Search Results - Quek, Debra Q Y

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  1. 1
    Novel Serum and Urinary Metabolites Associated with Diabetic Retinopathy in Three Asian Cohorts

    Novel Serum and Urinary Metabolites Associated with Diabetic Retinopathy in Three Asian Cohorts by Quek, Debra Q. Y., He, Feng, Sultana, Rehena, Banu, Riswana, Chee, Miao Li, Nusinovici, Simon, Thakur, Sahil, Qian, Chaoxu, Cheng, Ching-Yu, Wong, Tien Y., Sabanayagam, Charumathi

    Published in Metabolites
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  2. 2
    Cardiovascular disease and thinning of retinal nerve fiber layer in a multi-ethnic Asian population: the Singapore epidemiology of eye diseases study

    Cardiovascular disease and thinning of retinal nerve fiber layer in a multi-ethnic Asian population: the Singapore epidemiology of eye diseases study by Majithia, Shivani, Quek, Debra Q. Y., Chee, Miao Li, Lim, Zhi Wei, Nusinovici, Simon, Soh, Zhi-Da, Thakur, Sahil, Rim, Tyler Hyungtaek, Sabanayagam, Charumathi, Cheng, Ching-Yu, Tham, Yih-Chung

    Published in Frontiers in medicine
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  3. 3
    Structural basis of omega-3 fatty acid transport across the blood–brain barrier

    Structural basis of omega-3 fatty acid transport across the blood–brain barrier by Cater, Rosemary J., Chua, Geok Lin, Erramilli, Satchal K., Keener, James E., Choy, Brendon C., Tokarz, Piotr, Chin, Cheen Fei, Quek, Debra Q. Y., Kloss, Brian, Pepe, Joseph G., Parisi, Giacomo, Wong, Bernice H., Clarke, Oliver B., Marty, Michael T., Kossiakoff, Anthony A., Khelashvili, George, Silver, David L., Mancia, Filippo

    Published in Nature (London)
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  4. 4
    Structural Insights into the Transport Mechanism of the Human Sodium-dependent Lysophosphatidylcholine Transporter MFSD2A

    Structural Insights into the Transport Mechanism of the Human Sodium-dependent Lysophosphatidylcholine Transporter MFSD2A by Quek, Debra Q.Y., Nguyen, Long N., Fan, Hao, Silver, David L.

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  5. 5
    Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination

    Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination by Harel, Tamar, Quek, Debra Q. Y., Wong, Bernice H., Cazenave-Gassiot, Amaury, Wenk, Markus R., Fan, Hao, Berger, Itai, Shmueli, Dorit, Shaag, Avraham, Silver, David L., Elpeleg, Orly, Edvardson, Shimon

    Published in Neurogenetics
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  6. 6
    The longitudinal association between cognitive impairment and incident visual impairment in a multiethnic Asian population: a prospective cohort study

    The longitudinal association between cognitive impairment and incident visual impairment in a multiethnic Asian population: a prospective cohort study by Vu, Tai Anh, Gupta, Preeti, Leow, Felicia Z Y, Fenwick, Eva K, Man, Ryan E K, Tham, Yih-Chung, Xu, Xin, Quek, Debra Q Y, Qian, Chaoxu, Sabanayagam, Charumathi, Chen, Christopher L H, Wong, Tien Yin, Cheng, Ching-Yu, Lamoureux, Ecosse L

    Published in Age and ageing
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