C. Ding

发表

Analysis of the GCM2 gene in isolated hypoparathyroidism: a molecular and biochemical study.

A. Maret, C. Ding, Sara L. Kornfield, 2008, The Journal of clinical endocrinology and metabolism.

Reduction in Gsα Induces Osteogenic Differentiation in Human Mesenchymal Stem Cells

D. Cooke, C. Ding, M. Levine, 2005 .

Reduction in Gsalpha induces osteogenic differentiation in human mesenchymal stem cells.

D. Cooke, C. Ding, M. Levine, 2005, Clinical orthopaedics and related research.

Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1.

A. Maret, C. Ding, M. Levine, 2003, American journal of human genetics.

Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.

B. Buckingham, C. Ding, M. Levine, 2001, The Journal of clinical investigation.

Tropical rickets in Nigeria: Mutation of the CYP2R1 gene encoding vitamin D 25-hydroxylase as a cause of vitamin D dependent rickets

Ravinder J. Singh, C. Ding, M. Levine, 2007 .

Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a.

M. Saji, M. Ringel, C. Ding, 2002, Biochemical and biophysical research communications.

Expression of GCMB by intrathymic parathyroid hormone-secreting adenomas indicates their parathyroid cell origin.

W. Westra, A. Maret, C. Ding, 2004, The Journal of clinical endocrinology and metabolism.

Madelung-like deformity in pseudohypoparathyroidism type 1b.

G. Berkovitz, C. Ding, M. Levine, 2011, The Journal of clinical endocrinology and metabolism.

Cloning and widespread distribution of the rat rod-type cyclic nucleotide-gated cation channel.

S. Guggino, C. Ding, M. Levine, 1997, The American journal of physiology.

Biological changes of myoepithelial cells in atrophic glands after ligation of parotid duct

C. Ding, J. Zuo, Duowen Liu, 2016 .

Pseudohypoparathyroidism 1b: exclusion of parathyroid hormone and its receptors as candidate disease genes.

T. Usdin, M. Labuda, C. Ding, 2000, The Journal of clinical endocrinology and metabolism.

A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia.

T. Jap, C. Ding, M. Levine, 2009, The Journal of clinical endocrinology and metabolism.

The HDR syndrome : an example of a complex developmental disorder associated with hypoparathyroidism Brief report

R. McWilliams, C. Ding, M. Levine, 2005 .

The HDR syndrome: an example of a complex developmentaldisorder associated with hypoparathyroidism

R. McWilliams, C. Ding, M. Levine, 2004 .

cGMP stimulates sodium and chloride currents in rat tracheal airway epithelia.

E. Schwiebert, W. Guggino, S. Guggino, 1997, The American journal of physiology.

A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.

C. Ding, M. Levine, S. Lietman, 2005, The Journal of bone and joint surgery. American volume.

Human rod cGMP-gated cation channel gene maps to 4p12-->centromere by chromosomal in situ hybridization.

E. Jabs, C. Griffin, A. Hawkins, 1993, Genomics.