Chromosome Mapping Concept

subject area of

• 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread  Journal Articles
• Molecular characterization of the Pseudomonas aeruginosa serotype O5 (PAO1) B‐band lipopolysaccharide gene cluster  Journal Articles
• sli-3 Negatively Regulates the LET-23/Epidermal Growth Factor Receptor-Mediated Vulval Induction Pathway in Caenorhabditis elegans  Journal Articles
• A Novel CpG Island Set Identifies Tissue-Specific Methylation at Developmental Gene Loci  Journal Articles
• A Reanalysis of Protein Polymorphism in Drosophila Melanogaster, D. Simulans, D. Sechellia and D. Mauritiana: Effects of Population Size and Selection  Journal Articles
• A TaqI RFLP In Xq26-Xqter detected by pX45h [HGMB no. DXS100h]  Journal Articles
• A TaqI RFLP in Xq26–qter detected by pX301b [DXS311]  Journal Articles
• A comprehensive study of genic variation in natural populations of Drosophila melanogaster. VI. Patterns and processes of genic divergence between D. melanogaster and its sibling species, Drosophila simulans.  Journal Articles
• A gene family inDrosophila melanogastercoding for trypsin-like enzymes  Journal Articles
• A genome-wide association study of sporadic ALS in a homogenous Irish population  Journal Articles
• A genome-wide linkage and association scan reveals novel loci for autism  Journal Articles
• A novel candidate region for ALS on chromosome 14q11.2  Journal Articles
• A phosphate transport system is required for symbiotic nitrogen fixation by Rhizobium meliloti  Journal Articles
• A toolkit for rapid gene mapping in the nematode Caenorhabditis briggsae  Journal Articles
• A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity  Journal Articles
• Adenovirus-2 Messengers--An Example of Baroque Molecular Architecture  Journal Articles
• Advancing Biomarker Discovery and Therapeutic Targets in Duchenne Muscular Dystrophy: A Comprehensive Review.  Journal Articles
• Affected members of melanoma‐prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF  Journal Articles
• An msbB Homologue Carried in Plasmid pO157 Encodes an Acyltransferase Involved in Lipid A Biosynthesis in Escherichia coli O157:H7  Journal Articles
• An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.  Journal Articles
• Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD  Journal Articles
• Analysis of a 1600-kilobase Rhizobium meliloti megaplasmid using defined deletions generated in vivo.  Journal Articles
• Anomalous Migration of PCR Products Using Nondenaturing Polyacrylamide Gel Electrophoresis: The Amelogenin Sex-Typing System  Journal Articles
• Are entrenched characters developmentally constrained? Creating biramous limbs in an insect  Journal Articles
• Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2.  Journal Articles
• Assignment of bovine trophinin (TRO) to the q arm of the X chromosome by fluorescence in situ hybridization  Journal Articles
• Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage  Journal Articles
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index  Journal Articles
• Autism and the X chromosome: No linkage to microsatellite loci detected using the affected sibling pair method  Journal Articles
• Breakpoint localization of the marker chromosome associated with the cat eye syndrome.  Journal Articles
• Caenorhabditis briggsae Recombinant Inbred Line Genotypes Reveal Inter-Strain Incompatibility and the Evolution of Recombination  Journal Articles
• Cell death attenuation by `Usurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex  Journal Articles
• Centromeric linkage.  Journal Articles
• Characterization of a lymphoblastoid line deleted for lambda immunoglobulin genes  Journal Articles
• Chromosome-specific alpha satellite DNA from human chromosome 1: Hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA  Journal Articles
• Chromosome-specific alpha satellite DNA: Isolation and mapping of a polymorphic alphoid repeat from human chromosome 10  Journal Articles
• Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.  Journal Articles
• Cloning and 5′ End Nucleotide Sequences of Two Juvenile Hormone-Inducible Vitellogenin Genes of the African Migratory Locust  Journal Articles
• Cloning of a Chromosomal Region Responsible for Streptolysin S Production in Streptococcus pyogenes  Conferences
• Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity  Journal Articles
• Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis  Journal Articles
• Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 ( dip2 ), and its murine homolog  Journal Articles
