Search Results - "Golden, Wendy L."

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  1. 1

    Development and characterization of xenograft model systems for adenoid cystic carcinoma by Moskaluk, Christopher A, Baras, Alexander S, Mancuso, Stefani A, Fan, Hao, Davidson, Robert J, Dirks, Dawn C, Golden, Wendy L, Frierson, Henry F

    Published in Laboratory investigation (01-10-2011)
    “…Adenoid cystic carcinoma (ACC) is one of the most common malignancies to arise in human salivary glands, and it also arises in the glandular tissue of other…”
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    A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome by Baxter, Adrianne L., Vivian, Jay L., Hagelstrom, R. Tanner, Hossain, Waheeda, Golden, Wendy L., Wassman, E. Robert, Vanzo, Rena J., Butler, Merlin G.

    Published in Molecular syndromology (01-06-2017)
    “…Mowat-Wilson syndrome is a rare genetic condition characterized by intellectual disability, structural anomalies, and dysmorphic features. It is caused by…”
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    Phase determination using chromosomal microarray and fluorescence in situ hybridization in a patient with early onset Parkinson disease and two deletions in PRKN by Williams, Eli S., Barrett, Matthew J., Dhamija, Radhika, Toran, Lisa, Chambers, Chelsea, Mahadevan, Mani S., Golden, Wendy L.

    Published in Molecular genetics & genomic medicine (01-05-2018)
    “…Background Mutations in the parkin gene (PRKN) are the most commonly identified genetic factors in early onset Parkinson disease (EOPD), with biallelic…”
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    Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene by Huang, Taosheng, Lin, Angela E., Cox, Gerald F., Golden, Wendy L., Feldman, Gerald L., Ute, Moog, Schrander-Stumpel, Connie, Kamisago, Mitsuhiro, Vermeulen, Stefan J.T.

    Published in Genetics in medicine (01-11-2002)
    “…Purpose: Terminal deletions of chromosome 4q are commonly associated with cardiovascular malformations (CVMs). The dHAND gene (HAND2, heart and neural crest…”
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    Trilateral retinoblastoma variant indicative of the relevance of the retinoblastoma tumor-suppressor pathway to medulloblastomas in humans: Case report by ELIAS, W. Jeffrey, LOPES, M. Beatriz S, GOLDEN, Wendy L, JANE, John A, GONZALEZ-FERNANDEZ, Federico

    Published in Journal of neurosurgery (01-11-2001)
    “…✓ Results of recent studies have led investigators to suggest that the retinoblastoma tumor-suppressor (rb) gene plays an underappreciated role in the genesis…”
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    Acquisition of acoustic startle shows a dose-response to serum free T4 by Schneider, B F, Golden, W L

    “…Methimazole, administered to rats in drinking water (0.1 and 0.05%) from embryonic day 17 to postnatal day 10, caused a dose-dependent decrease in serum Free…”
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    Genetic and phenotypic changes associated with the acquisition of tumorigenicity in human bladder cancer by Gildea, John J., Golden, Wendy L., Harding, Michael A., Theodorescu, Dan

    Published in Genes chromosomes & cancer (01-03-2000)
    “…There has been a general lack of human paired cell lines that both reproduce the in vivo spectrum of tumor progression of bladder cancer and have some of the…”
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    Acquisition of acoustic startle response in relation to growth and thyroid function in rats by Schneider, B F, Golden, W L

    “…Thiourea was administered by gavage to pregnant and lactating rats from gestational day 18 until postnatal day 10, at doses of 100 or 250 mg per day…”
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    Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa by WESTBROOK, V. A, DIEKMAN, A. B, FLICKINGER, C. J, HERR, J. C, KLOTZ, K. L, KHOLE, V. V, VON KAP-HERR, C, GOLDEN, W. L, EDDY, R. L, SHOWS, T. B, STOLER, M. H, LEE, C.-Y. G

    Published in Biology of reproduction (01-08-2000)
    “…Formation of mature spermatozoa involves a series of dramatic molecular and morphological changes in the male germ cell lineage. These changes result from the…”
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    Trilateral retinoblastoma variant indicative of the relevance of the retinoblastoma tumor-suppressor pathway to medulloblastomas in humans by Elias, W J, Lopes, M B, Golden, W L, Jane, Sr, J A, Gonzalez-Fernandez, F

    Published in Journal of neurosurgery (01-11-2001)
    “…Results of recent studies have led investigators to suggest that the retinoblastoma tumor-suppressor (rb) gene plays an underappreciated role in the genesis of…”
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    Discordant phenotypes and 45,X/46,X,idic(Y) by Kelly, T E, Franko, J B, Rogol, A, Golden, W L

    Published in Journal of medical genetics (01-10-1998)
    “…Mosaicism introduces wide variability into the clinical expression of numerical and unbalanced structural chromosomal abnormalities. The phenotypic range of…”
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    Gonadoblastomas in 45,X/46,XY mosaicism: Analysis of Y chromosome distribution by fluorescence in situ hybridization by IEZZONI, J. C, VON KAP-HERR, C, GOLDEN, W. L, GAFFEY, M. J

    Published in American journal of clinical pathology (01-08-1997)
    “…Gonadoblastomas are composed of nests of neoplastic germ cells and sex cord derivatives surrounded by ovarian-type stroma. These tumors are found almost…”
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    Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa1 by Westbrook, V. Anne, Diekman, Alan B, Klotz, Ken L, Khole, Vrinda V, Kap-Herr, Chris von, Golden, Wendy L, Eddy, Roger L, Shows, Thomas B, Stoler, Mark H, G. Lee, Chi-Yu, Flickinger, Charles J, Herr, John C

    Published in Biology of reproduction (01-08-2000)
    “…Formation of mature spermatozoa involves a series of dramatic molecular and morphological changes in the male germ cell lineage. These changes result from the…”
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    Human fertilin β: Identification, characterization, and chromosomal mapping of an ADAM gene family member by Vidaeus, Cecilia M., von Kap-Herr, Chris, Golden, Wendy L., Eddy, Roger L., Shows, Thomas B., Herr, John C.

    Published in Molecular reproduction and development (01-03-1997)
    “…Fertilin α/β (PH30 α/β) is a heterodimeric sperm surface protein containing binding and fusion domains with potential for interaction with integrin receptors…”
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    Malignant rhabdoid tumor of the kidney: involvement of chromosome 22 by Shashi, V, Lovell, M A, von Kap-herr, C, Waldron, P, Golden, W L

    Published in Genes chromosomes & cancer (01-05-1994)
    “…Cytogenetic and molecular studies have demonstrated that involvement of 22q is a non-random finding in malignant rhabdoid tumors (MRTs) of the brain. We…”
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