Melvyn I Marquis
Examiner (ID: 16161)
Most Active Art Unit | 1501 |
Art Unit(s) | 1402, 1505, 1503, 1501, 1712, 2200, 1754, 1401 |
Total Applications | 2620 |
Issued Applications | 2300 |
Pending Applications | 26 |
Abandoned Applications | 294 |
Applications
Application number | Title of the application | Filing Date | Status |
---|---|---|---|
Array
(
[id] => 8289761
[patent_doc_number] => 20120178087
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-07-12
[patent_title] => 'Genotyping Assay to Predict Gamma Glutamyl Hydrolase (GGH) Activity'
[patent_app_type] => utility
[patent_app_number] => 13/400394
[patent_app_country] => US
[patent_app_date] => 2012-02-20
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 1
[patent_figures_cnt] => 1
[patent_no_of_words] => 10203
[patent_no_of_claims] => 13
[patent_no_of_ind_claims] => 4
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[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13400394
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/400394 | Genotyping Assay to Predict Gamma Glutamyl Hydrolase (GGH) Activity | Feb 19, 2012 | Abandoned |
Array
(
[id] => 10241377
[patent_doc_number] => 20150126373
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2015-05-07
[patent_title] => 'ULTRA-HIGH SENSITIVE MONITORING OF EARLY TRANSPLANTATION FAILURE'
[patent_app_type] => utility
[patent_app_number] => 14/000485
[patent_app_country] => US
[patent_app_date] => 2012-02-16
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 9
[patent_figures_cnt] => 9
[patent_no_of_words] => 8982
[patent_no_of_claims] => 31
[patent_no_of_ind_claims] => 4
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 14000485
[rel_patent_id] =>[rel_patent_doc_number] =>) 14/000485 | Ultra-high sensitive monitoring of early transplantation failure | Feb 15, 2012 | Issued |
Array
(
[id] => 8382170
[patent_doc_number] => 20120225798
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-09-06
[patent_title] => 'METHOD FOR NON-INVASIVE PRENATAL DIAGNOSIS'
[patent_app_type] => utility
[patent_app_number] => 13/369000
[patent_app_country] => US
[patent_app_date] => 2012-02-08
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 9
[patent_figures_cnt] => 9
[patent_no_of_words] => 13092
[patent_no_of_claims] => 17
[patent_no_of_ind_claims] => 4
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[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13369000
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/369000 | METHOD FOR NON-INVASIVE PRENATAL DIAGNOSIS | Feb 7, 2012 | Abandoned |
Array
(
[id] => 8211695
[patent_doc_number] => 20120129957
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-05-24
[patent_title] => 'ANALYZING THE FMR1 GENE'
[patent_app_type] => utility
[patent_app_number] => 13/360349
[patent_app_country] => US
[patent_app_date] => 2012-01-27
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 24
[patent_figures_cnt] => 24
[patent_no_of_words] => 44224
[patent_no_of_claims] => 13
[patent_no_of_ind_claims] => 3
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[patent_maintenance] => 1
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[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0129/20120129957.pdf
[firstpage_image] =>[orig_patent_app_number] => 13360349
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/360349 | ANALYZING THE FMR1 GENE | Jan 26, 2012 | Abandoned |
Array
(
[id] => 9135612
[patent_doc_number] => 20130296328
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-11-07
[patent_title] => 'EPIGENETIC PORTRAITS OF HUMAN BREAST CANCERS'
[patent_app_type] => utility
[patent_app_number] => 13/980809
[patent_app_country] => US
[patent_app_date] => 2012-01-20
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 33
[patent_figures_cnt] => 33
[patent_no_of_words] => 25693
[patent_no_of_claims] => 26
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[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13980809
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/980809 | EPIGENETIC PORTRAITS OF HUMAN BREAST CANCERS | Jan 19, 2012 | Abandoned |
Array
(
[id] => 9135460
[patent_doc_number] => 20130296175
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-11-07
[patent_title] => 'Genetic Variants as Markers for Use in Urinary Bladder Cancer Risk Assessment, Diagnosis, Prognosis and Treatment'
[patent_app_type] => utility
[patent_app_number] => 13/979119
