Berta
Berta Alquezar García, La Eliana, Valencia ES
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20120272405 | REPELLENT COMPOSITIONS AND GENETIC APPROACHES FOR CONTROLLING HUANGLONGBING - The invention provides a method for controlling Huanglongbing (HLB) disease of citrus plants through expressing genes encoding synthases for sesquiterpenes such as β-caryophyllene, and α-copaene, and combinations thereof, in citrus plants. Methods of controlling HLB comprising applying at least one purified sesquiterpene, which repels | 10-25-2012 |
Berta Alquezar GarcÍa, La Eliana (valencia) ES
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20150353954 | REPELLENT COMPOSITIONS AND GENETIC APPROACHES FOR CONTROLLING HUANGLONGBING - The invention provides a method for controlling Huanglongbing (HLB) disease of citrus plants through expressing genes encoding synthases for sesquiterpenes such as β-caryophyllene, and α-copaene, and combinations thereof, in citrus plants. Methods of controlling HLB comprising applying at least one purified sesquiterpene, which repels | 12-10-2015 |
20150353955 | REPELLENT COMPOSITIONS AND GENETIC APPROACHES FOR CONTROLLING HUANGLONGBING - The invention provides a method for controlling Huanglongbing (HLB) disease of citrus plants through expressing genes encoding synthases for sesquiterpenes such as β-caryophyllene, and α-copaene, and combinations thereof, in citrus plants. Methods of controlling HLB comprising applying at least one purified sesquiterpene, which repels | 12-10-2015 |
Berta Gomez De Pedraza, Hamburg DE
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20150367424 | Drilling Template, Drilling Template Arrangement And Method For Introducing Bores - A drilling template for use in the field of producing aircraft or spacecraft or parts thereof has a first template part and a second template part. The first template part and the second template part are in each case provided here with means for fixing positions of bores to be produced. The drilling template has coupling means, by which the first template part and the second template part can be coupled to one another in such a way that the coupled template parts are movable relative to one another. | 12-24-2015 |
Berta Kotar-Jordan, Kostanjevica Na Krki SI
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20090130205 | Solid Pharmaceutical Composition Comprising Donepezil Hydrochloride - The invention relates to a solid pharmaceutical composition comprising donepezil hydrochloride hydrate and a process for its preparation. In particular it relates to a composition and a process wherein the donepezil hydrochloride retains its polymorphic form and is therefore highly stable against conversion into other polymorphic forms. | 05-21-2009 |
20100317694 | Solid pharmaceutical composition comprising donepezil hydrochloride - The invention relates to a solid pharmaceutical composition comprising donepezil hydrochloride hydrate and a process for its preparation. In particular it relates to a composition and a process wherein the donepezil hydrochloride retains its polymorphic form and is therefore highly stable against conversion into other polymorphic forms. | 12-16-2010 |
20120283291 | SOLID PHARMACEUTICAL COMPOSITION COMPRISING DONEPEZIL HYDROCHLORIDE - The invention relates to a solid pharmaceutical composition comprising donepezil hydrochloride hydrate and a process for its preparation. In particular it relates to a composition and a process wherein the donepezil hydrochloride retains its polymorphic form and is therefore highly stable against conversion into other polymorphic forms. | 11-08-2012 |
Berta Levavi-Sivan, Rosh Haayin IL
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20150072933 | NOVEL SEQUENCES FOR THE CONTROL OF REPRODUCTION IN FISH - The present invention relates to novel peptide sequences, compositions and methods for controlling fish reproduction. More particularly, the invention provides novel Neurokinin B peptides NKF and NKB and analogues thereof that regulate reproduction in fish. The invention further provides preprohormone thereof comprising at least one of a first peptide fragment of the amino acid sequence X | 03-12-2015 |
Berta Ponsati Obiols, Gava-Barcelona ES
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20100021510 | NEURONAL EXOCYTOSIS INHIBITING PEPTIDES - The invention relates to peptides of general formula (I): | 01-28-2010 |
Berta Ponsati Obiols, Barcelona ES
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20110166071 | METHOD FOR SYNTHESIZING THYMOSINS - The invention relates to a method for obtaining thymosins and/or the pharmaceutically acceptable salts thereof by means of solid-phase synthesis on polymeric supports, which comprises the steps of linearly synthesizing the thymus-derived peptides in solid phase, incorporating at least one Thr or Ser in the sequence, in pseudoproline dipeptide form, obtaining the thymosins by treating the peptidyl resin with trifluoroacetic acid, and purifying the thymosins by RP-HPLC. The present invention also protects the isolated and/or purified compound obtained by means of said method and also the use thereof in the preparation of a medicinal product. | 07-07-2011 |
20120122781 | PEPTIDE LIGANDS OF SOMATOSTATIN RECEPTORS - Peptide derivatives, their stereoisomers, mixtures thereof and/or their pharmaceutically acceptable salts, a method of obtaining them, pharmaceutical compositions containing them and the use thereof for the treatment, prevention and/or diagnosis of those conditions, disorders and/or pathologies in which the sstr1, sstr2, sstr3, sstr4 and/or sstr5 somatostatin receptors are expressed. | 05-17-2012 |
20130172529 | METHOD FOR SYNTHESIZING THYMOSINS - The invention relates to a method for obtaining thymosins and/or the pharmaceutically acceptable salts thereof by means of solid-phase synthesis on polymeric supports, which comprises the steps of linearly synthesizing the thymus-derived peptides in solid phase, incorporating at least one Thr or Ser in the sequence, in pseudoproline dipeptide form, obtaining the thymosins by treating the peptidyl resin with trifluoroacetic acid, and purifying the thymosins by RP-HPLC. The present invention also protects the isolated and/or purified compound obtained by means of said method and also the use thereof in the preparation of a medicinal product. | 07-04-2013 |
20130210728 | TOPICAL OPHTHALMIC PEPTIDE FORMULATION - A topical ophthalmic formulation of peptides and their use for the treatment and/or local prevention of ocular diseases, preferably posterior segment eye diseases. | 08-15-2013 |
Berta Ponsati Obliols, Barcelona ES
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20110206752 | COMPOSITIONS FOR THE TREATMENT OF PAIN AND/OR INFLAMATION - Compositions for the treatment of pain and/or inflammation comprising at least one peptide with the general formula (I) R1-AA-R2, its stereoisomers, mixtures thereof, and its cosmetically and pharmaceutically acceptable salts. Peptide with general formula (I), its stereoisomers, mixtures thereof, and its cosmetically and pharmaceutically acceptable salts for the treatment of pain and/or inflammation. | 08-25-2011 |
Berta Rivas MundiÑa, Santiago De Compostela ES
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20160067023 | DEVICE FOR ENDODONTICS BY MEANS OF CONTINUOUS ULTRASONIC IRRIGATION - The invention relates to a device for endodontics by means of continuous ultrasonic irrigation with negative apical suction for the administration of disinfectants and other adjuvant substances in odontological treatment, comprising three fundamental parts: a plastic body connected to an ultrasonic dental unit, a coronal cannula for the ejection of the irrigant, and a microcannula that sucks up same. | 03-10-2016 |
Berta Rodes, Madrid ES
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20100047281 | VARIANTS OF HEPATITIS B VIRUS WITH RESISTANCE TO ANTI-VIRAL NUCLEOSIDE AGENTS AND APPLICATIONS THEREOF - The present invention relates generally to viral variants exhibiting reduced sensitivity to particular agents and/or reduced interactivity with immunological reagents. More particularly, the present invention is directed to hepatitis B virus (HBV) variants exhibiting complete or partial resistance to nucleoside or nucleotide analogs or other antagonists of HBV DNA polymerase activity and/or reduced interactivity with antibodies to viral surface components including reduced sensitivity to these antibodies. The present invention further contemplates assays for detecting such viral variants. These assays are useful in monitoring anti-viral therapeutic regimens and in developing new or modified vaccines directed against viral agents and in particular the resistant HBV variants of the present invention. The present invention also contemplates the use of the viral variants to screen for agents capable of inhibiting infection, replication and/or release of the virus. | 02-25-2010 |
