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EP1349963

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EP About this file: EP1349963

EP1349963 - METHOD FOR THE DETERMINATION OF AT LEAST ONE FUNCTIONAL POLYMORPHISM IN THE NUCLEOTIDE SEQUENCE OF A PRESELECTED CANDIDATE GENE AND ITS APPLICATIONS [Right-click to bookmark this link]
Status	The application is deemed to be withdrawn Status updated on 24.11.2006 Database last updated on 02.11.2024
Most recent event Tooltip	24.11.2006	Application deemed to be withdrawn	published on 27.12.2006 [2006/52]
Applicant(s)	For all designated states GenOdyssee Parc d'Affaires Technopolis, 3 avenue du Canada, Bat Alpha, B.P.810, Les Ulis 91974 Courtaboeuf / FR
	[N/P]
Former [2003/41]	For all designated states GenOdyssee Parc d'Affaires Technopolis, 3 avenue du Canada, Bat Alpha, B.P.810, Les Ulis 91974 Courtaboeuf / FR
Inventor(s)	01 / ESCARY, Jean-Louis 4 rue Moxouris F-78510 Le Chesnay / FR
	[2003/41]
Representative(s)	Santarelli Tour Trinity 1 bis Esplanade de la Défense 92035 Paris La Défense Cedex / FR
	[N/P]
Former [2003/41]	Santarelli 14, avenue de la Grande Armée, B.P. 237 75822 Paris Cedex 17 / FR
Application number, filing date	01999666.9	06.12.2001
	[2003/41]
	WO2001EP15427
Priority number, date	FR20000015838	06.12.2000 Original published format: FR 0015838
	[2003/41]
Filing language	EN
Procedural language	EN
Publication	Type:	A2 Application without search report
	No.:	WO0246459
	Date:	13.06.2002
	Language:	EN
	[2002/24]
	Type:	A2 Application without search report
	No.:	EP1349963
	Date:	08.10.2003
	Language:	EN
	The application published by WIPO in one of the EPO official languages on 13.06.2002 takes the place of the publication of the European patent application.
	[2003/41]
Search report(s)	International search report - published on:	EP	13.03.2003
Classification	IPC:	C12Q1/68, C07K14/52, C07K16/24	[2003/41]
	CPC:	C12Q1/6869 (EP,US); A61P31/12 (EP); A61P35/00 (EP)
	C-Set:	C12Q1/6869, C12Q2535/125 (EP,US)
Designated contracting states	AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LI, LU, MC, NL, PT, SE, TR [2003/41]
Extension states	AL	Not yet paid
	LT	Not yet paid
	LV	Not yet paid
	MK	Not yet paid
	RO	Not yet paid
	SI	Not yet paid
Title	German:	VERFAHREN ZUR BESTIMMUNG WENIGSTENS EINES FUNKTIONELLEN POLYMORPHISMUS IN DER NUKLEOTIDSEQUENZ EINES VORGEWÄHLTEN KANDIDATENGENS UND SEINE ANWENDUNGEN	[2003/41]
	English:	METHOD FOR THE DETERMINATION OF AT LEAST ONE FUNCTIONAL POLYMORPHISM IN THE NUCLEOTIDE SEQUENCE OF A PRESELECTED CANDIDATE GENE AND ITS APPLICATIONS	[2003/41]
	French:	PROCEDE DE DETERMINATION D'AU MOINS UN POLYMORPHISME FONCTIONNEL DANS LA SEQUENCE DES NUCLEOTIDES D'UN GENE CANDIDAT PRESELECTIONNE ET APPLICATIONS DUDIT PROCEDE	[2003/41]
Entry into regional phase	03.07.2003	National basic fee paid
	03.07.2003	Designation fee(s) paid
	03.07.2003	Examination fee paid
Examination procedure	04.07.2002	Request for preliminary examination filed International Preliminary Examining Authority: EP
	03.07.2003	Amendment by applicant (claims and/or description)
	03.07.2003	Examination requested [2003/41]