[patent_app_country] => US
[patent_app_date] => 2012-01-12
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 4
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[patent_no_of_words] => 39391
[patent_no_of_claims] => 70
[patent_no_of_ind_claims] => 32
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[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13979119
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/979119 | Genetic Variants as Markers for Use in Urinary Bladder Cancer Risk Assessment, Diagnosis, Prognosis and Treatment | Jan 11, 2012 | Abandoned |
Array
(
[id] => 9435379
[patent_doc_number] => 20140113286
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2014-04-24
[patent_title] => 'Epigenomic Markers of Cancer Metastasis'
[patent_app_type] => utility
[patent_app_number] => 13/997100
[patent_app_country] => US
[patent_app_date] => 2011-12-21
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 12
[patent_figures_cnt] => 12
[patent_no_of_words] => 11414
[patent_no_of_claims] => 29
[patent_no_of_ind_claims] => 3
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[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13997100
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/997100 | Epigenomic Markers of Cancer Metastasis | Dec 20, 2011 | Abandoned |
Array
(
[id] => 9306506
[patent_doc_number] => 20140045180
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2014-02-13
[patent_title] => 'METHOD FOR DETECTING METHYLATION OF COLORECTAL CANCER SPECIFIC METHYLATION MARKER GENE FOR COLORECTAL CANCER DIAGNOSIS'
[patent_app_type] => utility
[patent_app_number] => 13/994732
[patent_app_country] => US
[patent_app_date] => 2011-12-16
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 4
[patent_figures_cnt] => 4
[patent_no_of_words] => 10769
[patent_no_of_claims] => 16
[patent_no_of_ind_claims] => 4
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[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13994732
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/994732 | Method for detecting methylation of colorectal cancer specific methylation marker gene for colorectal cancer diagnosis | Dec 15, 2011 | Issued |
Array
(
[id] => 9449370
[patent_doc_number] => 20140120540
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2014-05-01
[patent_title] => 'METHODS OF DETECTING GENE FUSIONS'
[patent_app_type] => utility
[patent_app_number] => 14/130397
[patent_app_country] => US
[patent_app_date] => 2011-12-07
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 12
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[patent_no_of_words] => 22285
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[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 14130397
[rel_patent_id] =>[rel_patent_doc_number] =>) 14/130397 | Methods of detecting gene fusions | Dec 6, 2011 | Issued |
Array
(
[id] => 9943932
[patent_doc_number] => 08993232
[patent_country] => US
[patent_kind] => B2
[patent_issue_date] => 2015-03-31
[patent_title] => 'Identification of the causative mutation for leopard complex spotting and congenital stationary night blindness in equines and a method for testing for same'
[patent_app_type] => utility
[patent_app_number] => 13/373911
[patent_app_country] => US
[patent_app_date] => 2011-12-05
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 7
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[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => patent
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13373911
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/373911 | Identification of the causative mutation for leopard complex spotting and congenital stationary night blindness in equines and a method for testing for same | Dec 4, 2011 | Issued |
Array
(
[id] => 8393612
[patent_doc_number] => 20120231452
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-09-13
[patent_title] => 'ASSAY FOR METHYLATION IN THE GST-PI GENE'
[patent_app_type] => utility
[patent_app_number] => 13/307573
[patent_app_country] => US
[patent_app_date] => 2011-11-30
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 20
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[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13307573
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/307573 | ASSAY FOR METHYLATION IN THE GST-PI GENE | Nov 29, 2011 | Abandoned |
Array
(
[id] => 7807532
[patent_doc_number] => 20120058486
