Search Results - "Halsey, Karin E."

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  1. 1

    Math5 expression and function in the central auditory system by Saul, Sara M., Brzezinski, Joseph A., Altschuler, Richard A., Shore, Susan E., Rudolph, Dellaney D., Kabara, Lisa L., Halsey, Karin E., Hufnagel, Robert B., Zhou, Jianxun, Dolan, David F., Glaser, Tom

    Published in Molecular and cellular neuroscience (01-01-2008)
    “…The basic helix–loop–helix (bHLH) transcription factor Math5 ( Atoh7) is required for retinal ganglion cell (RGC) and optic nerve development. Using Math5-lacZ…”
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    Journal Article
  2. 2

    Hearing dysfunction in heterozygous Mitf(Mi-wh) /+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome by Ni, Christina, Zhang, Deming, Beyer, Lisa A, Halsey, Karin E, Fukui, Hideto, Raphael, Yehoash, Dolan, David F, Hornyak, Thomas J

    Published in Pigment cell and melanoma research (01-01-2013)
    “…The human deafness-pigmentation syndromes, Waardenburg syndrome (WS) type 2a, and Tietz syndrome are characterized by profound deafness but only partial…”
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    Journal Article
  3. 3

    Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome by Hurd, Elizabeth A., Adams, Meredith E., Layman, Wanda S., Swiderski, Donald L., Beyer, Lisa A., Halsey, Karin E., Benson, Jennifer M., Gong, Tzy-Wen, Dolan, David F., Raphael, Yehoash, Martin, Donna M.

    Published in Hearing research (01-12-2011)
    “…Heterozygous mutations in the gene encoding chromodomain-DNA-binding-protein 7 (CHD7) cause CHARGE syndrome, a multiple anomaly condition which includes…”
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    Journal Article
  4. 4

    Hearing dysfunction in heterozygous MitfMi-wh/+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome by Ni, Christina, Zhang, Deming, Beyer, Lisa A., Halsey, Karin E., Fukui, Hideto, Raphael, Yehoash, Dolan, David F., Hornyak, Thomas J.

    Published in Pigment cell and melanoma research (01-01-2013)
    “…Summary The human deafness‐pigmentation syndromes, Waardenburg syndrome (WS) type 2a, and Tietz syndrome are characterized by profound deafness but only…”
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    Journal Article
  5. 5

    Hearing dysfunction in heterozygous M itf Mi‐wh /+ mice, a model for W aardenburg syndrome type 2 and T ietz syndrome by Ni, Christina, Zhang, Deming, Beyer, Lisa A., Halsey, Karin E., Fukui, Hideto, Raphael, Yehoash, Dolan, David F., Hornyak, Thomas J.

    Published in Pigment cell and melanoma research (01-01-2013)
    “…The human deafness‐pigmentation syndromes, Waardenburg syndrome ( WS ) type 2a, and T ietz syndrome are characterized by profound deafness but only partial…”
    Get full text
    Journal Article