• Comparative analysis of function and interaction of transcription factors in nematodes: Extensive conservation of orthology coupled to rapid sequence evolution  Journal Articles
• Comparative chromosome painting of pronghorn (Antilocapra americana) and saola (Pseudoryx nghetinhensis) karyotypes with human and dromedary camel probes  Journal Articles
• Comparison of the mutagenic responses of 12 anticancer drugs at the hypoxanthine‐guanine phosphoribosyl transferase and adenosine kinase loci in chinese hamster ovary cells  Journal Articles
• Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements  Journal Articles
• Contribution of SHANK3 Mutations to Autism Spectrum Disorder  Journal Articles
• Contribution of SHANK3 mutations to autism spectrum disorder.  Journal Articles
• Cytogenetic comparison of saola <i>(Pseudoryx nghetinhensis)</i> and cattle <i>(Bos taurus)</i> using G- and Q-banding and FISH  Journal Articles
• DNA Marker Studies Show That Machado Joseph Disease is Not an Allele of The Huntingdon Disease Locus  Journal Articles
• DNA amplification and tumorigenicity of the human melanoma cell line MeWo.  Journal Articles
• Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.  Journal Articles
• Development and Characterization of a Genetic Linkage Map of Cryptococcus neoformans var. neoformans Using Amplified Fragment Length Polymorphisms and Other Markers  Journal Articles
• Developmental T cell receptor gene rearrangements: Relatedness of the α/β and γ/δ T cell precursor  Journal Articles
• DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.  Journal Articles
• Differences Between the Pattern of Developmental Abnormalities in Autism Associated With Duplications 15q11.2-q13 and Idiopathic Autism  Journal Articles
• EFFECTS OF SOME IMMUNOSUPPRESSIVE PROCEDURES ON MYASTHENIA GRAVIS*  Journal Articles
• Effects of misclassification on estimates of relative risk in family history studies  Journal Articles
• Embryonic ζ-Globin Chains in Adults: a Marker for α-Thalassemia-1 Haplotype Due to a >17.5-kb Deletion  Journal Articles
• Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein  Journal Articles
• Evidence for a link between local and seasonal cycles in gene frequencies and latitudinal gene clines in a cyclic parthenogen  Journal Articles
• Evidence for functional hemizygosity at the Emtr locus in CHO cells through segregation analysis  Journal Articles
• Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels  Journal Articles
• Further localization of X-linked hydrocephalus in the chromosomal region Xq28.  Journal Articles
• Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17  Journal Articles
• Generation of a new adenovirus type 12-inducible fragile site by insertion of an artificial U2 locus in the human genome.  Journal Articles
• Genes controlling malathion resistance in a laboratory-selected population of Drosophila melanogaster  Journal Articles
• Genetic Analyses of a Hybrid Cross Between Serotypes A and D Strains of the Human Pathogenic Fungus Cryptococcus neoformans  Journal Articles
• Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Density Lipoprotein Cholesterol  Journal Articles
• Genetic Analysis of Mutations Affecting pckA Regulation in Rhizobium (Sinorhizobium) meliloti  Journal Articles
• Genetic Control of Vulval Development inCaenorhabditis briggsae  Journal Articles
• Genetic and biochemical characterization of an operon involved in the biosynthesis of 3-deoxy-d-manno-octulosonic acid inPseudomonas aeruginosa  Journal Articles
• Genetic and physical analyses of group E exo- mutants of Rhizobium meliloti  Journal Articles
• Genetic map of Rhizobium meliloti megaplasmid pRmeSU47b  Journal Articles
• Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.  Journal Articles
• Genome evolution and speciation genetics of clawed frogs (Xenopus and Silurana)  Journal Articles
• Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias  Journal Articles
• Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors  Journal Articles
• Genome-wide association studies identify loci associated with age at menarche and age at natural menopause  Journal Articles
• Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets  Journal Articles
• Genome-wide meta-analyses identify multiple loci associated with smoking behavior  Journal Articles
• Genomic Dynamics of Transposable Elements in the Western Clawed Frog (Silurana tropicalis)  Journal Articles
• Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations  Journal Articles
• Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the   locus control region  Journal Articles
