Pages that link to "Q41084237"
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The following pages link to A novel mutation adjacent to the switch III domain of G(S alpha) in a patient with pseudohypoparathyroidism (Q41084237):
Displaying 11 items.
- Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS-based heterotopic ossification (Q24654579) (← links)
- Autoinhibition and Signaling by the Switch II Motif in the G-protein Chaperone of a Radical B12 Enzyme (Q27679846) (← links)
- Paternal versus maternal transmission of a stimulatory G-protein alpha subunit knockout produces opposite effects on energy metabolism (Q28593512) (← links)
- Identification of a methylation imprint mark within the mouse Gnas locus (Q33964982) (← links)
- Different biochemical properties explain why two equivalent Gα subunit mutants cause unrelated diseases (Q34070311) (← links)
- A GNAS1 imprinting defect in pseudohypoparathyroidism type IB (Q34457845) (← links)
- A mouse model for osseous heteroplasia (Q34532358) (← links)
- Progressive osseous heteroplasia: diagnosis, treatment, and prognosis (Q35063732) (← links)
- A mutation in the heterotrimeric stimulatory guanine nucleotide binding protein alpha-subunit with impaired receptor-mediated activation because of elevated GTPase activity. (Q35123471) (← links)
- Human G(salpha) mutant causes pseudohypoparathyroidism type Ia/neonatal diarrhea, a potential cell-specific role of the palmitoylation cycle (Q36141479) (← links)
- Cutaneous nodules and a novel GNAS mutation in a Chinese boy with pseudohypoparathyroidism type Ia: A case report and review of literature (Q89942807) (← links)