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Results 1-10 of 27 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2004
Inhibition of generation of cytotoxic T lymphocyte activity by a CCL19/macrophage inflammatory protein (MIP)-3beta antagonist
Pilkington, K.
;
Clark-Lewis, I.
;
McColl, S.
2002
Asparagine hydroxylation of the HIF transactivation domain: A hypoxic switch
Lando, D.
;
Peet, D.
;
Whelan, D.
;
Gorman, J.
;
Whitelaw, M.
2013
The genomic landscape of hypodiploid acute lymphoblastic leukemia
To, L.
2013
A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumption
Chew, T.
;
Peaston, A.
;
Lim, A.
;
Lorthongpanich, C.
;
Knowles, B.
;
Solter, D.
;
Sun, Q.-Y.
2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
Huang, L.
;
Jolly, L.
;
Willis-Owen, S.
;
Gardner, A.
;
Sharma, R.
;
Douglas, E.
;
Shoubridge, C.
;
Wieczorek, D.
;
Tzschach, A.
;
Cohen, M.
;
Hackett, A.
;
Field, M.
;
Froyen, G.
;
Hu, H.
;
Haas, S.
;
Ropers, H.
;
Kalscheuer, V.
;
Corbett, M.
;
Gecz, J.
2003
Nova regulates GABA(A) receptor gamma 2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancer
Dredge, B.
;
Darnell, R.
2014
Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease
Newman, M.
;
Wilson, L.
;
Verdile, G.
;
Lim, A.
;
Khan, I.
;
Nik, S.
;
Pursglove, S.
;
Chapman, G.
;
Martins, R.
;
Lardelli, M.
2006
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
Hagens, O.
;
Dubos, A.
;
Abidi, F.
;
Barbi, G.
;
Van Zutven, L.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Moraine, C.
;
Fryns, J.
;
Chelly, J.
;
van Bokhoven, H.
;
Gecz, J.
;
Dollfus, H.
;
Ropers, H.
;
Schwartz, C.
;
de Cassia Stocco dos Santos, R.
;
Kalscheuer, V.
;
Hanauer, A.
2001
Peptide insertions in domain 4 of hbc, the shared signalling receptor subunit for GM-CSF, IL3 and IL5, induce ligand-independent activation
Jones, K.
;
Bagley, C.
;
Butcher, C.
;
Barry, S.
;
Vadas, M.
;
D'Andrea, R.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
Discover
Author
9
Gecz, J.
5
et al.
4
Corbett, M.
4
Mulley, J.
3
Gardner, A.
3
Kalscheuer, V.
3
Ropers, H.
3
Shaw, M.
3
Thomas, P.
2
Afawi, Z.
.
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Subject
27
Animals
21
Humans
20
Amino Acid Sequence
11
Base Sequence
10
Female
10
Male
9
Pedigree
7
Intellectual Disability
7
Protein Structure, Tertiary
6
Models, Molecular
.
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Date issued
10
2010 - 2014
16
2000 - 2009
1
1998 - 1999