Histidine

GNAS complex locus ; Homo sapiens







7 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 33512531 Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome. 2021 Apr 23 1
2 17873334 Genetic diagnosis of multiple affected tissues in a patient with McCune-Albright syndrome. 2007 Apr 1
3 15368366 Mutation of the highly conserved Arg165 and Glu168 residues of human Gsalpha disrupts the alphaD-alphaE loop and enhances basal GDP/GTP exchange rate. 2004 Oct 1 2
4 12727968 Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene. 2003 May 1
5 12374458 A novel, complex heterozygous mutation within Gsalpha gene in patient with McCune-Albright syndrome. 2002 Jul 2
6 11272890 A comparative study of fibrous dysplasia and osteofibrous dysplasia with regard to Gsalpha mutation at the Arg201 codon: polymerase chain reaction-restriction fragment length polymorphism analysis of paraffin-embedded tissues. 2000 May 1
7 8126161 An unusual presentation of McCune-Albright syndrome confirmed by an activating mutation of the Gs alpha-subunit from a bone lesion. 1994 Mar 3