:US20220168358A1

    公开(公告)日:2022-06-02

    申请号:US17594141

    申请日:2020-04-03

    Abstract: Methods for treatment of ocular diseases and conditions associated with mitochondrial dysfunction, mitochondrial destruction and/or mitochondrial depletion in the eye, are disclosed. These methods comprise the transplantation of viable exogenous, isolated mitochondria to ocular tissues. Mitochondrial transplantation is effective in treatment of, e.g., an ocular manifestation of a disease or disorder in a subject, an ophthalmic disease, disorder or condition associated with mitochondrial dysfunction, and/or an ocular ischemic insult in a subject.

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