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-03-08
[patent_title] => 'GENETIC RISK ASSESSMENT TECHNOLOGY FOR EPITHELIAL CANCER INVOLVING GENE-ENVIRONMENT INTERACTION BETWEEN ERCC5 AND TOBACCO USE'
[patent_app_type] => utility
[patent_app_number] => 13/294360
[patent_app_country] => US
[patent_app_date] => 2011-11-11
[patent_effective_date] => 0000-00-00
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[pdf_file] => publications/A1/0058/20120058486.pdf
[firstpage_image] =>[orig_patent_app_number] => 13294360
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/294360 | GENETIC RISK ASSESSMENT TECHNOLOGY FOR EPITHELIAL CANCER INVOLVING GENE-ENVIRONMENT INTERACTION BETWEEN ERCC5 AND TOBACCO USE | Nov 10, 2011 | Abandoned |
Array
(
[id] => 8811107
[patent_doc_number] => 20130112152
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-05-09
[patent_title] => 'SNP Alleles Associated with Leopard Complex Spotting and Congenital Stationary Blindness and Agents, Methods and Kits Thereof'
[patent_app_type] => utility
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[rel_patent_id] =>[rel_patent_doc_number] =>) 13/292688 | SNP Alleles Associated with Leopard Complex Spotting and Congenital Stationary Blindness and Agents, Methods and Kits Thereof | Nov 8, 2011 | Abandoned |
Array
(
[id] => 11199316
[patent_doc_number] => 09429520
[patent_country] => US
[patent_kind] => B2
[patent_issue_date] => 2016-08-30
[patent_title] => 'Enrichment and identification of fetal cells in maternal blood and ligands for such use'
[patent_app_type] => utility
[patent_app_number] => 13/883455
[patent_app_country] => US
[patent_app_date] => 2011-11-09
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[rel_patent_id] =>[rel_patent_doc_number] =>) 13/883455 | Enrichment and identification of fetal cells in maternal blood and ligands for such use | Nov 8, 2011 | Issued |
Array
(
[id] => 8198067
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[patent_kind] => A1
[patent_issue_date] => 2012-05-17
[patent_title] => 'METHODS AND KITS FOR MULTIPLEX AMPLIFICATION OF SHORT TANDEM REPEAT LOCI'
[patent_app_type] => utility
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[rel_patent_id] =>[rel_patent_doc_number] =>) 13/291976 | METHODS AND KITS FOR MULTIPLEX AMPLIFICATION OF SHORT TANDEM REPEAT LOCI | Nov 7, 2011 | Abandoned |
Array
(
[id] => 9004318
[patent_doc_number] => 20130225443
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-08-29
[patent_title] => 'METHOD OF EXAMINING POLYCYSTIC KIDNEY DISEASE AND METHOD OF SCREENING FOR THERAPEUTIC AGENT OF THE DISEASE'
[patent_app_type] => utility
[patent_app_number] => 13/883735
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Array
(
[id] => 8094755
[patent_doc_number] => 20120082982
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2012-04-05
[patent_title] => 'CYSTIC FIBROSIS GENE MUTATIONS'
[patent_app_type] => utility
[patent_app_number] => 13/290814
[patent_app_country] => US
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[firstpage_image] =>[orig_patent_app_number] => 13290814
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/290814 | Cystic fibrosis gene mutations | Nov 6, 2011 | Issued |
Array
(
[id] => 9121996
[patent_doc_number] => 20130288918
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[patent_kind] => A1
[patent_issue_date] => 2013-10-31
[patent_title] => 'Colorectal Cancer Screening Method'
[patent_app_type] => utility
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[patent_app_country] => US
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Array
(
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[patent_title] => 'GENETIC POLYMORPHISMS ASSOCIATED WITH LIVER FIBROSIS METHODS OF DETECTION AND USES THEREOF'
[patent_app_type] => utility
[patent_app_number] => 13/283344
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Array
(
[id] => 9081907
[patent_doc_number] => 20130267437
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2013-10-10
[patent_title] => 'USE OF SPECIFIC GENES OR THEIR ENCODED PROTEINS FOR A PROGNOSIS METHOD OF CLASSIFIED LUNG CANCER'
[patent_app_type] => utility
[patent_app_number] => 13/880419
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[rel_patent_id] =>[rel_patent_doc_number] =>) 13/880419 | USE OF SPECIFIC GENES OR THEIR ENCODED PROTEINS FOR A PROGNOSIS METHOD OF CLASSIFIED LUNG CANCER | Oct 19, 2011 | Abandoned |