• Hb S/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype  Journal Articles
• High hemoglobin A2 beta-thalassemia.  Journal Articles
• High-Throughput GoMiner, an 'industrial-strength' integrative gene ontology tool for interpretation of multiple-microarray experiments, with application to studies of Common Variable Immune Deficiency (CVID)  Journal Articles
• Human Chromosome 7: DNA Sequence and Biology  Journal Articles
• Human ERMAP: An Erythroid Adhesion/Receptor Transmembrane Protein  Journal Articles
• Identification of QTLs Associated with Virulence Related Traits and Drug Resistance in Cryptococcus neoformans  Journal Articles
• Identification of an extensive ζ‐α globin gene deletion in a Chinese individual  Journal Articles
• Increased pyruvate orthophosphate dikinase activity results in an alternative gluconeogenic pathway in Rhizobium (Sinorhizobium) meliloti  Journal Articles
• Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome  Journal Articles
• Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome  Journal Articles
• Investigation of Intercellular Salicylic Acid Accumulation during Compatible and Incompatible Arabidopsis-Pseudomonas syringae Interactions Using a Fast Neutron-Generated Mutant Allele of EDS5 Identified by Genetic Mapping and Whole-Genome Sequencing  Journal Articles
• Isolation and Mapping of 45 NotI Linking Clones to Chromosome 22  Journal Articles
• Isolation and characterization of respiratory-deficient mutants of Escherichia coli K-12  Journal Articles
• Isolation and mapping of a polymorphic DNA sequence, DXS312, to Xq27–Xq28  Journal Articles
• Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation  Journal Articles
• Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes  Journal Articles
• Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome  Journal Articles
• Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders  Journal Articles
• Linkage analysis of 26 Canadian breast and breast-ovarian cancer families  Journal Articles
• Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.  Journal Articles
• Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against synteny  Journal Articles
• Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37  Journal Articles
• Localization and linkage of three polymorphic DNA sequences on human chromosome 20  Journal Articles
• Localization of X-Linked Dominant Charcot-Marie-Tooth Disease (CMT 2) to Xq13  Journal Articles
• Loci influencing blood pressure identified using a cardiovascular gene-centric array  Journal Articles
• Low‐depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution  Journal Articles
• Mapping and Regulation of Genes within Salmonella Pathogenicity Island 12 That Contribute to In Vivo Fitness of Salmonella enterica Serovar Typhimurium  Journal Articles
• Mapping autism risk loci using genetic linkage and chromosomal rearrangements  Journal Articles
• Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1→q13.2  Journal Articles
• Mapping of the metalloproteinase gene matrilysin (MMP7) to human chromosome 11q21→q22  Journal Articles
• Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution  Journal Articles
• Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results  Journal Articles
• Molecular Analysis of Phyllodes Tumors Reveals Distinct Changes in the Epithelial and Stromal Components  Journal Articles
• Molecular Genetic Analysis of the Idd4 Locus Implicates the IFN Response in Type 1 Diabetes Susceptibility in Nonobese Diabetic Mice  Journal Articles
• Molecular Polymorphism and Divergence of Duplicated Genes in Tetraploid African Clawed Frogs <b><i>(Xenopus)</i></b>  Journal Articles
• Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients  Journal Articles
• Multiple loci associated with indices of renal function and chronic kidney disease  Journal Articles
• Multiple subelements within the polyomavirus enhancer function synergistically to activate DNA replication.  Journal Articles
• Murine Hn1 on Chromosome 11 is expressed in hemopoietic and brain tissues  Journal Articles
• Mutant Alleles at the Locus elav in Drosophila melanogaster lead to Nervous System Defects. A Developmental-Genetic Analysis  Journal Articles
• Mutants of Rhizobium meliloti defective in succinate metabolism  Journal Articles
• Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy  Journal Articles
• Mutation screening of a neutral amino acid transporter, ASCT1, and its potential role in schizophrenia  Journal Articles
