Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders (English)

in HUMAN MOLECULAR GENETICS ; 27 , 7 ; 1212-1227
HUMAN MOLECULAR GENETICS
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Table of contents – Volume 27, Issue 7

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Tables of content are generated automatically and are based on records of articles contained that are available in the TIB-Portal index. Due to missing records of articles, the volume display may be incomplete, even though the whole journal is available at TIB.

1123
Testicular MTHFR deficiency may explain sperm DNA hypomethylation associated with high dose folic acid supplementation
Aarabi, Mahmoud / Christensen, Karen E / Chan, Donovan / Leclerc, Daniel / Landry, Mylène / Ly, Lundi / Rozen, Rima / Trasler, Jacquetta | 2018
1136
CHEK1 coordinates DNA damage signaling and meiotic progression in the male germline of mice
Abe, Hironori / Alavattam, Kris G / Kato, Yasuko / Castrillon, Diego H / Pang, Qishen / Andreassen, Paul R / Namekawa, Satoshi H | 2018
1150
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2
Guo, Tingwei / Diacou, Alexander / Nomaru, Hiroko / McDonald-McGinn, Donna M / Hestand, Matthew / Demaerel, Wolfram / Zhang, Liangtian / Zhao, Yingjie / Ujueta, Francisco / Shan, Jidong et al. | 2018
1164
From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria
Lenglet, Hugo / Schmitt, Caroline / Grange, Thomas / Manceau, Hana / Karboul, Narjesse / Bouchet-Crivat, Florian / Robreau, Anne-Marie / Nicolas, Gael / Lamoril, Jerôme / Simonin, Sylvie et al. | 2018
1174
Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stage
Sudo, A. / Kanagawa, M. / Kondo, M. / Ito, C. / Kobayashi, K. / Endo, M. / Minami, Y. / Aiba, A. / Toda, T. | 2018
1186
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies
Bartsakoulia, Marina / Pyle, Angela / Troncoso-Chandía, Diego / Vial-Brizzi, Josefa / Paz-Fiblas, Marysol V / Duff, Jennifer / Griffin, Helen / Boczonadi, Veronika / Lochmüller, Hanns / Kleinle, Stephanie et al. | 2018
1196
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia
Lorès, P. / Coutton, C. / El Khouri, E. / Stouvenel, L. / Givelet, M. l. / Thomas, L. / Rode, B. / Schmitt, A. / Louis, B. / Sakheli, Z. | 2018
1212
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders
Estruch, Sara B / Graham, Sarah A / Quevedo, Martí / Vino, Arianna / Dekkers, Dick H W / Deriziotis, Pelagia / Sollis, Elliot / Demmers, Jeroen / Poot, Raymond A / Fisher, Simon E | 2018
1228
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
Portnoi, M. F. / Dumargne, M. C. / Rojo, S. / Witchel, S. F. / Duncan, A. J. / Eozenou, C. / Bignon-Topalovic, J. / Yatsenko, S. A. / Rajkovic, A. / Reyes-Mugica, M. | 2018
1241
A tri-serine cluster within the topoisomerase IIα-interaction domain of the BLM helicase is required for regulating chromosome breakage in human cells
Behnfeldt, Julia Harris / Acharya, Samir / Tangeman, Larissa / Gocha, April Sandy / Keirsey, Jeremy / Groden, Joanna | 2018
1252
Human cis-acting elements regulating escape from X-chromosome inactivation function in mouse
Peeters, S. B. / Korecki, A. J. / Simpson, E. M. / Brown, C. J. | 2018
1263
Differentially expressed microRNAs in the aqueous humor of patients with exfoliation glaucoma or primary open-angle glaucoma
Drewry, Michelle D / Challa, Pratap / Kuchtey, John G / Navarro, Iris / Helwa, Inas / Hu, Yanzhong / Mu, Hongmei / Stamer, W Daniel / Kuchtey, Rachel W / Liu, Yutao | 2018
1276
Elongator subunit 3 (ELP3) modifies ALS through tRNA modification
Bento-Abreu, A. / Jager, G. / Swinnen, B. / Rué, L. / Hendrickx, S. / Jones, A. / Staats, K. A. / Taes, I. / Eykens, C. / Nonneman, A. | 2018
1290
Astrocytes: new players in progressive myoclonus epilepsy of Lafora type
Rubio-Villena, C. / Viana, R. / Bonet, J. / Garcia-Gimeno, M. A. / Casado, M. / Heredia, M. / Sanz, P. | 2018
1301
Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studies
Lawn, Rebecca B / Anderson, Emma L / Suderman, Matthew / Simpkin, Andrew J / Gaunt, Tom R / Teschendorff, Andrew E / Widschwendter, Martin / Hardy, Rebecca / Kuh, Diana / Relton, Caroline L et al. | 2018
1309
The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6
Sacristan-Reviriego, Almudena / Bellingham, James / Prodromou, Chrisostomos / Boehm, Annika N / Aichem, Annette / Kumaran, Neruban / Bainbridge, James / Michaelides, Michel / van der Spuy, Jacqueline | 2018
1310
A recurrent de novo missense mutation in UBTF causes developmental neuroregression
Toro, Camilo / Hori, Roderick T / Malicdan, May Christine V / Tifft, Cynthia J / Goldstein, Amy / Gahl, William A / Adams, David R / Fauni, Harper B / Wolfe, Lynne A / Xiao, Jianfeng et al. | 2018

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