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33results about How to "Enhance mobilization" patented technology

Therapeutic, fitness, and sports enhancement device

A therapeutic, fitness, and sports enhancement device comprising a cylindrically shaped body having a predetermined density and predetermined diameter including a plurality of projections of a predetermined shape. One or more of the predetermined density, the predetermined diameter, and predetermined shape are configured to enhance mobilization of one or more small soft tissue structures of the human body.
Owner:PERFORMANCE SOLUTIONS

DME Fracing

InactiveUS20170218260A1Enhance mobilizationIncreasing gas and oil saturationFluid removalDrilling compositionChemistryEther
Herein is described a frac fluid comprising of di-methyl ether (DME) or a mixture of DME and propane to be used in hydraulic fracturing of underground formations.
Owner:CHAKRABARTY NEILIN

Dislodgement and release of hsc from the bone marrow stem cell niche using alpha9 integrin antagonists

InactiveUS20170348375A1Altered susceptibilityLonger treatmentOrganic active ingredientsNervous disorderBone Marrow Stem CellHaematological disorders
Haematopoietic stem cell mobilization is a process whereby haematopoietic stem cells are stimulated out of the bone marrow space. Before HSC can mobilize, they must be dislodged and released from the BM stem cell niche in which they reside and are retained by adhesive interactions. Accordingly, in an aspect of the present invention there is provided a method for enhancing dislodgement of HSC and their precursors and progenitors thereof from a BM stem cell binding ligand in vivo or ex vivo, said method comprising administering in vivo or ex vivo an effective amount of an antagonist of an a 9 integrin or an active portion thereof to the BM stem cell niche. Once mobilized to the peripheral blood (PB) the HSC may be collected for transplant. Methods which enhance mobilization of the HSC can also improve treatments of haematological disorders.
Owner:COMMONWEALTH SCI & IND RES ORG

Methods and products for manipulating hematopoietic stem cells

InactiveUS20080057579A1Enhance mobilizationEnhance transmigrationCell receptors/surface-antigens/surface-determinantsPeptide/protein ingredientsBone marrow derived hematopoietic stem cellStem Cell Protein
The invention relates to methods for manipulating hematopoietic stem cells and related products. In one aspect the invention relates to the use of stem cell G-protein coupled receptor (SC-GPR) related compositions to identify bone marrow derived hematopoietic stem cells, to enhance mobilization of hematopoietic stem cells, to improve the efficiency of targeting cells to the bone marrow and / or to modulate hematopoietic cell function.
Owner:THE GENERAL HOSPITAL CORP

Bifunctional vectors allowing bcl11a silencing and expression of an Anti-sickling hbb and uses thereof for gene therapy of b-hemoglobinopathies

The #β-hemoglobinopathies #β-thalassemia (BT) and sickle cell disease (SCD) are the most frequent genetic disorders worldwide. These diseases are caused by mutations causing reduced or abnormal synthesis of the β-globin chain of the adult hemoglobin (Hb) tetramer. Here, the inventors intend to improve HSC-based gene therapy for β-thalassemia and SCD by developing an innovative, highly infectious LV vector expressing a potent anti-sickling β-globin transgene and a second biological function either increasing fetal γ-globin expression (for β-thalassemia and SCD). More particularly, the inventors have designed a novel lentivirus (LV), which carry two different functions: βAS3 gene addition and gene silencing. This last strategy allows the re-expression of the fetal γ-globin genes (HBG1 and HBG2) and production of the endogenous fetal hemoglobin (HbF). Elevated levels of HbF and HbAS3 (Hb tetramer containing βAS3-globin) will benefit the β-hemoglobinopathy phenotype by increasing the total amount of β-like globin that will: (i) reduce the alpha precipitates and improve the alpha/non alpha ratio in β-thalassemia, and (ii) reduce the sickling in SCD. This combined strategy will improve the β-hemoglobinopathy phenotype at a lower vector copy number (VCN) per cell compared to a LV expressing the βAS3 alone.
Owner:INST NAT DE LA SANTE & DE LA RECHERCHE MEDICALE (INSERM) +4
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