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Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters. [electronic resource] by
- Grunseich, Christopher
- Wang, Isabel X
- Watts, Jason A
- Burdick, Joshua T
- Guber, Robert D
- Zhu, Zhengwei
- Bruzel, Alan
- Lanman, Tyler
- Chen, Kelian
- Schindler, Alice B
- Edwards, Nancy
- Ray-Chaudhury, Abhik
- Yao, Jianhua
- Lehky, Tanya
- Piszczek, Grzegorz
- Crain, Barbara
- Fischbeck, Kenneth H
- Cheung, Vivian G
Producer: 20190107
In:
Molecular cell vol. 69
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304.
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An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2. [electronic resource] by
- Mancini, Cecilia
- Orsi, Laura
- Guo, Yiran
- Li, Jiankang
- Chen, Yulan
- Wang, Fengxiang
- Tian, Lifeng
- Liu, Xuanzhu
- Zhang, Jianguo
- Jiang, Hui
- Nmezi, Bruce Shike
- Tatsuta, Takashi
- Giorgio, Elisa
- Di Gregorio, Eleonora
- Cavalieri, Simona
- Pozzi, Elisa
- Mortara, Paolo
- Caglio, Maria Marcella
- Balducci, Alessandro
- Pinessi, Lorenzo
- Langer, Thomas
- Padiath, Quasar S
- Hakonarson, Hakon
- Zhang, Xiuqing
- Brusco, Alfredo
Producer: 20150630
In:
BMC medical genetics vol. 16
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306.
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SMN and symmetric arginine dimethylation of RNA polymerase II C-terminal domain control termination. [electronic resource] by
- Zhao, Dorothy Yanling
- Gish, Gerald
- Braunschweig, Ulrich
- Li, Yue
- Ni, Zuyao
- Schmitges, Frank W
- Zhong, Guoqing
- Liu, Ke
- Li, Weiguo
- Moffat, Jason
- Vedadi, Masoud
- Min, Jinrong
- Pawson, Tony J
- Blencowe, Benjamin J
- Greenblatt, Jack F
Producer: 20160125
In:
Nature vol. 529
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307.
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308.
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Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients. [electronic resource] by
- Tazir, M
- Ali-Pacha, L
- M'Zahem, A
- Delaunoy, J P
- Fritsch, M
- Nouioua, S
- Benhassine, T
- Assami, S
- Grid, D
- Vallat, J M
- Hamri, A
- Koenig, M
Producer: 20090504
In:
Journal of the neurological sciences vol. 278
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309.
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Genetic predisposition and environmental danger signals initiate chronic autoimmune hepatitis driven by CD4+ T cells. [electronic resource] by
- Hardtke-Wolenski, Matthias
- Fischer, Katja
- Noyan, Fatih
- Schlue, Jerome
- Falk, Christine S
- Stahlhut, Maike
- Woller, Norman
- Kuehnel, Florian
- Taubert, Richard
- Manns, Michael P
- Jaeckel, Elmar
Producer: 20140116
In:
Hepatology (Baltimore, Md.) vol. 58
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310.
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Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2. [electronic resource] by
- MacKay, Craig
- Déclais, Anne-Cécile
- Lundin, Cecilia
- Agostinho, Ana
- Deans, Andrew J
- MacArtney, Thomas J
- Hofmann, Kay
- Gartner, Anton
- West, Stephen C
- Helleday, Thomas
- Lilley, David M J
- Rouse, John
Producer: 20100802
In:
Cell vol. 142
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311.
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Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair. [electronic resource] by
- Seguí, Nuria
- Mina, Leonardo B
- Lázaro, Conxi
- Sanz-Pamplona, Rebeca
- Pons, Tirso
- Navarro, Matilde
- Bellido, Fernando
- López-Doriga, Adriana
- Valdés-Mas, Rafael
- Pineda, Marta
- Guinó, Elisabet
- Vidal, August
- Soto, José Luís
- Caldés, Trinidad
- Durán, Mercedes
- Urioste, Miguel
- Rueda, Daniel
- Brunet, Joan
- Balbín, Milagros
- Blay, Pilar
- Iglesias, Silvia
- Garré, Pilar
- Lastra, Enrique
- Sánchez-Heras, Ana Beatriz
- Valencia, Alfonso
- Moreno, Victor
- Pujana, Miguel Ángel
- Villanueva, Alberto
- Blanco, Ignacio
- Capellá, Gabriel
- Surrallés, Jordi
- Puente, Xose S
- Valle, Laura
Producer: 20151109
In:
Gastroenterology vol. 149
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312.
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A missense variant in FTCD is associated with arsenic metabolism and toxicity phenotypes in Bangladesh. [electronic resource] by
- Pierce, Brandon L
- Tong, Lin
- Dean, Samantha
- Argos, Maria
- Jasmine, Farzana
- Rakibuz-Zaman, Muhammad
- Sarwar, Golam
- Islam, Md Tariqul
- Shahriar, Hasan
- Islam, Tariqul
- Rahman, Mahfuzar
- Yunus, Md
- Lynch, Vincent J
- Oglesbee, Devin
- Graziano, Joseph H
- Kibriya, Muhammad G
- Gamble, Mary V
- Ahsan, Habibul
Producer: 20190429
In:
PLoS genetics vol. 15
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313.
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Oxidized phospholipids regulate amino acid metabolism through MTHFD2 to facilitate nucleotide release in endothelial cells. [electronic resource] by
- Hitzel, Juliane
- Lee, Eunjee
- Zhang, Yi
- Bibli, Sofia Iris
- Li, Xiaogang
- Zukunft, Sven
- Pflüger, Beatrice
- Hu, Jiong
- Schürmann, Christoph
- Vasconez, Andrea Estefania
- Oo, James A
- Kratzer, Adelheid
- Kumar, Sandeep
- Rezende, Flávia
- Josipovic, Ivana
- Thomas, Dominique
- Giral, Hector
- Schreiber, Yannick
- Geisslinger, Gerd
- Fork, Christian
- Yang, Xia
- Sigala, Fragiska
- Romanoski, Casey E
- Kroll, Jens
- Jo, Hanjoong
- Landmesser, Ulf
- Lusis, Aldons J
- Namgaladze, Dmitry
- Fleming, Ingrid
- Leisegang, Matthias S
- Zhu, Jun
- Brandes, Ralf P
Producer: 20181226
In:
Nature communications vol. 9
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316.
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317.
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Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy. [electronic resource] by
- Duquette, Antoine
- Roddier, Katel
- McNabb-Baltar, Julia
- Gosselin, Isabelle
- St-Denis, Anik
- Dicaire, Marie-Josée
- Loisel, Lina
- Labuda, Damian
- Marchand, Luc
- Mathieu, Jean
- Bouchard, Jean-Pierre
- Brais, Bernard
Producer: 20050425
In:
Annals of neurology vol. 57
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