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Extract from the Register of European Patents

EP About this file: EP2009112

EP2009112 - Screening-method for polymorphic markers in HtrA1 gene in neurodegenerative disorders [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  27.11.2009
Database last updated on 19.10.2024
Most recent event   Tooltip27.11.2009Application deemed to be withdrawnpublished on 30.12.2009  [2009/53]
Applicant(s)For all designated states
Universität Duisburg-Essen
Universitätsstrasse 2
45141 Essen / DE
[2009/01]
Inventor(s)01 / Ehrmann, Michael, Prof.
Waldeck 5
45133 Essen / DE
02 / Egensperger, Rupert
Ankelbachweg 8
83727 Schliersee / DE
 [2009/01]
Representative(s)Roth, Carla, et al
König-Szynka-Tilmann-von Renesse
Patentanwälte Partnerschaft mbB
Postfach 11 09 46
40509 Düsseldorf / DE
[N/P]
Former [2009/01]Schönbohm, Carla, et al
König Szynka Tilmann von Renesse Patentanwälte Partnerschaft Lohengrinstrasse 11
40549 Düsseldorf / DE
Application number, filing date07012418.525.06.2007
[2009/01]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report 
No.:EP2009112
Date:31.12.2008
Language:EN
[2009/01]
Search report(s)(Supplementary) European search report - dispatched on:EP21.12.2007
ClassificationIPC:C12Q1/68
[2009/01]
CPC:
C12Q1/6883 (EP); C12Q2600/118 (EP); C12Q2600/156 (EP);
C12Q2600/158 (EP)
Designated contracting states(deleted) [2009/36]
Former [2009/01]AT,  BE,  BG,  CH,  CY,  CZ,  DE,  DK,  EE,  ES,  FI,  FR,  GB,  GR,  HU,  IE,  IS,  IT,  LI,  LT,  LU,  LV,  MC,  MT,  NL,  PL,  PT,  RO,  SE,  SI,  SK,  TR 
TitleGerman:Screening-Verfahren für polymorphe Marker im HtrA1 Gen in Neurodegenerativen Krankheiten[2009/01]
English:Screening-method for polymorphic markers in HtrA1 gene in neurodegenerative disorders[2009/01]
French:Procédé de criblage des marqueurs polymorphiques des maladies neurodègènèratives[2009/01]
Examination procedure01.07.2009Application deemed to be withdrawn, date of legal effect  [2009/53]
12.08.2009Despatch of communication that the application is deemed to be withdrawn, reason: examination fee not paid in time  [2009/53]
Fees paidRenewal fee
20.06.2009Renewal fee patent year 03
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Documents cited:Search[XAY]EP0828003  (SMITHKLINE BEECHAM PLC [GB], et al) [X] 1,4,5,9,11-16,18-23 * the whole document * * D87258; SEQ ID NO: 17 and SEQ ID NO: 18. * * page 3, line 58 - page 4, line 35 * * page 8, lines 10-58 * * page 10, line 35 - page 11, line 36 * * claims 19,20,23,24 * [A] 3,6-8,17 [Y] 2,10;
 [Y]WO2004108899  (US GOV HEALTH & HUMAN SERV [US], et al) [Y] 1-23 * the whole document * * SEQ ID NO: 717 (PRSS11). * * paragraphs [0061] , [0062] , [0126] , [0129] * * page 109 * * claims 1-5 *;
 [Y]US2005164933  (TYMIANSKI MICHAEL [CA], et al) [Y] 1-23 * the whole document * * paragraphs [0007] - [0009] - [0013] , [0048] , [0189] * * table 6 *;
 [YA]  - YANG ZHENGLIN ET AL, "A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.", SCIENCE (NEW YORK, N.Y.) 10 NOV 2006, (20061110), vol. 314, no. 5801, ISSN 1095-9203, pages 992 - 993, XP002460077 [Y] 4-8,14-17 * the whole document * * Supporting online material. * [A] 1-3,9-13,18-23

DOI:   http://dx.doi.org/10.1126/science.1133811
 [YA]  - CORDER E H ET AL, "GENE DOSE OF APOLIPOPROTEIN E TYPE 4 ALLELE AND THE RISK OF ALZHEIMER'S DISEASE IN LATE ONSET FAMILIES", SCIENCE, AMERICAN ASSOCIATION FOR THE ADVANCEMENT OF SCIENCE,, US, (19930813), vol. 261, ISSN 0036-8075, pages 921 - 923, XP000619582 [Y] 9,10 * the whole document * [A] 1-8,11-23

DOI:   http://dx.doi.org/10.1126/science.8346443
 [A]  - OZTURK A ET AL, "Three SNPs in the GSTO1, GSTO2 and PRSS11 genes on chromosome 10 are not associated with age-at-onset of Alzheimer's disease", NEUROBIOLOGY OF AGING, TARRYTOWN, NY, US, (200508), vol. 26, no. 8, ISSN 0197-4580, pages 1161 - 1165, XP004904944 [A] 1-23 * the whole document *

DOI:   http://dx.doi.org/10.1016/j.neurobiolaging.2004.11.001
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