摘要:
A genetic method to kill cancer by suffocation is presented. The invention involves directly administering a bacterial plasmid in the form of an expression vector to cancer cells or tissue in a patient with cancerous growth. The plasmid is in the form of an expression vector with a nucleic acid encoding the silk protein gene.
摘要:
The present invention relates to methods of treating or preventing complement mediated neurodevelopmental disorders secondary to maternal infection with Zika virus, comprising administering to a pregnant female or to a foetus or embryo, a therapeutically or prophylactically effective amount of an agent which is a protein comprising amino acids 19 to 168 of the amino acid sequence in Figure 2 (SEQ ID NO: 2) or a functional equivalent of this protein.
摘要翻译:本发明涉及治疗或预防继发于母体寨卡病毒感染的补体介导的神经发育病症的方法,其包括向怀孕女性或胎儿或胚胎施用治疗或预防有效量的 包含图2(SEQ ID NO:2)中的氨基酸序列的氨基酸19至168或该蛋白质的功能等同物的蛋白质的试剂。 p>
摘要:
A method of using Shilajit or its individual components, or a combination of two or more of these components, to induce the body of a mammal, including that of a human, to synthesize new collagen and the related extracellular matrix proteins, thus promoting the health of all of the tissues and organs containing collagen and the related extracellular matrix proteins, including skin, connective tissue, muscle, cartilage, bone, and teeth and improve muscle building and regeneration, and/or treat collagen-related disorders is presented.
摘要:
Nutritive polypeptides are provided herein. Also provided are various other embodiments including nucleic acids encoding the polypeptides, recombinant microorganisms that make the polypeptides, vectors for expressing the polypeptides, methods of making the polypeptides using recombinant microorganisms, compositions and formulations that comprise the polypeptides, and methods of using the polypeptides, compositions and formulations.
摘要:
Nutritive polypeptides are provided herein. Also provided are various other embodiments including nucleic acids encoding the polypeptides, recombinant microorganisms that make the polypeptides, vectors for expressing the polypeptides, methods of making the polypeptides using recombinant microorganisms, compositions and formulations that comprise the polypeptides, and methods of using the polypeptides, compositions and formulations.
摘要:
The present invention provides methods for the inhibition of reperfusion injury by treatment with Grammastola spatulata mechanotoxin4 (GsMTx4). The GsMTx4 may be delivered to the ischemic tissue in an individual by any means prior to, during or after ischemia reperfusion injury.
摘要:
Nutritive polypeptides are provided herein. Also provided are various other embodiments including nucleic acids encoding the polypeptides, recombinant microorganisms that make the polypeptides, vectors for expressing the polypeptides, methods of making the polypeptides using recombinant microorganisms, compositions and formulations that comprise the polypeptides, and methods of using the polypeptides, compositions and formulations.
摘要:
An isolated and purified nucleic acid molecule that encodes a polypeptide comprising at least eight contiguous amino acids of SEQ ID NO: 1, 2, or 3, wherein the at least eight contiguous amino acids have anti-viral activity, as well as an isolated and purified nucleic acid molecule that encodes a polypeptide comprising at least eight contiguous amino acids of SEQ ID NO: 1, 2, or 3, wherein the at least eight contiguous amino acids have anti-viral activity, a vector comprising such an isolated and purified nucleic acid molecule, a host cell comprising the nucleic acid molecule, optionally in the form of a vector, a method of producing an anti-viral polypeptide or conjugate thereof, the anti-viral polypeptide itself, a conjugate or fusion protein comprising the anti-viral polypeptide, and compositions comprising an effective amount of the anti-viral polypeptide or conjugate or fusion protein thereof. Further provided are methods of inhibiting prophylactically or therapeutically a viral infection of a host.
摘要翻译:分离和纯化的核酸分子,其编码包含SEQ ID NO:1,2或3的至少8个连续氨基酸的多肽,其中所述至少8个连续氨基酸具有抗病毒活性,以及分离和 纯化的核酸分子,其编码包含SEQ ID NO:1,2或3的至少8个连续氨基酸的多肽,其中所述至少8个连续氨基酸具有抗病毒活性,包含这种分离和纯化的核酸的载体 酸分子,包含核酸分子的宿主细胞,任选以载体的形式,产生抗病毒多肽或其缀合物的方法,抗病毒多肽本身,包含抗病毒的缀合物或融合蛋白 多肽和包含有效量的抗病毒多肽或其结合物或其融合蛋白的组合物。 还提供了预防性或治疗性地抑制宿主的病毒感染的方法。
摘要:
Depot formulations including therapeutic proteins are provided. The therapeutic proteins can be toxin-based therapeutic proteins. The depot formulations release the therapeutic protein within sustained effective levels for at least one month following a single administration. The toxin-based therapeutic proteins can include ShK-based proteins.
摘要:
The present invention relates to methods, compositions, and devices for the transdermal delivery of therapeutic agents and cosmetic agents in inclusion body form. Such inclusion bodies can deliver therapeutic and cosmetic agents through the skin barrier and reach locations deep in the skin. The disclosed compositions can be used to treat skins diseases and conditions.