Berta Strulovici, So. San Francisco, CA US
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20120122212 | TGF-BETA PATHWAY INHIBITORS FOR ENHANCEMENT OF CELLULAR REPROGRAMMING OF HUMAN CELLS - The present disclosure provides methods and compositions to enhance reprogramming in human cells. In some cases, the method includes contacting human cells with an inhibitor of the TGFβ pathway, for example a TGFβ receptor (TGFβR) inhibitor in combination with one or more induction factors. | 05-17-2012 |
Berta Vega Sanchaz, Koln DE
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20150259461 | SILANE FUNCTIONAL BINDER WITH THIOURETHANE STRUCTURE - The invention relates to a method for producing polyurethanes containing silane groups by reacting at least A) a composition containing a) one or more compounds containing isocyanate and silane groups of general formula (I) and b)<=1 percent by weight, relative to the total mass of composition A), one or more monomeric diisocyanates with aliphatically, cycloaliphatically, araliphatically and/or aromatically bonded isocyanate groups of general formula (II), where R1, R2 and R3 are the same or different radicals and respectively indicate a saturated or unsaturated, linear or branched, aliphatic or cycloaliphatic or an optionally substituted aromatic or araliphatic radical with up to 18 carbon atoms, which can contain optionally up to 3 heteroatoms from the series oxygen, sulphur, nitrogen, X is a linear or branched organic radical with at least 2 carbon atoms and Y is a linear or branched, aliphatic or cycloaliphatic radical with 4 to 18 carbon atoms or an optionally substituted aromatic or araliphatic radical with 6 to 18 carbon atoms, with B) an at least difunctional polyol with a numerically average molecular weight Mn of 62 to 22000 g/mol, preferably 90 to 12000 g/mol, while maintaining an equivalent ratio of isocyanate groups to hydroxyl groups of 0.7:1 to 1.2:1. The invention further relates to the products which can be obtained using the method according to the invention. Moreover, the invention relates to the use of the products which can be obtained using the method according to the invention as starting components in the production of cross-linkable binders, varnish, and raw materials for sealants or adhesives. | 09-17-2015 |
Berta Vega Sanchez, Koln DE
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20150175859 | ADHESIVE FORMULATIONS - The present invention relates to adhesive formulations based on uretdione-group-comprising polyaddition compounds that are free of isocyanate groups and monomeric polyisocyanates, and to the use thereof for the production of adhesive bonds between substrates, in particular for the production of flexible film composites. | 06-25-2015 |
20150203623 | BINDER WITH CYCLIC CARBONATE STRUCTURES - The invention relates to a method for producing polyurethanes containing cyclic carbonate structures by reacting at least A) a composition containing a) one or more compounds of the general formula (I), said compounds containing isocyanate groups and cyclic carbonate structures, and b) <=1 wt. %, based on the total mass of the composition A), of one or more monomer diisocyanates with aliphatically, cycloaliphatically, araliphatically, and/or aromatically bound isocyanate groups of the general formula (II), wherein R represents hydrogen or a saturated or unsaturated, linear or branched, aliphatic group with 1 to 7 carbon atoms, X represents a linear or branched organic group which comprises 1 to 36 carbon atoms and which can contain optionally ether, ester, and/or carbonate groups, n represents 0 or 1, and Y represents a linear or branched, aliphatic or cycloaliphatic group with 4 to 18 carbon atoms or an optionally substituted aromatic or aliphatic group with 6 to 18 carbon atoms, with B) an at least difunctional polyol with a number-average molecular weight Mn of 62 to 22000 g/mol, preferably 90 to 12000 g/mol, while maintaining an equivalent ratio of isocyanate groups to hydroxyl groups of 0.3:1 to 1.2:1. Furthermore, the invention relates to products which can be obtained using the method according to the invention. The invention additionally relates to the use of the products which can be obtained using the method according to the invention as a starting component in the production of crosslinkable binders, such as paints and raw materials for sealants or adhesives. | 07-23-2015 |