Patent application number | Description | Published |
20110313678 | PROBES AND METHODS FOR DETERMINING THE PRESENCE OR ABSENCE OF GENETIC SEGMENTS - A method for determining the presence or absence of a genetic segment of interest, such as an exon, an intron or a promoter, in a DNA-containing sample, and probe sets for use in such methods, including probe sets comprising oligonucleotide probes having nucleotides sequences selected from those of SEQ ID NOS: 1-101. | 12-22-2011 |
20120065096 | GENOTYPING TOOL FOR IMPROVING THE PROGNOSTIC AND CLINICAL MANAGEMENT OF MS PATIENTS - The invention relates to methods of evaluating MS severity based on analysis of single nucleotide polymorphisms (SNPs) and to products and kits for use in such methods. The methods include a method of assessing a multiple sclerosis disease severity phenotype in a human subject having multiple sclerosis, by determining the genotype of the subject at one or more positions of single nucleotide polymorphism (SNP) selected from: rs | 03-15-2012 |
20120172239 | METHOD FOR THE IDENTIFICATION BY MOLECULAR TECHNIQUES OF GENETIC VARIANTS THAT ENCODE NO D ANTIGEN (D-) AND ALTERED C ANTIGEN (C+W) - The invention relates to genotyping and blood cell antigen determination. In particular, the invention addresses discriminating the RHD*DIIIa-CE(4-7)-D or RHD*DIIIa-CE(4-7)-D)-like blood type variants, from RHD*DIIIa, RHD*DIVa-2 and other blood type variants. The invention provides methods for genotyping a subject, comprising:
| 07-05-2012 |
20120215459 | HIGH THROUGHPUT DETECTION OF GENOMIC COPY NUMBER VARIATIONS - The invention relates to methods and algorithms for detecting and analysis of copy number variances in a genetic segment. The invention also relates to a computer implemented sequential method of processing and interpreting experimental data generated by genotyping nucleic acid-chips or nucleic acid-beads based on detection of a hybridization signal. | 08-23-2012 |
20130263294 | MARKERS FOR JOINT DISPLASIA, OSTEOARTHRITIS AND CONDITIONS SECONDARY THERETO - A method for predicting risk of joint dysplasia, osteoarthritis and/or a condition that is secondary to joint dysplasia in a mammalian subject of the order Carnivora, the method comprising: (a) determining the genotype of said subject in respect of one or more genetic polymorphisms and/or alterations, such as polymorphisms in the CHST3 gene; and (b) providing a prediction of said risk based on said genotype. Products for use in such a method and related methods of determining propensity of a subject to respond to therapy and of selective breeding, are also disclosed. | 10-03-2013 |
20140220567 | DISCRIMINATION OF BLOOD TYPE VARIANTS - The present invention provides a method for detecting the presence or absence of, or for discriminating between, blood type variants, including RHD*r′s, RHD*DIIIa, RHD*DIVa-2, RHCE*cs | 08-07-2014 |
20140255923 | DISCRIMINATION OF BLOOD TYPE VARIANTS - The present invention provides a method for detecting the presence or absence of, or for discriminating between, blood type variants, including RHD*r′s, RHD*DIIIa and RHD*DIVa-2. The method comprises amplifying by PCR a sample obtained from a human subject at intron 3 of the RHD gene locus. The invention also provides products, in particular, probes, primers and kits for use in the method of the invention. | 09-11-2014 |
20150376708 | PROBES AND METHODS FOR DETERMINING THE PRESENCE OR ABSENCE OF GENETIC SEGMENTS - A method for determining the presence or absence of a genetic segment of interest, such as an exon, an intron or a promoter, in a DNA-containing sample, and probe sets for use in such methods, including probe sets comprising oligonucleotide probes having nucleotides sequences selected from those of SEQ ID NOS: 1-101. | 12-31-2015 |
20160032386 | GENETIC MARKERS FOR OSTEOARTHRITIS - A method for predicting the severity or progression of OA in a human subject, comprising: determining the identity of at least one allele at each of at least 4 positions of single nucleotide polymorphism (SNPs) selected from the group consisting of: rs2206593, rs10465850, rs780094, rs1374281, rs1143634, rs2073508, rs2243250, rs4720262, rs917760, rs7838918, rs12009, rs730720, rs874692, rs893953, rs1799750, rs10845493, rs11054704, rs7986347, rs1802536, rs10519263, rs7342880, rs16947882 and rs10413815, and one or more SNPs in linkage disequilibrium at a level of at least R | 02-04-2016 |
