Adelaide Research & Scholarship: Search

Search

Results 11-20 of 153 (Search time: 0.003 seconds).

previous
1
2
3
4
5
...
16
next

Item hits:

Preview	Issue Date	Title	Author(s)
	1997	Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident	Wicking, C.; Shanley, S.; Smyth, I.; Gillies, S.; Negus, K.; Graham, S.; Suthers, G.; Haites, N.; Edwards, M.; Wainwright, B.; Chenevix Trench, G.
	1999	Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumors	Hooper, J.; Nicol, D.; Dickinson, J.; Eyre, H.; Scarman, A.; Normyle, J.; Stuttgen, M.; Douglas, M.; Loveland, K.; Sutherland, G.; Antalis, T.
	2008	Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform	Sharma, S.; Burdon, K.; Dave, A.; Jamieson, R.; Yaron, Y.; Billson, F.; van Maldergem, L.; Lorenz, B.; Gecz, J.; Craig, J.
	2007	Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus	Raymond, F.; Tarpey, P.; Edkins, S.; Tofts, C.; O'Meara, S.; Teague, J.; Butler, A.; Stevens, C.; Barthorpe, S.; Buck, G.; Cole, J.; Dicks, E.; Gray, K.; Harrison, R.; Hills, K.; Hinton, J.; Jones, D.; Menzies, A.; Perry, J.; Raine, K.; et al.
	1995	Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization	Eyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N.
	1996	bcl-w, a novel member of the bcl-2 family, promotes cell survival	Gibson, L.; Holmgreen, S.; Huang, D.; Bernand, O.; Copeland, N.; Jenkins, N.; Sutherland, G.; Baker, E.; Adams, J.; Cory, S.
	1999	Regulation of lymphotoxin production by the p21ras-raf-MEK-ERK cascade in PHA/PMA-stimulated Jurkat cells	Li, Y.; Hii, C.; Costabile, M.; Goh, D.; Der, C.; Ferrante, A.
	1996	Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux-Lamy syndrome	Isbrandt, D.; Hopwood, J.; von Figura, K.; Peters, C.
	1998	Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discs	Callaghan, M.; Russell, A.; Woollatt, E.; Sutherland, G.; Sutherland, R.; Watts, C.
	1997	A Novel Epithelial-Expressed ETS Gene, ELF3 - Human and Murine cDNA Sequences, Murine Genomic Organization, Human Mapping to 1q32.2 and Expression in Tissues and Cancer	Tymms, M.; Ng, A.; Thomas, R.; Schutte, B.; Zhou, J.; Eyre, H.; Sutherland, G.; Seth, A.; Rosenberg, M.; Papas, T.; Debouck, C.; Kola, I.