WO2006067254A3 - MÉTODO Y DISPOSITIVO IN VITRO DE DIAGNÓSTICO DE LA HIPERCOLESTEROLEMIA FAMILIAR BASADO EN LA DETECCIÓN DE MUTACIONES EN LA SECUENCIA DEL GEN DEL RECEPTOR DE LIPOPROTEÍNAS DE BAJA DENSIDAD (r-LDL) - Google Patents

MÉTODO Y DISPOSITIVO IN VITRO DE DIAGNÓSTICO DE LA HIPERCOLESTEROLEMIA FAMILIAR BASADO EN LA DETECCIÓN DE MUTACIONES EN LA SECUENCIA DEL GEN DEL RECEPTOR DE LIPOPROTEÍNAS DE BAJA DENSIDAD (r-LDL) Download PDF

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Publication number
WO2006067254A3
WO2006067254A3 PCT/ES2005/070160 ES2005070160W WO2006067254A3 WO 2006067254 A3 WO2006067254 A3 WO 2006067254A3 ES 2005070160 W ES2005070160 W ES 2005070160W WO 2006067254 A3 WO2006067254 A3 WO 2006067254A3
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WO
WIPO (PCT)
Prior art keywords
mutations
low
density lipoprotein
lipoprotein receptor
familial hypercholesterolemia
Prior art date
Application number
PCT/ES2005/070160
Other languages
English (en)
French (fr)
Other versions
WO2006067254A2 (es
Inventor
Mieras Miguel Pocovi
Hernandez Diego Tejedor
Fernandez Sergio Castillo
Perez Miguel Mallen
Martinez Antonio Martinez
Original Assignee
Lacer Sa
Mieras Miguel Pocovi
Hernandez Diego Tejedor
Fernandez Sergio Castillo
Perez Miguel Mallen
Martinez Antonio Martinez
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lacer Sa, Mieras Miguel Pocovi, Hernandez Diego Tejedor, Fernandez Sergio Castillo, Perez Miguel Mallen, Martinez Antonio Martinez filed Critical Lacer Sa
Publication of WO2006067254A2 publication Critical patent/WO2006067254A2/es
Publication of WO2006067254A3 publication Critical patent/WO2006067254A3/es

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/156—Polymorphic or mutational markers

Abstract

Certificado de adición a la patente 200300206 para un: Procedimiento y Dispositivo de Detección de Mutaciones en Secuencias Génicas Aisladas del Receptor de Lipoproteínas de Baja Densidad (r-LDL) asociado con la Hipercolesterolemia Familiar. La invención describe métodos extracorpóreos para analizar la presencia o ausencia de doce mutaciones causantes de hipercolesterolemia familiar. Los métodos indican la forma de detectar estas mutaciones a partir de una muestra de ADN de un individuo y utilizando la reacción en cadena de la polimerasa con cebadores complementarios al gen del receptor de las lipoproteínas de baja densidad, el análisis del producto amplificado por secuenciación, análisis de restricción, técnicas de los polimorfismos de conformación de cadena sencilla, análisis de heterodúplex y de un dispositivo sobre un soporte de vidrio 'biochip' en el que se depositan sondas oligonucleotídicas que permiten detectar estas doce mutaciones en el ADN.
PCT/ES2005/070160 2004-12-21 2005-11-23 MÉTODO Y DISPOSITIVO IN VITRO DE DIAGNÓSTICO DE LA HIPERCOLESTEROLEMIA FAMILIAR BASADO EN LA DETECCIÓN DE MUTACIONES EN LA SECUENCIA DEL GEN DEL RECEPTOR DE LIPOPROTEÍNAS DE BAJA DENSIDAD (r-LDL) WO2006067254A2 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ES200403041 2004-12-21
ESP200403041 2004-12-21

Publications (2)

Publication Number Publication Date
WO2006067254A2 WO2006067254A2 (es) 2006-06-29
WO2006067254A3 true WO2006067254A3 (es) 2006-11-02

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PCT/ES2005/070160 WO2006067254A2 (es) 2004-12-21 2005-11-23 MÉTODO Y DISPOSITIVO IN VITRO DE DIAGNÓSTICO DE LA HIPERCOLESTEROLEMIA FAMILIAR BASADO EN LA DETECCIÓN DE MUTACIONES EN LA SECUENCIA DEL GEN DEL RECEPTOR DE LIPOPROTEÍNAS DE BAJA DENSIDAD (r-LDL)

Country Status (1)

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WO (1) WO2006067254A2 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0922377D0 (en) * 2009-12-22 2010-02-03 Arab Gulf University The Mutant LDL receptor
CN102718870B (zh) * 2011-05-24 2014-04-30 马鞍山中美德康生物科技有限公司 一种胰岛素生物增敏剂及其应用
CA2926218A1 (en) 2013-10-03 2015-04-09 Moderna Therapeutics, Inc. Polynucleotides encoding low density lipoprotein receptor

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4966837A (en) * 1984-12-28 1990-10-30 Board Of Regents, The University Of Texas System Methods and compositions for the detection of familial hypercholesterolemia
WO2002006467A1 (fr) * 2000-07-18 2002-01-24 Bml, Inc. Methode de detection d'erreurs du metabolisme lipidique

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4966837A (en) * 1984-12-28 1990-10-30 Board Of Regents, The University Of Texas System Methods and compositions for the detection of familial hypercholesterolemia
WO2002006467A1 (fr) * 2000-07-18 2002-01-24 Bml, Inc. Methode de detection d'erreurs du metabolisme lipidique

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
FOUCHIER S.W. ET AL.: "The molecular basis of familial hypercholesterolemia in the Netherlands", HUMAN GENETICS, vol. 109, no. 6, December 2001 (2001-12-01), pages 602 - 615, XP002980736, DOI: doi:10.1007/s00439-001-0628-8 *
LIND S. ET AL.: "Genetic characterization of Swedish patients with familial hypercholesterolemia. A heterogenous pattern of mutations in the LDL receptor gene", ATHEROSCLEROSIS, vol. 163, no. 2, August 2002 (2002-08-01), pages 399 - 407 *
MOZAS P. ET AL.: "Molecular characterization of familial hypercholesterolemia in Spain: identification of 39 novel and 77 recurrent mutations in LDLR", HUM. MUTAT., vol. 24, no. 2, August 2004 (2004-08-01), pages 187, XP055134966, DOI: doi:10.1002/humu.9264 *
PISCIOTTA LIVIA ET AL.: "A "de novo" mutation of the LDL receptor gene as the cause of familial hypercholesterolemia", BIOCHIMIA ET BIOPHYSICA ACTA, vol. 1587, no. 1, 21 May 2002 (2002-05-21), pages 7 - 11, XP004354397, DOI: doi:10.1016/S0925-4439(02)00047-9 *
VARRET M. ET AL.: "Results of the molecular analysis of the 220 point mutations in the human LDL receptor gene database", ATHEROSCLEROSIS, vol. 134, no. 1-2, October 1997 (1997-10-01), pages 74, XP002980738, DOI: doi:10.1016/S0021-9150(97)88454-7 *

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