Search Results - "Sunden, S L"

A genetic linkage map for cattle by Bishop, M.D, Kappes, S.M, Keele, J.W, Stone, R.T, Sunden, S.L.F, Hawkins, G.A, Solinas Toldo, S, Fries, R, Grosz, M.D, Yoo, J, Beattie, C.W

“…We report the most extensive physically anchored linkage map for cattle produced to date. Three-hundred thirteen genetic markers ordered in 30 linkage groups,…”
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Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping by Sheffield, V C, Carmi, R, Kwitek-Black, A, Rokhlina, T, Nishimura, D, Duyk, G M, Elbedour, K, Sunden, S L, Stone, E M

“…Bardet-Biedl syndrome is an autosomal recessive disorder characterized by mental retardation, obesity, retinitis pigmentosa, polydactyly and hypogonadism…”
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Identification of a Gene That Causes Primary Open Angle Glaucoma by Stone, Edwin M., Fingert, John H., Wallace L. M. Alward, Nguyen, Thai D., Polansky, Jon R., Sara L. F. Sunden, Nishimura, Darryl, Clark, Abbot F., Nystuen, Arne, Nichols, Brian E., Mackey, David A., Ritch, Robert, Kalenak, Jeffrey W., Craven, E. Randy, Sheffield, Val C.

“…Glaucoma is a major cause of blindness and is characterized by progressive degeneration of the optic nerve and is usually associated with elevated intraocular…”
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A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps by Sheffield, V C, Weber, J L, Buetow, K H, Murray, J C, Even, D A, Wiles, K, Gastier, J M, Pulido, J C, Yandava, C, Sunden, S L

“…We report a collection of tri- and tetranucleotide repeat sequence polymorphic markers used to construct genome-wide human linkage maps. Using a strategy of…”
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Linkage of posterior polymorphous corneal dystrophy to 20q11 by Héon, E, Mathers, W D, Alward, W L, Weisenthal, R W, Sunden, S L, Fishbaugh, J A, Taylor, C M, Krachmer, J H, Sheffield, V C, Stone, E M

“…Posterior polymorphous dystrophy (PPMD) is an autosomal dominant disorder of the cornea that is clinically recognized by the presence of vesicles on the…”
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Linkage of bovine erythrocyte antigen loci B, C, L, S, Z, R' and T' and the serum protein loci post-transferrin 2 (PTF 2), vitamin D binding protein (GC) and albumin (ALB) to DNA microsatellite markers by Kappes, S M, Bishop, M D, Keele, J W, Penedo, M C, Hines, H C, Grosz, M D, Hawkins, G A, Stone, R T, Sunden, S L, Beattie, C W

“…Seven bovine erythrocyte antigen loci and three serum protein loci were tentatively assigned to chromosomes or synteny groups by linkage analysis to previously…”
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Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes by Sunden, S L, Alward, W L, Nichols, B E, Rokhlina, T R, Nystuen, A, Stone, E M, Sheffield, V C

“…Juvenile Open Angle Glaucoma (GLC1A) is an autosomal optic neuropathy that has been localized previously to chromosome 1q. Here we report the fine mapping of…”
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The Booroola fecundity (FecB) gene maps to sheep chromosome 6 by Montgomery, G W, Lord, E A, Penty, J M, Dodds, K G, Broad, T E, Cambridge, L, Sunden, S L, Stone, R T, Crawford, A M

“…The Booroola (FecB) mutation in sheep is linked to markers from a region of syntenic homology to human chromosome HSA4q, but the chromosomal location in sheep…”
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Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25) by Héon, E, Sheth, B P, Kalenak, J W, Sunden, S L, Streb, L M, Taylor, C M, Alward, W L, Sheffield, V C, Stone, E M

“…Iris hypoplasia is an autosomal dominant disorder which is frequently associated with glaucoma. This glaucoma is usually resistant to medical therapy and can…”
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Sheep linkage mapping: nineteen linkage groups derived from the analysis of paternal half-sib families by Crawford, A.M, Montgomery, G.W, Pierson, C.A, Brown, T, Dodds, K.G, Sunden, S.L.F, Henry, H.M, Ede, A.J, Swarbrick, P.A, Berryman, T, Penty, J.M, Hill, D.F

“…Nineteen linkage groups containing a total of 52 markers have been identified in the sheep genome after typing large paternal half-sib families. The linkage…”
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Chromosomal Assignment of 2900 Tri- and Tetranucleotide Repeat Markers Using NIGMS Somatic Cell Hybrid Panel 2 by Sunden, Sara L.F., Businga, Tom, Beck, John, McClain, Ann, Gastier, Julie M., Pulido, Jacqueline C., Yandava, Chandri Naidu, Brody, Thomas, Ghazizadeh, Jelveh, Weber, James L., Duyk, Geoffrey M., Murray, Jeffrey C., Buetow, Kenneth H., Sheffield, V.C.

“…Two thousand nine hundred and thirty-one tri- and tetranucleotide short tandem repeat polymorphisms (STRPs) developed by the Cooperative Human Linkage Center…”
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Polymorphism in and Localization of the Gene LCP2 (SLP-76) to Chromosome 5q33.1–qter by Sunden, Sara L.F., Carr, Laurie L., Clements, James L., Motto, David G., Koretzky, Gary A.

“…The activation of Src and Syk family cytoplasmic tyrosine kinases is an early and required event in T cell receptor (TCR) signal transduction. One approach to…”
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A highly polymorphic bovine microsatellite locus: BM2113 by Sunden, S L, Stone, R T, Bishop, M D, Kappes, S M, Keele, J W, Beattie, C W

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Betaine–Homocysteine Methyltransferase Expression in Porcine and Human Tissues and Chromosomal Localization of the Human Gene by Sunden, Sara L.F., Renduchintala, Murty S., Park, Eric I., Miklasz, Steven D., Garrow, Timothy A.

“…We have prepared antibodies against porcine liver betaine–homocysteine methyltransferase (BHMT; EC 2.1.1.5) and recently cloned cDNAs encoding the porcine and…”
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A conceptual database model for genomic research by Keele, J W, Wray, J E, Behrens, D W, Rohrer, G A, Sunden, S L, Kappes, S M, Bishop, M D, Stone, R T, Alexander, L J, Beattie, C W

“…We describe a conceptual model for genome databases that facilitates the process of building, maintaining, and disseminating physically anchored genetic…”
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