ExLibris header image
SFX Logo
Title: Three distinct genes in human DNA related to the transforming genes of mammalian sarcoma retroviruses
Source:

Science [0036-8075] Wong Staal, F yr:1981


Collapse list of basic services Basic
Sorry, no full text available...
Please use the document delivery service (see below)  
Holding information
Holdings in library search engine ALBERT GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Aoki, Y. "Germline mutations in HRAS proto-oncogene cause Costello syndrome." Nature genetics 37.10 (2005): 1038-1040. Link to Full Text for this item Link to SFX for this item
2. Siegel, D.H. H. "Dermatological phenotype in Costello syndrome: consequences of Ras dysregulation in development." British journal of dermatology 166.3 (2012): 601-607. Link to Full Text for this item Link to SFX for this item
3. Cooper, G M M. "Cellular transforming genes." Science 217.4562 (1982): 801-6. Link to SFX for this item
4. Digilio, M Cristina C. "Costello syndrome: clinical diagnosis in the first year of life." European journal of pediatrics 167.6 (2008): 621-8. Link to SFX for this item
5. Kerr, B. "Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases." Journal of medical genetics 43.5 (2006): 401-405. Link to Full Text for this item Link to SFX for this item
6. van Steensel, M A M A. "Recurring HRAS mutation G12S in Dutch patients with Costello syndrome." Experimental dermatology 15.9 (2006): 731-4. Link to Full Text for this item Link to SFX for this item
7. Gripp, Karen W W. "HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation." American journal of medical genetics. Part A 140 A.1 (2006): 1-7. Link to SFX for this item
8. Rauen, K. "HRAS and the Costello syndrome." Clinical genetics 71.2 (2007): 101-8. Link to Full Text for this item Link to SFX for this item
9. Gripp, Karen W W. "Tumor predisposition in Costello syndrome." American journal of medical genetics. Part C, Seminars in medical genetics 137.1 (2005): 72-7. Link to Full Text for this item Link to SFX for this item
10. Sekhar, Konjet R. "Nrf2 degradation by the ubiquitin proteasome pathway is inhibited by KIAA0132, the human homolog to INrf2." Oncogene 21.44 (2002): 6829-6834. Link to Full Text for this item Link to SFX for this item
11. Nguyen, V. "Cutaneous manifestations of Costello syndrome." International journal of dermatology 46.1 (2007): 72-6. Link to Full Text for this item Link to SFX for this item
12. Estep, Anne L L. "HRAS mutations in Costello syndrome: Detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy." American journal of medical genetics. Part A 140A.1 (2006): 8-16. Link to SFX for this item
13. Quezada, E. "Costello syndrome and related disorders." Current opinion in pediatrics 19.6 (2007): 636-644. Link to SFX for this item
14. Hennekam, RCM. "Costello syndrome: An overview." American journal of medical genetics 117C.1 (2003): 42-48. Link to SFX for this item
15. Rauen, Katherine A A. "Molecular aspects, clinical aspects and possible treatment modalities for Costello syndrome: Proceedings from the 1st International Costello Syndrome Research Symposium 2007." American journal of medical genetics. Part A 146A.9 (2008): 1205-17. Link to SFX for this item
16. Lee, C K K. "Spinal deformities in Noonan syndrome: a clinical review of sixty cases." Journal of bone and joint surgery. American volume 83-A.10: 1495-502. Link to SFX for this item
17. Galera, C. "Evaluation of the behavioural phenotype and the temperament of children with Costello Syndrome." Journal of intellectual disability research (2004): 318-318. Link to Full Text for this item Link to SFX for this item
18. Niihori, T. "HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome." Journal of human genetics 56.10 (2011): 707-715. Link to Full Text for this item Link to SFX for this item
19. Tatano, Y. "Tropoelastin regulates chemokine expression in fibroblasts in Costello syndrome." Biochemical and biophysical research communications 372.4 (2008): 681-7. Link to SFX for this item
20. Leonard, H. "The diagnosis of autism in a female: could it be Rett syndrome?" European journal of pediatrics 167.6 (2008): 661-9. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.