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Results 1-10 of 16 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2019
GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon
Tingang Wonkam, E.
;
Chimusa, E.
;
Noubiap, J.J.
;
Adadey, S.M.
;
F Fokouo, J.V.
;
Wonkam, A.
2018
Chromosome structural anomalies due to aberrant spindle forces exerted at gene editing sites in meiosis
Łuksza, M.
;
Kanaan, J.
;
Marthiens, V.
;
Lane, S.
;
Jones, K.
;
Terret, M.
;
Basto, R.
;
Verlhac, M.
2017
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, M.
;
Heymann, G.
;
Wang, T.
;
Coe, B.
;
Turner, T.
;
Stessman, H.
;
Hoekzema, K.
;
Kvarnung, M.
;
Shaw, M.
;
Friend, K.
;
Liebelt, J.
;
Barnett, C.
;
Thompson, E.
;
Haan, E.
;
Guo, H.
;
Anderlid, B.
;
Nordgren, A.
;
Lindstrand, A.
;
Vandeweyer, G.
;
Alberti, A.
;
et al.
2018
ADCY9 genetic variants and cardiovascular outcomes with evacetrapib in patients with high-risk vascular disease: a nested case-control study
Nissen, S.
;
Pillai, S.
;
Nicholls, S.
;
Wolski, K.
;
Riesmeyer, J.
;
Weerakkody, G.
;
Foster, W.
;
McErlean, E.
;
Li, L.
;
Bhatnagar, P.
;
Ruotolo, G.
;
Lincoff, A.
2013
Influence of aromatase absence on the gene expression and histology of the mouse meibomian gland
Rahimi Darabad, R.
;
Suzuki, T.
;
Richards, S.
;
Jensen, R.
;
Jakobiec, F.
;
Zakka, F.
;
Liu, S.
;
Sullivan, D.
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.
2013
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders
Nguyen, L.
;
Kim, H.
;
Rosenfeld, J.
;
Shen, Y.
;
Gusella, J.
;
Lacassie, Y.
;
Layman, L.
;
Shaffer, L.
;
Gecz, J.
2011
Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations
Dibbens, L.
;
Kneen, R.
;
Bayly, M.
;
Heron, S.
;
Arsov, T.
;
Damiano, J.
;
Desai, T.
;
Gibbs, J.
;
McKenzie, F.
;
Mulley, J.
;
Ronan, A.
;
Scheffer, I.
Discover
Author
5
et al.
3
Coe, B.
3
Gecz, J.
3
Kvarnung, M.
2
Friend, K.
2
Hoekzema, K.
2
Liebelt, J.
2
Stessman, H.
2
Turner, T.
2
Wang, T.
.
next >
Subject
3
Mice
2
Autistic Disorder
2
Case-Control Studies
2
Child, Preschool
2
Cohort Studies
2
Developmental Disabilities
2
Disease Models, Animal
2
Epilepsy
2
Exome
2
Gene Expression Profiling
.
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