Hamish S Scott
Hamish S Scott
Center of Cancer Biology
Email verificata su sa.gov.au - Home page
Titolo
Citata da
Citata da
Anno
Positional cloning of the APECED gene
K Nagamine, P Peterson, HS Scott, J Kudoh, S Minoshima, M Heino, ...
Nature genetics 17 (4), 393-398, 1997
13911997
Use of within-array replicate spots for assessing differential expression in microarray experiments
GK Smyth, J Michaud, HS Scott
Bioinformatics 21 (9), 2067-2075, 2005
13882005
TWEAK, a new secreted ligand in the tumor necrosis factor family that weakly induces apoptosis
Y Chicheportiche, PR Bourdon, H Xu, YM Hsu, H Scott, C Hession, ...
Journal of Biological Chemistry 272 (51), 32401-32410, 1997
8311997
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
CN Hahn, CE Chong, CL Carmichael, EJ Wilkins, PJ Brautigan, XC Li, ...
Nature genetics 43 (10), 1012, 2011
4972011
RANK signals from CD4+3 inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla
SW Rossi, MY Kim, A Leibbrandt, SM Parnell, WE Jenkinson, ...
The Journal of experimental medicine 204 (6), 1267-1272, 2007
4482007
A network-biology perspective of microRNA function and dysfunction in cancer
CP Bracken, HS Scott, GJ Goodall
Nature Reviews Genetics 17 (12), 719-732, 2016
4012016
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanismsá…
J Michaud, F Wu, M Osato, GM Cottles, M Yanagida, N Asou, ...
Blood, The Journal of the American Society of Hematology 99 (4), 1364-1372, 2002
3882002
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
MD Lalioti, HS Scott, C Buresi, C Rossier, A Bottani, MA Morris, ...
Nature 386 (6627), 847-851, 1997
3571997
Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis
KE Webster, MK O'Bryan, S Fletcher, PE Crewther, U Aapola, J Craig, ...
Proceedings of the National Academy of Sciences 102 (11), 4068-4073, 2005
3242005
Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22. 3, related to the cytosine-5-methyltransferase 3 gene family
U Aapola, K Shibuya, HS Scott, J Ollila, M Vihinen, M Heino, A Shintani, ...
Genomics 65 (3), 293-298, 2000
3242000
Gene Dosage–limiting Role of Aire in Thymic Expression, Clonal Deletion, and Organ-specific Autoimmunity
A Liston, DHD Gray, S Lesage, AL Fletcher, J Wilson, KE Webster, ...
The Journal of experimental medicine 200 (8), 1015-1026, 2004
3132004
Autoimmune regulator is expressed in the cells regulating immune tolerance in thymus medulla
M Heino, P Peterson, J Kudoh, K Nagamine, A Lagerstedt, V Ovod, ...
Biochemical and biophysical research communications 257 (3), 821-825, 1999
3081999
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients
MC Rosatelli, A Meloni, A Meloni, M Devoto, A Cao, HS Scott, P Peterson, ...
Human genetics 103 (4), 428-434, 1998
2621998
The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein
J Pitkńnen, V Doucas, T Sternsdorf, T Nakajima, S Aratani, K Jensen, ...
Journal of Biological Chemistry 275 (22), 16802-16809, 2000
2532000
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
S Shah, KA Schrader, E Waanders, AE Timms, J Vijai, C Miething, ...
Nature genetics 45 (10), 1226-1231, 2013
2522013
Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen
M Alimohammadi, P Bj÷rklund, ┼ Hallgren, N P÷ntynen, G Szinnai, ...
New England Journal of Medicine 358 (10), 1018-1028, 2008
2402008
Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity
M Irla, S Hugues, J Gill, T Nitta, Y Hikosaka, IR Williams, FX Hubert, ...
Immunity 29 (3), 451-463, 2008
2332008
Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness
HS Scott, J Kudoh, M Wattenhofer, K Shibuya, A Berry, R Chrast, ...
Nature genetics 27 (1), 59-63, 2001
2332001
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
J Kazenwadel, GA Secker, YJ Liu, JA Rosenfeld, RS Wildin, ...
Blood 119 (5), 1283-1291, 2012
2302012
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity
H Mehenni, C Gehrig, J Nezu, A Oku, M Shimane, C Rossier, N Guex, ...
The American Journal of Human Genetics 63 (6), 1641-1650, 1998
2261998
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
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