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XB-GENEPAGE-1014310
Papers associated with cop1
Results 1 - 3 of 3 results
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Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly., Macken WL, Godwin A, Wheway G, Stals K, Nazlamova L, Ellard S, Alfares A, Aloraini T, AlSubaie L, Alfadhel M, Alajaji S, Wai HA, Self J, Douglas AGL, Kao AP, Guille M, Baralle D., Genome Med. February 25, 2021; 13 (1): 34.  |
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Mammalian tribbles homologs at the crossroads of endoplasmic reticulum stress and Mammalian target of rapamycin pathways., Cunard R., Scientifica (Cairo). January 1, 2013; 2013 750871.  |
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Phosphorylation and function of alpha4beta2 receptor., Bermudez I, Moroni M., J Mol Neurosci. January 1, 2006; 30 (1-2): 97-8. |
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