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1. Sundberg M, Tochitsky I, Buchholz DE, Winden K, Kujala V, Kapur K, Cataltepe D, Turner D, Han MJ, Woolf CJ, Hatten ME, Sahin M   Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin   MOLECULAR PSYCHIATRY 2018 NOV; 23(11):2167-2183 Full Text | PMID/PMCID

2. Behesti H, Fore TR, Wu P, Horn Z, Leppert M, Hull C, Hatten ME   ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2018 OCT 9; 115(41):E9717-E9726 Full Text | PMID/PMCID

3. Horn Z, Behesti H, Hatten ME   N-cadherin provides a cis and trans ligand for astrotactin that functions in glial-guided neuronal migration   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 2018 OCT 16; 115(42):10556-10563 Full Text | PMID/PMCID

4. Jereb S, Hwang HW, Van Otterloo E, Govek EE, Fak JJ, Yuan Y, Hatten ME, Darnell RB   Differential 3 ' Processing of Specific Transcripts Expands Regulatory and Protein Diversity Across Neuronal Cell Types   ELIFE 2018 MAR 26; 7(?):? Article e34042 Full Text | PMID/PMCID

5. Leto K, Arancillo M, Becker EBE, Buffo A, Chiang C, Ding BJ, Dobyns WB, Dusart I, Haldipur P, Hatten ME, Hoshino M, Joyner AL, Kano M, Kilpatrick DL, Koibuchi N, Marino S, Martinez S, Millen KJ, Millner TO, Miyata T, Parmigiani E, Schilling K, Sekerkova G, Sillitoe RV, Sotelo C   Consensus Paper: Cerebellar Development   CEREBELLUM 2016 DEC; 15(6):789-828 Full Text | PMID/PMCID

6. Zhu XD, Girardo D, Govek EE, John K, Mellen M, Tamayo P, Mesirov JP, Hatten ME   Role of Tet1/3 Genes and Chromatin Remodeling Genes in Cerebellar Circuit Formation   NEURON 2016 JAN 6; 89(1):100-112 Full Text | PMID/PMCID

7. Maass PG, Aydin A, Luft FC, Schachterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Muhl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K   PDE3A mutations cause autosomal dominant hypertension with brachydactyly   NATURE GENETICS 2015 JUN; 47(6):647-653 Full Text | PMID/PMCID

8. Penas C, Govek EE, Fang Y, Ramachandran V, Daniel M, Wang WP, Maloof ME, Rahaim RJ, Bibian M, Kawauchi D, Finkelstein D, Han JL, Long J, Li B, Robbins DJ, Malumbres M, Roussel MF, Roush WR, Hatten ME, Ayad NG   Casein Kinase 1 delta Is an APC/C-Cdh1 Substrate that Regulates Cerebellar Granule Cell Neurogenesis   CELL REPORTS 2015 APR 14; 11(2):249-260 Full Text | PMID/PMCID

9. Hatten ME, Lisberger SG   Multitasking on the run   ELIFE 2013 MAR 19; 2(?):? Article e00641 Full Text | PMID/PMCID

10. Anne Sandrine L, Govek Eve-Ellen, Ayrault Olivier, Kim Jee Hae, Zhu Xiaodong, Murphy David A, Van Aelst Linda, Roussel Martine F, Hatten Mary E   WNT3 Inhibits Cerebellar Granule Neuron Progenitor Proliferation and Medulloblastoma Formation via MAPK Activation.   PloS one 2013 2013 Nov 26; 8(11):e81769-e81769 Full Text | PMID/PMCID

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