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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. , Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
From zebrafish to human: A comparative approach to elucidate the role of the thyroid hormone transporter MCT8 during brain development. , Vancamp P., Gen Comp Endocrinol. September 1, 2018; 265 219-229.
Frogs model man: In vivo thyroid hormone signaling during development. , Sachs LM ., Genesis. January 1, 2017; 55 (1-2):
Involvement of the L-Type Amino Acid Transporter Lat2 in the Transport of 3,3'-Diiodothyronine across the Plasma Membrane. , Kinne A., Eur Thyroid J. September 1, 2015; 4 (Suppl 1): 42-50.
Characterization of thyroid hormone transporter expression during tissue-specific metamorphic events in Xenopus tropicalis. , Connors KA., Gen Comp Endocrinol. August 1, 2010; 168 (1): 149-59.
Establishment and characterization of mammalian cell lines stably expressing human L-type amino acid transporters. , Morimoto E., J Pharmacol Sci. December 1, 2008; 108 (4): 505-16.
Thyroid hormone transport by the heterodimeric human system L amino acid transporter. , Friesema EC., Endocrinology. October 1, 2001; 142 (10): 4339-48.