Search Results - "Stinard, Philip"

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    Maize opaque5 Encodes Monogalactosyldiacylglycerol Synthase and Specifically Affects Galactolipids Necessary for Amyloplast and Chloroplast Function by Myers, Alan M., James, Martha G., Lin, Qiaohui, Yi, Gibum, Stinard, Philip S., Hennen-Bierwagen, Trade A., Becraft, Philip W.

    Published in The Plant cell (01-06-2011)
    “…The maize (Zea mays) opaque5 (o5) locus was shown to encode the monogalactosyldiacylglycerol synthase MGD1. Null and point mutations of o5 that affect the…”
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    CRINKLY4: A TNFR-Like Receptor Kinase Involved in Maize Epidermal Differentiation by Becraft, Philip W., Stinard, Philip S., McCarty, Donald R.

    “…The maize crinkly4 (cr4) mutation affects leaf epidermis differentiation such that cell size and morphology are altered, and surface functions are compromised,…”
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    Characterization of dull1, a maize gene coding for a novel starch synthase by Gao, M. (National Research Council of Canada, Saskatoon.), Wanat, J, Stinard, P.S, James, M.G, Myers, A.M

    Published in The Plant cell (01-03-1998)
    “…The maize dull1 (du1) gene is a determinant of the structure of endosperm starch, and du1- mutations affect the activity of two enzymes involved in starch…”
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    Maize enr System of r1 Haplotype-Specific Aleurone Color Enhancement Factors by Stinard, Philip S, Kermicle, Jerry L, Sachs, Martin M

    Published in The Journal of heredity (01-03-2009)
    “…We describe a family of 3 dominant r1 haplotype-specific enhancers of aleurone color in Zea mays. Stable alleles of the 3 enhancement of r1 loci (enr1, enr2,…”
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    Spotting factor (Spf) from the Spotted-dilute System in Maize Is a Member of the En/Spm Controlling Element Family by Stinard, Philip S, Sachs, Martin M

    Published in The Journal of heredity (01-09-2005)
    “…The Spotted-dilute controlling element system in maize involves an autonomous Spotting factor (Spf), and a receptor at the r1 locus haplotype R1-r(spotted…”
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    Genetic evidence of mutator-induced deletions in the short arm of chromosome 9 of maize by Robertson, D.S, Stinard, P.S

    Published in Genetics (Austin) (01-02-1987)
    “…Evidence is presented that at least 12 of the Mu-induced yg2 mutants found in an extensive mutation analysis of this locus are the result of deletions in the…”
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    Genetic isolation, cloning, and analysis of a Mutator-induced, dominant antimorph of the maize amylose extender1 locus by Stinard, P.S, Robertson, D.S, Schnable, P.S

    Published in The Plant cell (01-11-1993)
    “…We report the genetic identification, molecular cloning, and characterization of a dominant mutant at the amylose extender1 locus, Ae1-5180. The identities of…”
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    Molecular analysis of viviparous-1: an abscisic acid-insensitive mutant of maize by McCarty, D.R. (University of Florida, Gainesville, FL), Carson, C.B, Stinard, P.S, Robertson, D.S

    Published in The Plant cell (01-05-1989)
    “…The viviparous-1 (vp1) gene in maize controls multiple developmental responses associated with the maturation phase of seed formation. Most notably, mutant…”
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    Crinkyl4: A TNFR-like receptor kinase involved in maize epidermal differentiation by Becraft, Philip W, Stinard, Philip S, McCarty, Donald R

    “…The maize crinkly4 (cr4) mutation affects leaf epidermis differentiation such that cell size and morphology are altered, and surface functions are compromised,…”
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    Journal Article
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    Genetic analysis of 63 mutations affecting maize kernal development isolated from Mutator stocks by Scanlon, Michael J, Stinard, Philip S, James, Martha G, Myers, Alan M, Robertson, Donald S

    Published in Genetics (Austin) (01-01-1994)
    “…Sixty-three mutations affecting development of the maize kernel were isolated from active Robertson's Mutator (Mu) stocks. At least 14 previously undescribed…”
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    Genetic evidence of Mutator-induced deletions in the short arm of chromosome 9 of maize. II. wd deletions by Robertson, D.S, Stinard, P.S, Maguire, M.P

    Published in Genetics (Austin) (01-03-1994)
    “…Analyses of 113 putative Mutator-induced events involving the yg2 locus of chromosome 9 revealed that 11 of these events were deletions that produce albino…”
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