Search Results - "Tomfohrde, J."

Breastfeeding mothers' use of technology while breastfeeding by Tomfohrde, Olivia J., Reinke, Jennifer S.

“…This study addresses the social media and technology habits of breastfeeding mothers while they are breastfeeding. Data was collected via a Qualtrics survey…”
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High resolution of human evolutionary trees with polymorphic microsatellites by Bowcock, A. M, Ruiz-Linares, A, Tomfohrde, J, Minch, E, Kidd, J. R, Cavalli-Sforza, L. L

“…Genetic variation at hypervariable loci is being used extensively for linkage analysis and individual identification, and may be useful for inter-population…”
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Gene for Familial Psoriasis Susceptibility Mapped to the Distal End of Human Chromosome 17q by Tomfohrde, James, Silverman, Alan, Barnes, Robert, Fernandez-Vina, Marcelo A., Young, Melodie, Lory, Detra, Morris, Laura, Wuepper, Kirk D., Stastny, Peter, Menter, Alan, Bowcock, Anne

“…A gene involved in psoriasis susceptibility was localized to the distal region of human chromosome 17q as a result of a genome-wide linkage analysis with…”
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A Familial Hypertrophic Cardiomyopathy Locus Maps to Chromosome 15q2 by Thierfelder, Ludwig, MacRae, Calum, Watkins, Hugh, Tomfohrde, James, Williams, Michele, McKenna, William, Bohm, Katarina, Noeske, Gerhard, Schlepper, Martin, Bowcock, Anne, Vosberg, Hans-Peter, Seidman, J. G., Seidman, Christine

“…We report that a gene responsible for familial hypertrophic cardiomyopathy (FHC) in a kindred with a mild degree of cardiac hypertrophy maps to chromosome…”
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A 4.5-Megabase Yeast Artificial Chromosome Contig from Human Chromosome 13q14.3 Ordering 9 Polymorphic Microsatellites (22 Sequence-Tagged Sites) Tightly Linked to the Wilson Disease Locus by White, A., Tomfohrde, J., Stewart, E., Barnes, R., Le Paslier, D., Weissenbach, J., Cavalli-Sforza, L., Farrer, L., Bowcock, A.

“…We have previously performed a genetic analysis of multiply affected families to map a locus responsible for Wilson disease (WND) to a 0.3-centimorgan (cM)…”
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Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites by BOWCOCK, A. M, TOMFOHRDE, J, WEISSENBACH, J, BONNE-TAMIR, B, ST GEORGE-HYSLOP, P, GIAGHEDDU, M, CAVALLI-SFORZA, L. L, FARRER, L. A

“…Wilson disease (WND) is an autosomal recessive disorder that is due to an inability of the liver to eliminate copper. Copper buildup in the liver, brain,…”
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Polymorphic microsatellites and Wilson disease (WD) by STEWART, E. A, WHITE, A, SEO, J. K, LO, W. H.-Y, IVANOVA-SMOLENSKAYA, I. A, LIMBORSKA, S. A, CAVALLI-SFORZA, L. L, FARRER, L. A, BOWCOCK, A. M, TOMFOHRDE, J, OSBORNE-LAWRENCE, S, PRESTRIDGE, L, BONNE-TAMIR, B, SCHEINBERG, I. H, GEORGE-HYSLOP, P. ST, GIAGHEDDU, M, KIM, J.-W

“…Wilson disease (WD), an autosomal recessive disorder of copper metabolism, has been previously mapped to chromosome 13q. Highly informative PCR-based…”
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A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites by Beckmann, J S, Tomfohrde, J, Barnes, R I, Williams, M, Broux, O, Richard, I, Weissenbach, J, Bowcock, A M

“…We have constructed a 2.0 centiMorgan (cM) resolution genetic linkage map for chromosome 15q that contains 55 polymorphic satellites and 3 RFLPs that have…”
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Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors by Tomfohrde, J, Wood, S, Schertzer, M, Wagner, M J, Wells, D E, Parrish, J, Sadler, L A, Blanton, S H, Daiger, S P, Wang, Z

“…A linkage map consisting of 21 dinucleotide repeat polymorphisms, 1 tetranucleotide repeat polymorphism, and 3 RFLPs was constructed for human chromosome 8…”
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JAK3 maps to human chromosome 19p12 within a cluster of protooncogenes and transcription factors by Hoffman, SMG, Siew Lai, K, Tomfohrde, J, Bowcock, A, Gordon, LA, Mohrenweiser, H W

“…JAK3 is the most recently discovered member of a family of cytoplasmic tyrosine kinases (including JAK1, JAK2, and TYK2) of the cytokine receptor signaling…”
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A 4. 5-megabase yeast artificial chromosome contig from human chromosome 13q14. 3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus by White, A., Tomfohrde, J., Barnes, R., Stewart, E., Cavalli-Sforza, L., Le Paslier, D., Weissenbach, J., Farrer, L., Bowcock, A.

“…The authors have previously performed a genetic analysis of multiply affected families to map a locus responsible for Wilson disease (WND) to a 0.3-centimorgan…”
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JAK3 Maps to Human Chromosome 19p12 within a Cluster of Proto-oncogenes and Transcription Factors by Hoffman, Susan M.G., Lai, Koon Siew, Tomfohrde, James, Bowcock, Anne, Gordon, Laurie A., Mohrenweiser, Harvey W.

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A familial hypertropic cardiomyopathy locus maps to chromosome 15q2 by THIERFELDER, L, MACRAE, C, VOSBERG, H.-P, SEIDMAN, J. G, SEIDMAN, C, WATKINS, H, TOMFOHRDE, J, WILLIAMS, M, MCKENNA, W, BOHM, K, NOESKE, G, SCHLEPPER, M, BOWCOCK, A

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Polymorphic microsatellite and Wilson disease (WD) by Stewart, E A, White, A, Tomfohrde, J, Osborne-Lawrence, S, Prestridge, L, Bonne-Tamir, B, Scheinberg, I H, St George-Hyslop, P, Bowcock, A M

“…Wilson disease (WD), an autosomal recessive disorder of copper metabolism, has been previously mapped to chromosome 13q. Highly informative PCR-based…”
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