Search Results - "Sunden, S"

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    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

    Published in Genetics (Austin) (01-02-1994)
    “…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

    Published in Human molecular genetics (01-08-1994)
    “…Bardet-Biedl syndrome is an autosomal recessive disorder characterized by mental retardation, obesity, retinitis pigmentosa, polydactyly and hypogonadism…”
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    Accuracy and precision in the radiographic diagnosis of clinical instability in Brånemark dental implants by Sundén, S, Gröndahl, K, Gröndahl, H G

    Published in Clinical oral implants research (01-12-1995)
    “…The aim was to evaluate accuracy and precision in the radiographic diagnosis of clinical instability in Brånemark dental implants. In two clinics specialized…”
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    Inter- and intraobserver variability in radiographic bone level assessment at Brånemark fixtures by Gröndahl, Kerstin, Sundén, Solweig, Gröndahl, Hans-göran

    Published in Clinical oral implants research (01-08-1998)
    “…The aim was to determine inter‐ and intraobserver variability in radiographic bone level assessments at Brånemark fixtures and to study the influence of…”
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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

    Published in Human molecular genetics (01-10-1995)
    “…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

    Published in Human molecular genetics (01-03-1995)
    “…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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    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

    Published in Genomics (San Diego, Calif.) (01-07-1994)
    “…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

    Published in Human molecular genetics (01-08-1995)
    “…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

    Published in Genetics (Austin) (01-06-1994)
    “…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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    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

    Published in Genome research (01-09-1996)
    “…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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    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

    Published in Animal genetics (01-06-1994)
    “…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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    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

    Published in Journal of computational biology (1994)
    “…We describe a conceptual model for genome databases that facilitates the process of building, maintaining, and disseminating physically anchored genetic…”
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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.

    Published in Genomics (San Diego, Calif.) (01-07-1996)
    “…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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    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.

    Published in Archives of biochemistry and biophysics (01-09-1997)
    “…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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    Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers by Gastier, J M, Pulido, J C, Sunden, S, Brody, T, Buetow, K H, Murray, J C, Weber, J L, Hudson, T J, Sheffield, V C, Duyk, G M

    Published in Human molecular genetics (01-10-1995)
    “…Genetic markers based upon PCR amplification of short tandem repeat-containing sequence tagged sites (STSs) have become the standard for genetic mapping. We…”
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