Search Results - "Sharma, Anahita"

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  1. 1

    Guiding Oligodendrocyte Precursor Cell Maturation With Urokinase Plasminogen Activator-Degradable Elastin-like Protein Hydrogels by Meco, Edi, Zheng, W. Sharon, Sharma, Anahita H, Lampe, Kyle J

    Published in Biomacromolecules (14-12-2020)
    “…Demyelinating injuries and diseases, like multiple sclerosis, affect millions of people worldwide. Oligodendrocyte precursor cells (OPCs) have the potential to…”
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    Journal Article
  2. 2

    Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment by Pettigrew, Kerry A, Reeves, Emily, Leavett, Ruth, Hayiou-Thomas, Marianna E, Sharma, Anahita, Simpson, Nuala H, Martinelli, Angela, Thompson, Paul, Hulme, Charles, Snowling, Margaret J, Newbury, Dianne F, Paracchini, Silvia

    Published in PloS one (11-08-2015)
    “…A significant proportion of children (up to 7% in the UK) present with pronounced language difficulties that cannot be explained by obvious causes like other…”
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    Journal Article
  3. 3

    Deep Learning for Predicting Pediatric Crohn's Disease Using Histopathological Imaging by Sharma, Anahita H., Lawlor, Burke W., Wang, Jason Y., Sharma, Yash, Sengupta, Saurav, Fernandes, Philip, Zulqarnain, Fatima, May, Eve, Syed, Sana, Brown, Donald E.

    “…The current gold standard for Crohn's disease diagnosis involves the examination of biopsied tissue by a trained physician. However, endoscopic images and…”
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    Conference Proceeding
  4. 4

    Multi‐scale Computational Model of Endothelial Cell‐Pericyte Coupling in Idiopathic Pulmonary Fibrosis by Leonard‐Duke, Julie, Hung, Claire, Sharma, Anahita, Peirce, Shayn M.

    Published in The FASEB journal (01-05-2022)
    “…Introduction Microvascular stability is highly dependent on endothelial cell‐pericyte coupling. In fibrotic diseases, such as idiopathic pulmonary fibrosis…”
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    Journal Article
  5. 5

    Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment: e0134997 by Pettigrew, Kerry A, Reeves, Emily, Leavett, Ruth, Hayiou-Thomas, Marianna E, Sharma, Anahita, Simpson, Nuala H, Martinelli, Angela, Thompson, Paul, Hulme, Charles, Snowling, Margaret J

    Published in PloS one (01-08-2015)
    “…A significant proportion of children (up to 7% in the UK) present with pronounced language difficulties that cannot be explained by obvious causes like other…”
    Get full text
    Journal Article