Search Results - "Witte, S M"

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    Bone ALP and OC reference standards in adult baboons (Papio hamadryas) by sex and age by Havill, L.M., Hale, L.G., Newman, D.E., Witte, S.M., Mahaney, M.C.

    Published in Journal of medical primatology (01-04-2006)
    “…Background  Serum bone‐specific alkaline phosphatase (bone ALP) and intact osteocalcin (OC) are markers of bone formation of interest because of easy…”
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    Journal Article
  3. 3

    Linkage Mapping in Papio Baboons: Conservation of a Syntenic Group of Six Markers on Human Chromosome 1 by Rogers, J., Witte, S.M., Kammerer, C.M., Hixson, J.E., MacCluer, J.W.

    Published in Genomics (San Diego, Calif.) (20-07-1995)
    “…We have established multipoint genetic linkage among six loci in baboons (Papio hamadryas). Published PCR primers designed to amplify five human microsatellite…”
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    A baboon (Papio hamadryas) with an isochromosome for the long arm of the X by Moore, C M, Leland, M M, Brzyski, R G, McKeand, J, Witte, S M, Rogers, J

    Published in Cytogenetics and cell genetics (01-01-1998)
    “…A 5.5-yr-old female baboon was evaluated for sexual immaturity. She was small for her age and had normal external female genitalia. However, she lacked…”
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  5. 5

    Microsatellite variation in two populations of free-ranging yellow baboons (Papio hamadryas cynocephalus) by GEORGE, D. S, WITTE, S. M, TURNER, T. R, WEISS, M. L, PHILLIPS-CONROY, J, SMITH, E. O, ROGERS, J

    Published in International journal of primatology (01-04-1998)
    “…We investigated genetic variation at six microsatellite (simple sequence repeat) loci in yellow baboons (Papio hamadryas cynocephalus) at two localities: the…”
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  6. 6

    Origins of Heterochromatic Repatterning in White-Footed Mice, Peromyscus leucopus by Bowers, Kevin L., Hamilton, Meredith J., Witte, Shelly M., Baker, Robert J.

    Published in Journal of mammalogy (01-08-1998)
    “…There appear to be at least three potential mechanisms to explain karyotypic orthoselection resulting in heterochromatic repatterning in the white-footed…”
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    Teratoma with trisomy 16 in a baboon (Papio hamadryas) by Moore, Charleen M., McKeand, Jennifer, Witte, Shelly M., Hubbard, Gene B., Rogers, Jeffrey, Leland, M. Michelle

    Published in American journal of primatology (1998)
    “…A teratoma was found during a planned cesarean section in a 10‐year‐old primigravida baboon. This teratoma had a female sex chromosome complement and trisomy…”
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  8. 8

    Interspecific variation at the Y-linked RPS4Y locus in hominoids: Implications for phylogeny by Samollow, Paul B., Cherry, Lynn M., Witte, Shelly M., Rogers, Jeffrey

    Published in American journal of physical anthropology (01-11-1996)
    “…Within‐ and between‐species variation in restriction endonuclease recognition sites was examined at the Y‐linked RPS4Y locus of six hominoid species: human…”
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    Gender Identification in Birds Using Microsatellite DNA Fingerprint Analysis by Longmire, Jonathan L., Maltbie, Mary, Robert W. Pavelka, Smith, Loren M., Witte, Shelly M., Ryder, Oliver A., Ellsworth, Darrell L., Baker, Robert J.

    Published in The Auk (01-04-1993)
    “…The inability to identify bird gender in a reliable and noninvasive manner in some birds represents an impediment to captive-propagation programs. The…”
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    Microsatellite polymorphisms in Bolivian squirrel monkeys (Saimiri boliviensis) by Witte, Shelly M., Rogers, Jeffrey

    Published in American journal of primatology (1999)
    “…Two different approaches were used to identify new microsatellite polymorphisms among captive Bolivian squirrel monkeys (Saimiri boliviensis). In the first…”
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    ORIGINAL ARTICLE: Bone ALP and OC reference standards in adult baboons (Papio hamadryas) by sex and age by Havill, L M, Hale, L G, Newman, DE, Witte, S M, Mahaney, M C

    Published in Journal of medical primatology (01-04-2006)
    “…Background: Serum bone-specific alkaline phosphatase (bone ALP) and intact osteocalcin (OC) are markers of bone formation of interest because of easy…”
    Get full text
    Journal Article
  12. 12

    Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition? by Meyer Witte, S, Espil-Taris, C, Cenraud, C, Le Brun, S, Loiseau, H, Chateil, J F, Lacombe, D, Pédespan, J M

    “…Although the pathogenesis of cerebral aneurysms has been studied intensively, it is yet poorly understood. However, a genetic predisposition to this pathology…”
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