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Genes and Development, ISSN 0890-9369, 03/2008, Volume 22, Issue 6, pp. 756 - 769
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 05/2019, Volume 28, Issue 9, pp. 1487 - 1497
Abstract Zinc finger E-box-binding homeobox 2 (ZEB2) is a key developmental regulator of the central nervous system (CNS). Although the transcriptional... 
EPITHELIAL-MESENCHYMAL TRANSITION | SIP1 | MASH1 | TISSUE-SPECIFIC ENHANCERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | GENETICS & HEREDITY | GENERATION | DIFFERENTIATION | EXPRESSION | DLX1-AND-2 | VERTEBRATE | General
Journal Article
Journal Article
by Song, B and Lin, HX and Dong, LL and Ma, JJ and Jiang, ZG
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, ISSN 1128-3602, 03/2018, Volume 22, Issue 5, pp. 1290 - 1296
OBJECTIVE: Emerging evidence suggests aberrant microRNAs (miRNAs) expression is involved in cancer development through multiple. Although miR338 has shown to... 
SURVIVAL | Epithelial-mesenchymal transition | SIP1 | CARCINOGENESIS | DISEASE | Wnt/beta catenin | PHARMACOLOGY & PHARMACY | Gastric cancer | miR-338 | EXPRESSION | EphA2
Journal Article
Sleep Medicine, ISSN 1389-9457, 09/2019, Volume 61, pp. 44 - 51
Sleep disturbances are frequently reported in Mowat-Wilson Syndrome (MWS). The current study aimed to evaluate clinical and video-polysomnographic (VPSG)... 
Video-polysomnography | ESES | Mowat-wilson syndrome | Sleep disturbances | ELECTRICAL STATUS EPILEPTICUS | ZFHX1B SIP1 | DISTURBANCE | CLINICAL NEUROLOGY | CHILDREN | Sleep disorders | Sleep
Journal Article
by Zhao, W and Zhang, SC and Huang, WK and Li, X
CLINICAL AND EXPERIMENTAL MEDICINE, ISSN 1591-8890, 08/2018, Volume 18, Issue 3, pp. 445 - 451
Hirschsprung's disease (HSCR) is a common congenital malformation of the enteric nervous system. The pathophysiological basis remains unclear. Recently, the... 
Hirschsprung's disease | MEDICINE, RESEARCH & EXPERIMENTAL | SIP1 | ETIOLOGY | POLYMORPHISMS | MENTAL-RETARDATION | FORM | SIP1 gene | Point mutation | PCR-RFLP | CLINICAL-FEATURES | ZFHX1B | Immunohistochemistry | Genetic disorders | Codon | Gene mutations | Analysis | Genes | Genetic research | Birth defects | Genetic aspects | Nucleotide sequencing | Genetic polymorphisms | DNA sequencing
Journal Article
Journal Article
Sovremennye Tehnologii v Medicine, ISSN 2076-4243, 2018, Volume 10, Issue 2, pp. 20 - 28
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2013, Volume 110, Issue 8, pp. 2858 - 2863
Journal Article
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, ISSN 0960-894X, 03/2017, Volume 27, Issue 6, pp. 1371 - 1378
Previously published S1P receptor modulator benzyl ether derivatives have shown potential as being viable therapeutics for the treatment of neurodegenerative... 
CELLS | Sphingosine kinase | CHEMISTRY, MEDICINAL | Phosphoramidate | Benzyl ether derivative | CHEMISTRY, ORGANIC | SIP1 receptor agonist | FINGOLIMOD FTY720 | DISCOVERY | NUCLEOSIDE | Enzymatic processing | MULTIPLE-SCLEROSIS | PRODRUGS | SPHINGOSINE-1-PHOSPHATE | ProTide | TECHNOLOGY | PROTIDES
Journal Article
Brain Research, ISSN 0006-8993, 02/2019, Volume 1705, pp. 24 - 31
Zeb2 (Sip1, Zfhx1b) is a transcription factor that plays essential role in neuronal development. Sip1 mutation in humans was shown to cause Mowat-Wilson... 
Mowat-Wilson syndrome | Hippocampus | Brain development | Cortex | TRANSCRIPTION FACTORS | MENTAL-RETARDATION | CONDITIONAL KNOCKOUT | SMAD-INTERACTING PROTEIN-1 | CELL-FATE | NEUROSCIENCES | FATE DECISIONS | SIP1 | POSTMITOTIC NEURONS | HIRSCHSPRUNG-DISEASE | ZFHX1B | Neurons | Genetic transcription | Neurophysiology
Journal Article