20160060696 | METHOD FOR THE IDENTIFICATION BY MOLECULAR TECHNIQUES OF GENETIC VARIANTS THAT ENCODE NO D ANTIGEN (D-) AND ALTERED C ANTIGEN (C+W) - The invention relates to genotyping and blood cell antigen determination. In particular, the invention addresses discriminating the RHD*DIIIa-CE(4-7)-D or RHD*DIIIa-CE(4-7)-D)-like blood type variants, from RHD*DIIIa, RHD*DIVa-2 and other blood type variants. The invention provides methods for genotyping a subject, comprising determining at least 4 markers in a sample that has been obtained from the subject, wherein the markers comprise:
| 03-03-2016 |
Patent application number | Description | Published |
20120202487 | Signaling for Legacy Terminal Operation in Harmonized Bands - Network nodes and methods therein for enabling use, in a cell, of different types of mobile terminals. A method in a network node ( | 08-09-2012 |
20140044023 | Methods and Network Nodes in a Telecommunication System - A method in a user equipment ( | 02-13-2014 |
20140066057 | Method and Network Nodes in a Telecommunication System - A method in a user equipment ( | 03-06-2014 |
20140140290 | Release-Independent Modifications of Network Parameters | 05-22-2014 |
20150098425 | SECONDARY CELLS IN OVERLAPPING BANDS - Systems and methods relating to configuring a Secondary Component Carrier (SCC) for a wireless device in a cellular communications network are disclosed. In some embodiments, the method comprises obtaining capabilities of the wireless device, where the capabilities indicate a frequency band combination supported by the wireless device. The frequency band combination supported by the wireless device includes a first frequency band supported by a base station and the wireless device used for a Primary Cell (PCell) of the wireless device and a second frequency band supported by the wireless device but not supported by the base station. The method further comprises identifying an overlap between the second frequency band supported by the wireless device but not supported by the base station and a third frequency band supported by the base station but not supported by the wireless device and configuring the SCC for the wireless device in the overlap. | 04-09-2015 |
20150111608 | Methods and Apparatus for Adjusting Maximum Output Power Level - The present invention relates to a method implemented by a wireless device in a wireless communication system, for adjusting a maximum output power level of the wireless device. The method comprises obtaining ( | 04-23-2015 |
20150148052 | Signaling for Legacy Terminal Operation in Harmonized Bands - Network nodes and methods therein for enabling use, in a cell, of different types of mobile terminals. A method in a network node ( | 05-28-2015 |
Patent application number | Description | Published |
20140015290 | Airplane Seat Provided with a Reinforcing Strip for Absorbing Impacts - The seat according to the invention makes it possible to absorb, in the event of a frontal impact of an airplane, the rocking to which a passenger in a seat located behind the seat according to the invention is subjected. | 01-16-2014 |
20150367943 | VEHICLE SEAT COMPRISING AN AREA THAT IS DEFORMABLE IN THE EVENT OF AN IMPACT - A vehicle seat for a passenger, comprising a backrest having a front face directed towards the passenger and a rear face opposite the front face, and a seat part having an upper face directed towards the passenger and a lower face opposite the upper face, wherein the rear face of the backrest and/or the lower face of the seat part comprise(s) at least one area that is deformable in the event of an impact, towards the front face of the backrest and/or towards the upper face of the seat part respectively, and in that the front face and rear face of the backrest, and/or the upper face and lower face of the seat part are located at a distance from each other, at least at said at least one deformable area, so as to define a clearance space, said at least one deformable area of the rear face of the backrest and/or of the lower face of the seat part being configured so as to deform into the clearance space in the event of an impact on the rear face of the backrest and/or the lower face of the seat part, without transmitting the impact to the front face of the backrest and/or the upper face of the seat part respectively. | 12-24-2015 |
20160046224 | VEHICLE SEAT EQUIPPED WITH A FOLD-DOWN ELEMENT, SUCH AS A TRAY - The transport vehicle seat allows to avoid the violent collision of a passenger's head located on the seat placed behind and to dampen the violent forward rocking of this passenger, in case of a frontal collision of the transport vehicle. The seat includes a pivotably mounted fold-down element ( | 02-18-2016 |