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Human Genetics, ISSN 0340-6717, 1/2012, Volume 131, Issue 1, pp. 121 - 130
X-chromosome inactivation (XCI) is an essential mechanism in females that compensates for the genome imbalance between females and males. It is known that XCI... 
Human Genetics | Gene Function | Molecular Medicine | Biomedicine | Metabolic Diseases | GENE-ACTION | REPEAT HYPOTHESIS | PATTERN | MOUSE | GENETICS & HEREDITY | X,AUTOSOME TRANSLOCATION | BREAKPOINT | FEMALES | GIRL | AUTOSOME TRANSLOCATIONS | CYTOGENETIC ANALYSIS | Biomarkers - metabolism | Genomic Imprinting | Chromosome Banding | Chromosomes, Human, X - genetics | Oligonucleotide Array Sequence Analysis | Humans | RNA, Messenger - genetics | Child, Preschool | In Situ Hybridization, Fluorescence | Male | Gene Expression Profiling | Chromosomes, Human, Pair 15 - genetics | Reverse Transcriptase Polymerase Chain Reaction | DNA Methylation | Phenotype | Membrane Transport Proteins - genetics | Chromosome Aberrations | Polymorphism, Single Nucleotide - genetics | Prader-Willi Syndrome - genetics | snRNP Core Proteins - genetics | Real-Time Polymerase Chain Reaction | Karyotype | Translocation, Genetic - genetics | X Chromosome Inactivation | Sulfites | Prader-Willi syndrome | Analysis | Genomics | Cytogenetics | Genomes | Genetic aspects | Methylation | Chromosomes | Index Medicus | Breakpoints | Bisulfite | Androgen receptors | Karyotypes | Single-nucleotide polymorphism | Promoters | X-chromosome inactivation | Polymerase chain reaction | Chromosome translocations | DNA microarrays | Fluorescence in situ hybridization | DNA methylation | Replication | chromosome 15 | Ubiquitin-protein ligase
Journal Article
by Tsoi, L.C and Spain, S.L and Knight, J and Ellinghaus, E and Stuart, P.E and Capon, F and Ding, J and Li, J and Tejasvi, T and Gudjonsson, J.E and Kang, H and Allen, M.H and McManus, R and Novelli, G and Samuelsson, L and Schalkwijk, J and Stahle, M and Burden, A.D and Smith, C.H and Cork, M.J and Estivill, X and Bowcock, A and Krueger, G.G and Weger, W and Worthington, J and Tazi-Ahnini, R and Nestle, F.O and Hayday, A and Hoffmann, P and Winkelmann, J and Wijmenga, C and Langford, C and Edkins, S and Anews, R and Blackburn, H and Strange, A and Band, G and Pearson, R and Vukcevic, D and Spencer, C.C and Deloukas, P and Mrowietz, U and Schreiber, S and Weidinger, S and Koks, S and Kingo, K and Esko, T and Metspalu, A and Lim, H.W and Voorhees, J.J and Weichenthal, M and Wichmann, H.E and Chanan, V and Rosen, C.F and Rahman, P and Gladman, D.D and Griffiths, C.E and Reis, A and Kere, J and Duffin, K.C and Helms, C and Goldgar, D and Li, Y and Paschall, J and Malloy, M.J and Pullinger, C.R and Kane, J.P and Gardner, J and Perlmutter, A and Miner, A and Feng, B.J and Hiremagalore, R and Ike, R.W and Christophers, E and Henseler, T and Ruether, A and Schrodi, S.J and Prahalad, S and Guthery, S.L and Hiregalore, R and Donnelly, P and Collaborative Assoc Study Psoriasi and Psoriasis Assoc Genetics Extension and Genetic Anal Psoriasis Consortium and Wellcome Trust Case Control Consor and Psoriasis Association Genetics Extension and Genetic Analysis of Psoriasis Consortium and Collaborative Association Study of Psoriasis (CASP) and Wellcome Trust Case Control Consortium 2 and Sahlgrenska akademin and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 12, pp. 1341 - 1348
To gain further insight into the genetic architecture of psoriasis, we conducted a meta-analysis of 3 genome-wide association studies (GWAS) and 2 independent... 
COMMON VARIANTS | SIGNALING PATHWAYS | MULTIPLE COMMON | INTERFERON-GAMMA | TH17 DIFFERENTIATION | GENETICS & HEREDITY | GENE-EXPRESSION | T-CELL DEVELOPMENT | GENOME-WIDE ASSOCIATION | CELIAC-DISEASE | NEGATIVE REGULATOR | Oligonucleotide Array Sequence Analysis | Humans | Immunity, Innate - genetics | Genetic Loci | CARD Signaling Adaptor Proteins - genetics | Psoriasis - genetics | Core Binding Factor Alpha 3 Subunit - immunology | STAT3 Transcription Factor - genetics | Skin - immunology | Psoriasis - immunology | CARD Signaling Adaptor Proteins - immunology | DEAD Box Protein 58 | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Guanylate Cyclase - immunology | Membrane Proteins - genetics | Membrane Proteins - immunology | GTPase-Activating Proteins - immunology | DEAD-box RNA Helicases - genetics | Core Binding Factor Alpha 3 Subunit - genetics | DEAD-box RNA Helicases - immunology | Guanylate Cyclase - genetics | T-Lymphocytes - immunology | Polymorphism, Single Nucleotide | GTPase-Activating Proteins - genetics | STAT3 Transcription Factor - immunology | Psoriasis | Physiological aspects | Disease susceptibility | Genetic aspects | Research | Autoimmune diseases | Gene expression | Chromosomes | Risk factors | Index Medicus | genetic analysis | innate immunity | Dermatologi och venereologi | Dermatology and Venereal Diseases | psoriasis
Journal Article
09/2013
Ring chromosome 15 is a rare disorder. The mechanism of ring chromosome formation is usually associated with loss of genetic material. Its clinical features... 
Rwandan patient | Chromosome 15 en anneau | retard de croissance | Ring chromosome 15 | growth retardation | patiente Rwandais
Web Resource
Journal Article
Journal Article
The Plant Journal, ISSN 0960-7412, 10/2015, Volume 84, Issue 1, pp. 216 - 227
Barley ( Hordeum vulgare L.) possesses a large and highly repetitive genome of 5.1 Gb that has hindered the development of a complete sequence. In 2012, the... 
Barley | centromere | Hordeum vulgare | BAC | EST | Aegilops tauschii | gene distribution | recombination frequency | sequencing | synteny | Harv | BAC sequencing | Hordeum vulgare L | centromere BACs | HarvEST:Barley | Chromosomes, Artificial, Bacterial - genetics | Molecular Sequence Data | Genome, Plant - genetics | Hordeum - genetics | Bank clearinghouses | Genes | Genomics | Index Medicus | Resource
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2018, Volume 176, Issue 2, pp. 443 - 449
Journal Article