	04.07.2006	Application deemed to be withdrawn, date of legal effect [2006/52]
	07.08.2006	Despatch of communication that the application is deemed to be withdrawn, reason: renewal fee not paid in time [2006/52]
Fees paid	Renewal fee
	24.03.2003	Renewal fee patent year 03
	22.03.2004	Renewal fee patent year 04
	Penalty fee
	Additional fee for renewal fee
	31.12.2005	05 M06 Not yet paid
Opt-out from the exclusive Tooltip competence of the Unified Patent Court	See the Register of the Unified Patent Court for opt-out data
	Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Cited in	International search	[X]EP0626448 (BOEHRINGER INGELHEIM INT [DE]) [X] 17-20 * the whole document *;
		[X]WO9800541 (CHIRON CORP [US]) [X] 17-20 * the whole document *;
		[X]US5795976 (OEFNER PETER JOSEF [AT], et al) [X] 1-18 * the whole document *;
		[X]WO0051053 (GEMINI RESEARCH LTD [GB], et al) [X] 22-24 * the whole document *;
		[X]WO0066772 (CENTRE NAT RECH SCIENT [FR], et al) [X] 1-18 * the whole document *;
		[X] - CARGILL M ET AL, "Characterization of single-nucleotide polymorphisms in coding regions of human genes", NATURE GENETICS, NATURE AMERICA, NEW YORK, US, (199907), vol. 22, ISSN 1061-4036, pages 231 - 238, XP002121300 [X] 1-18 * the whole document * DOI: http://dx.doi.org/10.1038/10290
		[X] - LEE NANCY ET AL, "Interferon-alpha-2 variants in the human genome.", JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, (1995), vol. 15, no. 4, ISSN 1079-9907, pages 341 - 349, XP001016231 [X] 1-5,8,9,13,15,17,18 * the whole document *
		[X] - KITA MASAKAZU ET AL, "Determination of interferon-alpha-2 allele composition in the genomic DNA from healthy volunteers and leukemic patients in Japan.", JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, (1997), vol. 17, no. 3, ISSN 1079-9907, pages 135 - 140, XP001016233 [X] 1-5,8,9,13,15,17,18 * the whole document *
		[X] - MILLER-LINDHOLM A K ET AL, "A naturally occurring genetic variant in the human chorionic gonadotropin-beta gene 5 is assembly inefficient.", ENDOCRINOLOGY. UNITED STATES AUG 1999, (199908), vol. 140, no. 8, ISSN 0013-7227, pages 3496 - 3506, XP002218805 [X] 1-5,8,9,13,17,18 * the whole document * DOI: http://dx.doi.org/10.1210/en.140.8.3496
		[X] - VOSS T ET AL, "PERIPLASMIC EXPRESSION OF HUMAN INTERFERON-ALPHA2C IN ESCHERICHIA COLI RESULTS IN A CORRECTLY FOLDED MOLECULE", JOURNAL OF BIOCHEMISTRY, JAPANESE BIOCHEMICAL SOCIETY, TOKYO, JP, (1994), vol. 298, ISSN 0021-924X, pages 719 - 725, XP002041430 [X] 17-20 * the whole document *
		[A] - COLLINS F S ET AL, "A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation", GENOME RESEARCH, COLD SPRING HARBOR LABORATORY PRESS, US, (1998), vol. 8, ISSN 1088-9051, pages 1229 - 1231, XP002177106 [A] * the whole document *
		[A] - BOLK S ET AL, "HIGH-THROUGHPUT SNP GENOTYPING USING SINGLE-BASE EXTENSION", AMERICAN JOURNAL OF HUMAN GENETICS, UNIVERSITY OF CHICAGO PRESS, CHICAGO,, US, (1999), vol. 65, no. 4, ISSN 0002-9297, page A97, XP000979094 [A] * the whole document * DOI: http://dx.doi.org/10.1086/302687

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