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Results 1-9 of 9 (Search time: 0.006 seconds).
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Issue Date
Title
Author(s)
1998
Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B
Wallace, R.
;
Wang, D.
;
Singh, R.
;
Scheffer, I.
;
George Jnr., A.
;
Phillips, H.
;
Saar, K.
;
Reis, A.
;
Johnson, E.
;
Sutherland, G.
;
Berkovic, S.
;
Mulley, J.
2017
Mapping complex traits in a diversity outbred f1 mouse population identifies germline modifiers of metastasis in human prostate cancer
Winter, J.
;
Gildea, D.
;
Andreas, J.
;
Gatti, D.
;
Williams, K.
;
Lee, M.
;
Hu, Y.
;
Zhang, S.
;
Mullikin, J.
;
Wolfsberg, T.
;
McDonnell, S.
;
Fogarty, Z.
;
Larson, M.
;
French, A.
;
Schaid, D.
;
Thibodeau, S.
;
Churchill, G.
;
Crawford, N.
2015
HENMT1 and piRNA stability are required for adult male germ cell transposon repression and to define the spermatogenic program in the mouse
Lim, S.
;
Qu, Z.
;
Kortschak, R.
;
Lawrence, D.
;
Geoghegan, J.
;
Hempfling, A.
;
Bergmann, M.
;
Goodnow, C.
;
Ormandy, C.
;
Wong, L.
;
Mann, J.
;
Scott, H.
;
Jamsai, D.
;
Adelson, D.
;
O'Bryan, M.
;
Frye, M.
2015
Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity
Moussavi Nik, S.
;
Newman, M.
;
Wilson, L.
;
Ebrahimie, E.
;
Wells, S.
;
Musgrave, I.
;
Verdile, G.
;
Martins, R.
;
Lardelli, M.
2019
DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation patterns
Skvortsova, K.
;
Masle-Farquhar, E.
;
Luu, P.L.
;
Song, J.Z.
;
Qu, W.
;
Zotenko, E.
;
Gould, C.M.
;
Du, Q.
;
Peters, T.J.
;
Colino-Sanguino, Y.
;
Pidsley, R.
;
Nair, S.S.
;
Khoury, A.
;
Smith, G.C.
;
Miosge, L.A.
;
Reed, J.H.
;
Kench, J.G.
;
Rubin, M.A.
;
Horvath, L.
;
Bogdanovic, O.
;
et al.
2011
Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases
Lawlor, K.
;
O'Keefe, L.
;
Samaraweera, S.
;
van Eyk, C.
;
McLeod, C.
;
Maloney, C.
;
Dang, T.
;
Suter, C.
;
Richards, R.
2011
Identification of SOX3 as an XX male sex reversal gene in mice and humans
Sutton, E.
;
Hughes, J.
;
White, S.
;
Sekido, R.
;
Tan, J.
;
Arboleda, V.
;
Rogers, N.
;
Knower, K.
;
Rowley, L.
;
Eyre, H.
;
Rizzoti, K.
;
McAninch, D.
;
Golcalves, J.
;
Slee, J.
;
Turbitt, E.
;
Bruno, D.
;
Bengtsson, H.
;
Harley, V.
;
Vilain, E.
;
Sinclair, A.
;
et al.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
Discover
Author
2
et al.
2
Eyre, H.
2
Kortschak, R.
2
Mulley, J.
1
Adelson, D.
1
Allen, K.
1
Andreas, J.
1
Arboleda, V.
1
Bagrodia, S.
1
Bengtsson, H.
.
next >
Subject
6
Female
4
Mice
3
Disease Models, Animal
3
Molecular Sequence Data
3
Pedigree
2
Base Sequence
2
Chromosome Mapping
2
Chromosomes, Human, Pair 19
2
Cloning, Molecular
2
DNA-Binding Proteins
.
next >
Date issued
6
2010 - 2019
3
1998 - 1999