C. Ginter

发表

Transport mechanism of a bacterial homologue of glutamate transporters

N. Reyes, C. Ginter, O. Boudker, 2009, Nature.

Structure and activity of tryptophan-rich TSPO proteins

Wayne A Hendrickson, Burkhard Rost, Edda Kloppmann, 2015, Science.

Molecular analysis of a congenital iodide transport defect: G543E impairs maturation and trafficking of the Na+/I- symporter.

C. Ginter, A. De la Vieja, N. Carrasco, 2005, Molecular endocrinology.

Novel structural features drive DNA binding properties of Cmr, a CRP family protein in TB complex mycobacteria

C. Ginter, M. Cassidy, J. Cheung, 2017, Nucleic acids research.

Journey of the iodide transporter NIS: from its molecular identification to its clinical role in cancer.

C. Ginter, A. De la Vieja, N. Carrasco, 2001, Trends in biochemical sciences.

The Q267E mutation in the sodium/iodide symporter (NIS) causes congenital iodide transport defect (ITD) by decreasing the NIS turnover number

C. Ginter, A. De la Vieja, N. Carrasco, 2004, Journal of Cell Science.

The sodium/iodide Symporter (NIS): characterization, regulation, and medical significance.

C. Ginter, A. De la Vieja, N. Carrasco, 2003, Endocrine reviews.

Na(+)/I(-) symporter activity requires a small and uncharged amino acid residue at position 395.

L. Amzel, C. Ginter, N. Carrasco, 2002, Molecular endocrinology.

Opposite voltage gating polarities of two closely related onnexins

C. Ginter, V. Verselis, T. Bargiello, 1994, Nature.

Structural insights into mis-regulation of protein kinase A in human tumors

R. Darnell, N. Robine, W. Hendrickson, 2015, Proceedings of the National Academy of Sciences.

Characterization of the thyroid Na+/I- symporter with an anti-COOH terminus antibody.

C. Ginter, N. Carrasco, C. Riedel, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Structures of paraoxon‐inhibited human acetylcholinesterase reveal perturbations of the acyl loop and the dimer interface

C. Ginter, M. Cassidy, M. Franklin, 2016, Proteins.

Amino Acid Residues in Transmembrane Segment IX of the Na+/I– Symporter Play a Role in Its Na+ Dependence and Are Critical for Transport Activity*

C. Ginter, A. De la Vieja, N. Carrasco, 2007, Journal of Biological Chemistry.

Conformational ensemble of the sodium coupled aspartate transporter

Jack H. Freed, Elka R. Georgieva, Peter P. Borbat, 2012, Nature Structural &Molecular Biology.

Molecular characterization of V59E NIS, a Na+/I- symporter mutant that causes congenital I- transport defect.

C. Ginter, A. De la Vieja, N. Carrasco, 2008, Endocrinology.

Chemical catalysis by the translocator protein (18 kDa).

C. Ginter, O. Boudker, I. Kiburu, 2013, Biochemistry.

The iodide-transport-defect-causing mutation R124H: a &dgr;-amino group at position 124 is critical for maturation and trafficking of the Na+/I− symporter

C. Ginter, N. Carrasco, V. Paroder, 2013, Journal of Cell Science.

Identification of a structural requirement for thyroid Na+/I− symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism

C. Ginter, A. De la Vieja, O. Levy, 1998, FEBS letters.

Molecular Characterization of V59E NIS, a Na (cid:1) /I (cid:2) Symporter Mutant that Causes Congenital I (cid:2) Transport Defect

C. Ginter, N. Carrasco, A. Vieja, 2008 .

N-linked Glycosylation of the Thyroid Na+/I− Symporter (NIS)

C. Ginter, A. De la Vieja, O. Levy, 1998, The Journal of Biological Chemistry.