• Mutations in the genestand still disrupt germ cell differentiation inDrosophila ovaries  Journal Articles
• Negative regulation of sigma 54-dependent dctA expression by the transcriptional activator DctD  Journal Articles
• Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes  Journal Articles
• Oral‐facial‐digital syndrome VII is oral‐facial‐digital syndrome I: A clarification  Journal Articles
• Organization and genomic distribution of ?82H? alpha satellite DNA  Journal Articles
• PedSplit: pedigree management for stratified analysis  Journal Articles
• Physical Mapping of 30 CA Repeats on Human Chromosome 22  Journal Articles
• Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.  Journal Articles
• Predictive genetic testing for coronary artery disease  Journal Articles
• Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia  Journal Articles
• Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere‐FRA(X)‐DXS15‐DXS52‐F8C‐telomere  Journal Articles
• Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity  Journal Articles
• Regional localization of 18 human X-linked DNA sequences  Journal Articles
• Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38)  Journal Articles
• Relapse of Wilms' Tumor 13 Years After Original Diagnosis  Journal Articles
• Replication of an Egfr-Wing Shape Association in a Wild-Caught Cohort of Drosophila melanogaster  Journal Articles
• SHRiMP2: Sensitive yet Practical Short Read Mapping  Journal Articles
• Second site mutations specifically suppress the Fix- phenotype of Rhizobium meliloti ndvF mutations on alfalfa: identification of a conditional ndvF-dependent mucoid colony phenotype.  Journal Articles
• Severity of β‐thalassemia due to genotypes involving the IVS‐I‐6 (T→C) mutation  Journal Articles
• Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2  Journal Articles
• Stable transfer of a mouse dihydrofolate reductase gene into a deficient cell line using human adenovirus vector  Journal Articles
• Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22.  Journal Articles
• Structure and Functional Relationships in Human pur H  Journal Articles
• Studies on In Vitro Transformation by DNA and DNA Fragments of Human Adenoviruses and Simian Virus 40  Journal Articles
• Studies on the Transfer RNA Genes of Drosophila  Journal Articles
• Synergism between aphidicolin and adenoviruses in the induction of breaks at fragile sites on human chromosomes  Journal Articles
• Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution  Journal Articles
• Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling  Journal Articles
• The bldD Gene of Streptomyces coelicolor A3(2): a Regulatory Gene Involved in Morphogenesis and Antibiotic Production  Journal Articles
• The DY genes of the cattle MHC: expression and comparative analysis of an unusual class II MHC gene pair  Journal Articles
• The Gene Encoding p120cas, a Novel Catenin, Localizes on Human Chromosome 11q11 (CTNND) and Mouse Chromosome 2 (Catns)  Journal Articles
• The Idd4 Locus Displays Sex-Specific Epistatic Effects on Type 1 Diabetes Susceptibility in Nonobese Diabetic Mice  Journal Articles
• The Intrauterine Diagnosis of Hemoglobin Disorders  Journal Articles
• The Localization of Transfer RNA ₅ ^Lys Genes in Drosophila melanogaster  Journal Articles
• The Transcriptionally Competent U2 Gene Is Necessary and Sufficient for Adenovirus Type 12 Induction of the Fragile Site at 17q21-22  Journal Articles
• The association between malathion resistance and acetylcholinesterase in Drosophila melanogaster  Journal Articles
• The fragile‐X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs)  Journal Articles
• The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation.  Journal Articles
• The proto-oncogene C-KIT maps to canid B-chromosomes  Journal Articles
• Transcriptional upregulation of p21/WAF/Cip1 in myeloid leukemic blasts expressing AML1-ETO  Journal Articles
• Trinucleotide repeats at the FRAXF locus: Frequency and distribution in the general population  Journal Articles
• Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments]  Journal Articles
• Ultraviolet transcriptional unit mapping for the late genes in adenovirus type 2  Journal Articles
• hEST2, the Putative Human Telomerase Catalytic Subunit Gene, Is Up-Regulated in Tumor Cells and during Immortalization  Journal Articles
• ndvF, a novel locus located on megaplasmid pRmeSU47b (pEXO) of Rhizobium meliloti, is required for normal nodule development  Journal Articles
• ‘Putting our heads together’: insights into genomic conservation between human and canine intracranial tumors  Journal Articles