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One or more keywords matched the following items that are connected to Kwiatkowski, David
Item TypeName
Academic Article Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.
Academic Article Fine mapping of the nail-patella syndrome locus at 9q34.
Academic Article Dinucleotide repeat polymorphism at the D9S119 locus (9q22-34).
Academic Article Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse.
Academic Article Genomic organization and chromosomal location of murine Cdc42.
Academic Article Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease.
Academic Article Chromosome 12q harbors multiple genetic loci related to asthma and asthma-related phenotypes.
Academic Article Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.
Academic Article Dinucleotide repeat polymorphism at the D9S120 locus (9q31-34).
Academic Article Dinucleotide repeat polymorphism at the GSN locus (9q32-34).
Academic Article Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.
Academic Article Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndrome.
Academic Article The spontaneous coat color mutant white nose (wn) maps to murine chromosome 15.
Academic Article Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.
Academic Article Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996.
Academic Article Dinucleotide repeat polymorphism at the D9S112 locus (9q31-34).
Academic Article Dinucleotide repeat polymorphism at the D9S116 locus (9q31-34).
Academic Article Construction of a GT polymorphism map of human 9q.
Academic Article The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD).
Academic Article Dinucleotide repeat polymorphism at the D9S121 locus (9q31-34).
Academic Article The gelsolin (GSN) cDNA clone, from 9q32-34, identifies BclI and StuI RFLPs.
Academic Article Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.
Academic Article Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.
Academic Article Dinucleotide repeat polymorphism at the ABL locus (9q34).
Academic Article Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.
Academic Article Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes.
Academic Article Regional localization of 64 cosmid contigs, including 18 genes and 14 markers, to intervals on human chromosome 9q34.
Academic Article Three dinucleotide repeat polymorphisms on chromosome 9 (D9S200, D9S201, D9S199).
Academic Article Dinucleotide repeat polymorphism at the IFNA locus (9p22).
Academic Article Cloning and chromosomal localization of the human cytoskeletal alpha-actinin gene reveals linkage to the beta-spectrin gene.
Academic Article Dinucleotide repeat polymorphism at the D9S115 locus (9q31-34).
Academic Article Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1.
Academic Article Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.
Academic Article Dinucleotide repeat polymorphism at the D9S118 locus (9q31-34).
Academic Article Human complement factor I: analysis of cDNA-derived primary structure and assignment of its gene to chromosome 4.
Academic Article A 5.4-Mb continuous pulsed-field gel electrophoresis map of human 9q34.1 between ABL and D9S114, including the tuberous sclerosis (TSC1) region.
Academic Article Report and abstracts of the Second International Workshop on Human Chromosome 9 Mapping 1993.
Academic Article Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1.
Academic Article Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.
Academic Article Identification of critical functional and regulatory domains in gelsolin.
Academic Article Cosmid contigs from the tuberous sclerosis candidate region on chromosome 9q34.
Academic Article A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference.
Academic Article Human gene for torsion dystonia located on chromosome 9q32-q34.
Academic Article Human XPMC2H: cDNA cloning, mapping to 9q34, genomic structure, and evaluation as TSC1.
Academic Article A genetic linkage map of human chromosome 9q.
Academic Article Report and abstracts of the First International Workshop on Chromosome 9. Held at Girton College Cambridge, UK, 22-24 March, 1992.
Academic Article Dinucleotide repeat polymorphism at the D9S117 locus (9q31-34).
Academic Article Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
Academic Article COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type II.
Academic Article Potential location of a bladder tumor suppressor gene on chromosome 9q at 9q13 to 9q22.1.
Academic Article Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations.
Academic Article IL10 gene polymorphisms are associated with asthma phenotypes in children.
Academic Article An index marker map of chromosome 9 provides strong evidence for positive interference.
Academic Article Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1).
Academic Article Localization of gelsolin proximal to ABL on chromosome 9.
Academic Article Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
Academic Article Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomas.
Academic Article A high-resolution linkage map of human 9q34.1.
Academic Article Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28.
Academic Article A radiation-reduced hybrid cell line containing 5 Mb/17 cM of human DNA from 9q34.
Academic Article Tuberous sclerosis.
Academic Article Molecular genetic advances in tuberous sclerosis.
Academic Article Human profilin. Molecular cloning, sequence comparison, and chromosomal analysis.
Academic Article The human actin-regulatory protein cap G: gene structure and chromosome location.
Concept Chromosome Breakpoints
Concept Chromosome Walking
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 14
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 4
Concept Chromosome Banding
Concept Chromosome Breakage
Concept Chromosomes, Human, Pair 8
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 2
Concept X Chromosome
Concept Chromosomes, Human, Pair 9
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 16
Concept Chromosome Disorders
Concept Chromosomes, Human, Pair 17
Academic Article Identification of nine genomic regions of amplification in urothelial carcinoma, correlation with stage, and potential prognostic and therapeutic value.
Academic Article Integrative analysis of 1q23.3 copy-number gain in metastatic urothelial carcinoma.
Academic Article The somatic genomic landscape of chromophobe renal cell carcinoma.
Grant MAP OF HUMAN CHROMOSOME 9
Grant INTERNATIONAL WORKSHOP ON HUMAN CHROMOSOME 9
Search Criteria
  • Chromosomes Human Pair 9
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.