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Results 1-10 of 19 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2016
CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell follicles
Leong, Y.
;
Chen, Y.
;
Ong, H.
;
Wu, D.
;
Man, K.
;
Deleage, C.
;
Minnich, M.
;
Meckiff, B.
;
Wei, Y.
;
Hou, Z.
;
Zotos, D.
;
Fenix, K.
;
Atnerkar, A.
;
Preston, S.
;
Chipman, J.
;
Beilman, G.
;
Allison, C.
;
Sun, L.
;
Wang, P.
;
Xu, J.
;
et al.
2016
TBC1D24 genotype-phenotype correlation
Balestrini, S.
;
Milh, M.
;
Castiglioni, C.
;
Lüthy, K.
;
Finelli, M.
;
Verstreken, P.
;
Cardon, A.
;
Stražišar, B.
;
Holder, J.
;
Lesca, G.
;
Mancardi, M.
;
Poulat, A.
;
Repetto, G.
;
Banka, S.
;
Bilo, L.
;
Birkeland, L.
;
Bosch, F.
;
Brockmann, K.
;
Cross, J.
;
Doummar, D.
;
et al.
2016
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
Cohen, O.
;
Weickert, T.
;
Hess, J.
;
Paish, L.
;
McCoy, S.
;
Rothmond, D.
;
Galletly, C.
;
Liu, D.
;
Weinberg, D.
;
Huang, X.
;
Xu, Q.
;
Shen, Y.
;
Zhang, D.
;
Yue, W.
;
Yan, J.
;
Wang, L.
;
Lu, T.
;
He, L.
;
Shi, Y.
;
Xu, M.
;
et al.
2016
HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study
Friez, M.
;
Brooks, S.
;
Stevenson, R.
;
Field, M.
;
Basehore, M.
;
Adès, L.
;
Sebold, C.
;
Mcgee, S.
;
Saxon, S.
;
Skinner, C.
;
Craig, M.
;
Murray, L.
;
Simensen, R.
;
Yap, Y.
;
Shaw, M.
;
Gardner, A.
;
Corbett, M.
;
Kumar, R.
;
Bosshard, M.
;
Van Loon, B.
;
et al.
2016
Point mutations in Exon 1B of APC reveal gastric adenocarcinoma and proximal polyposis of the stomach as a familial adenomatous polyposis variant
Li, J.
;
Woods, S.
;
Healey, S.
;
Beesley, J.
;
Chen, X.
;
Lee, J.
;
Sivakumaran, H.
;
Wayte, N.
;
Nones, K.
;
Waterfall, J.
;
Pearson, J.
;
Patch, A.
;
Senz, J.
;
Ferreira, M.
;
Kaurah, P.
;
MacKenzie, R.
;
Heravi-Moussavi, A.
;
Hansford, S.
;
Lannagan, T.
;
Spurdle, A.
;
et al.
2016
Choline kinase alpha as an androgen receptor chaperone and prostate cancer therapeutic target
Asim, M.
;
Massie, C.
;
Orafidiya, F.
;
Pértega-Gomes, N.
;
Warren, A.
;
Esmaeili, M.
;
Selth, L.
;
Zecchini, H.
;
Luko, K.
;
Qureshi, A.
;
Baridi, A.
;
Menon, S.
;
Madhu, B.
;
Escriu, C.
;
Lyons, S.
;
Vowler, S.
;
Zecchini, V.
;
Shaw, G.
;
Hessenkemper, W.
;
Russell, R.
;
et al.
2016
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
Lewinsohn, M.
;
Brown, A.L.
;
Weinel, L.M.
;
Phung, C.
;
Rafidi, G.
;
Lee, M.K.
;
Schreiber, A.W.
;
Feng, J.
;
Babic, M.
;
Chong, C.E.
;
Lee, Y.
;
Yong, A.
;
Suthers, G.K.
;
Poplawski, N.
;
Altree, M.
;
Phillips, K.
;
Jaensch, L.
;
Fine, M.
;
D'Andrea, R.J.
;
Lewis, I.D.
;
et al.
2016
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
Hu, H.
;
Haas, S.
;
Chelly, J.
;
Van Esch, H.
;
Raynaud, M.
;
De Brouwer, A.
;
Weinert, S.
;
Froyen, G.
;
Frints, S.
;
Laumonnier, F.
;
Zemojtel, T.
;
Love, M.
;
Richard, H.
;
Emde, A.
;
Bienek, M.
;
Jensen, C.
;
Hambrock, M.
;
Fischer, U.
;
Langnick, C.
;
Feldkamp, M.
;
et al.
2016
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
van Bon, B.W.M.
;
Coe, B.P.
;
Bernier, R.
;
Green, C.
;
Gerdts, J.
;
Witherspoon, K.
;
Kleefstra, T.
;
Willemsen, M.H.
;
Kumar, R.
;
Bosco, P.
;
Fichera, M.
;
Li, D.
;
Amaral, D.
;
Cristofoli, F.
;
Peeters, H.
;
Haan, E.
;
Romano, C.
;
Mefford, H.C.
;
Scheffer, I.
;
Gecz, J.
;
et al.
2016
Multiplex families with epilepsy: success of clinical and molecular genetic characterization
Afawi, Z.
;
Oliver, K.L.
;
Kivity, S.
;
Mazarib, A.
;
Blatt, I.
;
Neufeld, M.Y.
;
Helbig, K.L.
;
Goldberg-Stern, H.
;
Misk, A.J.
;
Straussberg, R.
;
Walid, S.
;
Mahajnah, M.
;
Lerman-Sagie, T.
;
Ben-Zeev, B.
;
Kahana, E.
;
Masalha, R.
;
Kramer, U.
;
Ekstein, D.
;
Shorer, Z.
;
Wallace, R.H.
;
et al.
Discover
Author
2
Afawi, Z.
2
Brown, A.L.
2
Gecz, J.
2
Kumar, R.
2
Lewis, I.D.
2
Schwab, C.
1
Abdel-Wahab, M.
1
Adès, L.
1
Agwu, A.
1
Ahn, K.
.
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5
Genetic Predisposition to Disease
5
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4
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