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Assessment of Stx-1A gene polymorphism (rs1569061) in relation to the development of multiple sclerosis in Egyptian patients
Habib, Christine A, El-Sebai, Aziza A, Fouad, Mohamed M, El-Mohamdy, Marwa A, Abdel Ghani, Amani M, Bawady, Somia A
Published in The Egyptian journal of immunology (01.04.2024)
Published in The Egyptian journal of immunology (01.04.2024)
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Partial Sleep Restriction Activates Immune Response-Related Gene Expression Pathways: Experimental and Epidemiological Studies in Humans
Aho, Vilma, Ollila, Hanna M., Rantanen, Ville, Kronholm, Erkki, Surakka, Ida, van Leeuwen, Wessel M. A., Lehto, Maili, Matikainen, Sampsa, Ripatti, Samuli, Härmä, Mikko, Sallinen, Mikael, Salomaa, Veikko, Jauhiainen, Matti, Alenius, Harri, Paunio, Tiina, Porkka-Heiskanen, Tarja
Published in PloS one (23.10.2013)
Published in PloS one (23.10.2013)
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Differential expression of the regulated catecholamine secretory pathway in different hereditary forms of pheochromocytoma
Eisenhofer, Graeme, Huynh, Thanh-Truc, Elkahloun, Abdel, Morris, John C, Bratslavsky, Gennady, Linehan, W. Marston, Zhuang, Zhengping, Balgley, Brian M, Lee, Cheng S, Mannelli, Massimo, Lenders, Jacques W. M, Bornstein, Stefan R, Pacak, Karel
Published in American journal of physiology: endocrinology and metabolism (01.11.2008)
Published in American journal of physiology: endocrinology and metabolism (01.11.2008)
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Regulation of munc18-1 and syntaxin-1A interactive partners in schizophrenia prefrontal cortex: down-regulation of munc18-1a isoform and 75 kDa SNARE complex after antipsychotic treatment
Gil-Pisa, Itziar, Munarriz-Cuezva, Eva, Ramos-Miguel, Alfredo, Urigüen, Leyre, Meana, J. Javier, García-Sevilla, Jesús A.
Published in The international journal of neuropsychopharmacology (01.06.2012)
Published in The international journal of neuropsychopharmacology (01.06.2012)
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The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease
Guerini, Franca R., Ripamonti, Enrico, Costa, Andrea S., Zanzottera, Milena, Agliardi, Cristina, Bolognesi, Elisabetta, Clerici, Mario, Racca, Vittorio
Published in Medicine (Baltimore) (01.06.2019)
Published in Medicine (Baltimore) (01.06.2019)
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A syntaxin 1, Galpha(o), and N-type calcium channel complex at a presynaptic nerve terminal: analysis by quantitative immunocolocalization
Li, Qi, Lau, Anthony, Morris, Terence J., Guo, Lin, Fordyce, Christopher B., Stanley, Elise F.
Published in The Journal of neuroscience (21.04.2004)
Published in The Journal of neuroscience (21.04.2004)
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Negative Regulation of Syntaxin4/SNAP-23/VAMP2-Mediated Membrane Fusion by Munc18c In Vitro
Brandie, Fiona M., Aran, Veronica, Verma, Avani, McNew, James A., Bryant, Nia J., Gould, Gwyn W.
Published in PloS one (31.12.2008)
Published in PloS one (31.12.2008)
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Synaptic protein deficits are associated with dementia irrespective of extreme old age
Schnaider Beeri, Michal, Haroutunian, Vahram, Schmeidler, James, Sano, Mary, Fam, Peter, Kavanaugh, Aaron, Barr, Alasdair M., Honer, William G., Katsel, Pavel
Published in Neurobiology of aging (01.06.2012)
Published in Neurobiology of aging (01.06.2012)
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Loss of Munc18-1 long splice variant in GABAergic terminals is associated with cognitive decline and increased risk of dementia in a community sample
Ramos-Miguel, Alfredo, Hercher, Christa, Beasley, Clare L., Barr, Alasdair M., Bayer, Thomas A., Falkai, Peter, Leurgans, Sue E., Schneider, Julie A., Bennett, David A., Honer, William G.
Published in Molecular neurodegeneration (02.12.2015)
Published in Molecular neurodegeneration (02.12.2015)
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Identification of novel variants associated with warfarin stable dosage by use of a two‐stage extreme phenotype strategy
Luo, Z., Li, X., Zhu, M., Tang, J., Li, Z., Zhou, X., Song, G., Liu, Z., Zhou, H., Zhang, W.
Published in Journal of thrombosis and haemostasis (01.01.2017)
Published in Journal of thrombosis and haemostasis (01.01.2017)
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High prevalence of diabetes and pre-diabetes in adults with Williams syndrome
Pober, B.R., Wang, E., Caprio, S., Petersen, K.F., Brandt, C., Stanley, T., Osborne, L.R., Dzuria, J., Gulanski, B.
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.05.2010)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.05.2010)
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Tolerance to the anhedonic effects of lipopolysaccharide is associated with changes in syntaxin immunoreactivity in the nucleus accumbens
Barr, Alasdair M., Song, Cai, Sawada, Ken, Young, Clint E., Honer, William G., Phillips, Anthony G.
Published in The international journal of neuropsychopharmacology (01.03.2003)
Published in The international journal of neuropsychopharmacology (01.03.2003)
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Genetic variants of synaptic vesicle and presynaptic plasma membrane proteins in idiopathic generalized epilepsy
Yilmaz, Mustafa, Edgunlu, Tuba Gokdogan, Yilmaz, Nigar, Cetin, Esin Sakalli, Celik, Sevim Karakas, Emir, Gülser Karadaban, Sözen, Ayşe
Published in Journal of receptors and signal transduction (01.02.2014)
Published in Journal of receptors and signal transduction (01.02.2014)
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Aberrant localization of fusion receptors involved in regulated exocytosis in salivary glands of Sjögren’s syndrome patients is linked to ectopic mucin secretion
Barrera, María-José, Sánchez, Marianela, Aguilera, Sergio, Alliende, Cecilia, Bahamondes, Verónica, Molina, Claudio, Quest, Andrew F.G., Urzúa, Ulises, Castro, Isabel, González, Sergio, Sung, Hsiao Hsin, Albornoz, Amelina, Hermoso, Marcela, Leyton, Cecilia, González, María-Julieta
Published in Journal of autoimmunity (01.08.2012)
Published in Journal of autoimmunity (01.08.2012)
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Polymorphisms of ACMSD-TMEM163, MCCC1, and BCKDK-STX1B Are Not Associated with Parkinson’s Disease in Taiwan
Fung, Hon-Chung, Chen, Yi-Chun, Chen, Chiung-Mei, Chang, Kuo-Hsuan, Wu, Yih-Ru
Published in Parkinson's disease (01.01.2019)
Published in Parkinson's disease (01.01.2019)
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A novel STXBP1 mutation causes focal seizures with neonatal onset
Vatta, Matteo, Tennison, Michael B, Aylsworth, Arthur S, Turcott, Christie M, Guerra, Maria P, Eng, Christine M, Yang, Yaping
Published in Journal of child neurology (01.06.2012)
Published in Journal of child neurology (01.06.2012)
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