Search Results - "Balasubramanian, Karthika"

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  1. 1

    Genes uniquely expressed in human growth plate chondrocytes uncover a distinct regulatory network by Li, Bing, Balasubramanian, Karthika, Krakow, Deborah, Cohn, Daniel H

    Published in BMC genomics (20-12-2017)
    “…Chondrogenesis is the earliest stage of skeletal development and is a highly dynamic process, integrating the activities and functions of transcription…”
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    Journal Article
  2. 2

    MED resulting from recessively inherited mutations in the gene encoding calcium‐activated nucleotidase CANT1 by Balasubramanian, Karthika, Li, Bing, Krakow, Deborah, Nevarez, Lisette, Ho, Patric J., Ainsworth, Julia A., Nickerson, Deborah A., Bamshad, Michael J., Immken, LaDonna, Lachman, Ralph S., Cohn, Daniel H.

    “…Multiple Epiphyseal Dysplasia (MED) is a relatively mild skeletal dysplasia characterized by mild short stature, joint pain, and early‐onset osteoarthropathy…”
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    Journal Article
  3. 3

    Achondroplasia with Polydactyly: A Case Report by Frank, Caroline, Shariff, Sameeya, Pavani, Muddepalle, Karthika, Balasubramanian, Thathekalva, Sridhar

    “…An eight-year-old girl child reported to the Department of Oral Medicine and Radiology with the chief complaint of unerupted permanent teeth for past two…”
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    Journal Article
  4. 4

    The Identification and Characterization of Chondrodysplasias Resulting from Cartilage Extracellular Matrix Abnormalities by Balasubramanian, Karthika

    Published 2017
    “…The chondrodysplasias are a group of genetic disorders resulting from profound defects in cartilage development. Two mild chondrodysplasias, Multiple…”
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    Dissertation
  5. 5

    Achondroplasia with Polydactyly: A Case Report by Frank, Caroline, Shariff, Sameeya, Pavani, Muddepalle, Karthika, Balasubramanian, Thathekalva, Sridhar

    “…An eight-year-old girl child reported to the Department of Oral Medicine and Radiology with the chief complaint of unerupted permanent teeth for past two…”
    Get full text
    Journal Article
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    Search for an association between single nucleotide polymorphisms of NPY2R and metabolic syndrome traits by Balasubramanian, Karthika

    Published 01-01-2010
    “…Metabolic syndrome, which characterizes an individual’s risk for cardiovascular disease and type II diabetes mellitus, can be characterized by risk factors…”
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    Dissertation
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