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43 in total

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

Authors: Suzanne Jan de Beur; Changlin Ding; Emily Germain-Lee; Justin Cho; Alexander Maret; Michael A Levine
Journal: Am J Hum Genet Date: 2003-07-11 Impact factor: 11.025

2. A 6-hour human parathyroid hormone (1-34) infusion protocol: studies in normal and hypoparathyroid subjects.

Authors: A McElduff; D Lissner; M Wilkinson; C Cornish; S Posen
Journal: Calcif Tissue Int Date: 1987-11 Impact factor: 4.333

3. Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

Authors: M A Levine; T G Ahn; S F Klupt; K D Kaufman; P M Smallwood; H R Bourne; K A Sullivan; C Van Dop
Journal: Proc Natl Acad Sci U S A Date: 1988-01 Impact factor: 11.205

Review 4. Mutations of signal-transducing G proteins in human disease.

Authors: P Schnabel; M Böhm
Journal: J Mol Med (Berl) Date: 1995-05 Impact factor: 4.599

5. Maintenance of cellular levels of G-proteins: different efficiencies of alpha s and alpha o synthesis in GH3 cells.

Authors: Y Li; U Mende; C Lewis; E J Neer
Journal: Biochem J Date: 1996-09-15 Impact factor: 3.857

Review 6. Pseudohypoparathyroidism and Gsα-cAMP-linked disorders: current view and open issues.

Authors: Giovanna Mantovani; Anna Spada; Francesca Marta Elli
Journal: Nat Rev Endocrinol Date: 2016-04-22 Impact factor: 43.330

7. Functional characterization of GNAS mutations found in patients with pseudohypoparathyroidism type Ic defines a new subgroup of pseudohypoparathyroidism affecting selectively Gsα-receptor interaction.

Authors: Susanne Thiele; Luisa de Sanctis; Ralf Werner; Joachim Grötzinger; Cumhur Aydin; Harald Jüppner; Murat Bastepe; Olaf Hiort
Journal: Hum Mutat Date: 2011-04-12 Impact factor: 4.878

Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism.