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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1950 1
1952 2
1959 1
1962 1
1964 2
1966 2
1968 2
1969 1
1970 1
1971 3
1972 2
1973 2
1975 2
1976 2
1977 5
1978 3
1979 4
1980 8
1981 2
1982 5
1983 7
1984 4
1985 6
1986 8
1987 5
1988 9
1989 2
1990 5
1991 13
1992 10
1993 6
1994 13
1995 7
1996 7
1997 10
1998 16
1999 14
2000 13
2001 14
2002 12
2003 14
2004 13
2005 9
2006 4
2007 6
2008 5
2009 2
2010 1
2011 4
2014 1
2017 1
2024 0

Text availability

Article attribute

Article type

Publication date

PubMed (OMIM) for id: 2778

289 results

Results by year

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Page 1
Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome.
Sato Y, Maekawa S, Ishii R, Sanada M, Morikawa T, Shiraishi Y, Yoshida K, Nagata Y, Sato-Otsubo A, Yoshizato T, Suzuki H, Shiozawa Y, Kataoka K, Kon A, Aoki K, Chiba K, Tanaka H, Kume H, Miyano S, Fukayama M, Nureki O, Homma Y, Ogawa S. Sato Y, et al. Science. 2014 May 23;344(6186):917-20. doi: 10.1126/science.1252328. Science. 2014. PMID: 24855271
Crystal structure of the β2 adrenergic receptor-Gs protein complex.
Rasmussen SG, DeVree BT, Zou Y, Kruse AC, Chung KY, Kobilka TS, Thian FS, Chae PS, Pardon E, Calinski D, Mathiesen JM, Shah ST, Lyons JA, Caffrey M, Gellman SH, Steyaert J, Skiniotis G, Weis WI, Sunahara RK, Kobilka BK. Rasmussen SG, et al. Nature. 2011 Jul 19;477(7366):549-55. doi: 10.1038/nature10361. Nature. 2011. PMID: 21772288 Free PMC article.
Gastrointestinal polyps in McCune Albright syndrome.
Zacharin M, Bajpai A, Chow CW, Catto-Smith A, Stratakis C, Wong MW, Scott R. Zacharin M, et al. J Med Genet. 2011 Jul;48(7):458-61. doi: 10.1136/jmg.2010.086330. Epub 2011 Feb 28. J Med Genet. 2011. PMID: 21357941 Free PMC article.
Unusual types of hyperthyroidism.
Hamilton CR Jr, Maloof F. Hamilton CR Jr, et al. Medicine (Baltimore). 1973 May;52(3):195-215. doi: 10.1097/00005792-197305000-00002. Medicine (Baltimore). 1973. PMID: 20407411 Review. No abstract available.
Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gs{alpha} coding mutations and GNAS imprinting defects.
Lecumberri B, Fernández-Rebollo E, Sentchordi L, Saavedra P, Bernal-Chico A, Pallardo LF, Bustos JM, Castaño L, de Santiago M, Hiort O, Pérez de Nanclares G, Bastepe M. Lecumberri B, et al. J Med Genet. 2010 Apr;47(4):276-80. doi: 10.1136/jmg.2009.071001. Epub 2009 Oct 26. J Med Genet. 2010. PMID: 19858129 Free PMC article.
Association of the GNAS locus with severe malaria.
Auburn S, Diakite M, Fry AE, Ghansah A, Campino S, Richardson A, Jallow M, Sisay-Joof F, Pinder M, Griffiths MJ, Peshu N, Williams TN, Marsh K, Molyneux ME, Taylor TE, Koram KA, Oduro AR, Rogers WO, Rockett KA, Haldar K, Kwiatkowski DP. Auburn S, et al. Hum Genet. 2008 Dec;124(5):499-506. doi: 10.1007/s00439-008-0575-8. Epub 2008 Oct 26. Hum Genet. 2008. PMID: 18951142 Free PMC article.
289 results