Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid
Reexamination Certificate
2007-12-11
2007-12-11
Whisenant, Ethan (Department: 1634)
Chemistry: molecular biology and microbiology
Measuring or testing process involving enzymes or...
Involving nucleic acid
C536S023100, C536S024200
Reexamination Certificate
active
11119755
ABSTRACT:
The present invention relates to methods for detecting a change in chromosomal structure. These methods employ labeled probes that bind nucleic acids. For example, these probes may be comprised of nucleic acids or nucleic acid analogs and a detectable label.
REFERENCES:
patent: 5527675 (1996-06-01), Coull et al.
patent: 5539082 (1996-07-01), Nielsen et al.
patent: 5623049 (1997-04-01), Lobberding et al.
patent: 5714331 (1998-02-01), Buchardt et al.
patent: 5736336 (1998-04-01), Buchardt et al.
patent: 5750340 (1998-05-01), Kim et al.
patent: 5766855 (1998-06-01), Buchardt et al.
patent: 5773571 (1998-06-01), Nielsen et al.
patent: 5786461 (1998-07-01), Buchardt et al.
patent: 5837459 (1998-11-01), Berg et al.
patent: 5891625 (1999-04-01), Buchardt et al.
patent: 5972610 (1999-10-01), Buchardt et al.
patent: 5986053 (1999-11-01), Ecker et al.
patent: 6025126 (2000-02-01), Westbrook
patent: 6107470 (2000-08-01), Nielsen et al.
patent: 6201103 (2001-03-01), Nielsen et al.
patent: 6228982 (2001-05-01), Norden et al.
patent: 6357163 (2002-03-01), Buchardt et al.
patent: 6414133 (2002-07-01), Dietz-Band et al.
patent: 6730474 (2004-05-01), van Dongen et al.
patent: 2002/0192692 (2002-12-01), Palanisamy et al.
patent: 2003/0096255 (2003-05-01), Felix et al.
patent: WO 96/04000 (1996-02-01), None
patent: WO 97/14026 (1997-04-01), None
patent: WO 98/51817 (1998-11-01), None
patent: WO 02/093130 (2002-11-01), None
Sinclair et al., Improved sensitivity of BCR-ABL detection : A triple -probe three-color fluorescence in situ hybridization system. Blood 90(4) : 1395-1402 (1997).
US 5,714,331 (withdrawn).
U.S. Appl. No. 11/121,086, Poulsen.
Speel,Histochem. Cell Biol., 112: 89-113 (1999).
Rudkin and Stollar,Nature, 265: 472-73 (1977).
Luke and Shepelsky,Cell Vision5: 49-53 (1998).
Szeles,Acta Microbiol., Immunol. Hungarica, 49: 69-80 (2002).
Eils et al.,Cytogenetics Cell Genet.82: 160-71 (1998).
Macville M. et al.,Histochem. Cell. Biol.108: 299-305 (1997).
Tkachuk et al.,Science250: 559-62 (1990).
Henegariu et al.,Lab. Invest., 81: 483-91 (2001).
Schrock et al.,Science, 273: 494-497 (1996).
Fan et al.,Genetic Testing, 4: 9-14 (2000).
Hilgenfeld et al.,British J. Haematol.113: 305-17 (2001).
Liehr et al.,Cytogenet. Genome Res.97: 43-50 (2002).
Anderson et al.,Radiation Research159, 40-48 (2003).
Nederlof et al.,Cytometry11: 126-131 (1990).
Dauwerse et al.,Human Molecular Genetics, vol. 1, No. 8 593-598.
Pellestor et al.,Chromosome Research10: 359-367, (2002).
S. Strehl et al., “The network of fusion genes,”Blood102: 845a-846a Abstract (2003).
M. Van Der Burg et al., “Split-signal FISH for detection of chromosome aberrations in acute lymphoblastic leukemia,”Leukemia, 18 (5): 895-908 (2004).
M. Van Der Burg et al., “Rapid and sensitive detection of all types ofMLLgene translocations with a single FISH probe set,”Leukemia, 13 (12): 2107-2113 (1999).
K. A. Rack et al., “FISH detection of chromosome 14q32/lgH translocations: Evaluation in follicular lymphoma,”British J. Haematol., 103 (2): 495-504 (1998).
Z. Chen et al., “Some Observations on Fluorescence in Situ hybridization Evaluation of Chronic Myelocytic Leukemia,”Cancer Genetics and Cytogenetics98 (1): 1-3 (1997).
M. Koenig et al., “A highly specific and sensitive fluorescence in situ hybridization assay for the detection of t (4;11)(q21;q23) and concurrent submicroscopic deletions in acute leukaemias,”British J. Haematol., 116 (4): 758-764 (2002).
Petersen Kenneth Heesche
Poulsen Susan Medom
Poulsen Tim Svenstrup
Dako Denmark A/S
Finnegan & Henderson et al.
Whisenant Ethan
LandOfFree
Methods for detecting chromosome aberrations does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Methods for detecting chromosome aberrations, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Methods for detecting chromosome aberrations will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3874396