Folia Biologica
Journal of Cellular and Molecular Biology, Charles University 

Crossref Cited-by Linking

• Kim Jeongah, Park Si-Hyung, Sun Woong: The Differential Developmental Neurotoxicity of Valproic Acid on Anterior and Posterior Neural Induction of Human Pluripotent Stem Cells. Int J Stem Cells 2025, 18, 49. <https://doi.org/10.15283/ijsc24066>
• Cergel Eda, Tuzuner Burcin Alev, Turkyilmaz Ismet Burcu, Oktay Sehkar, Magaji Umar Faruk, Sacan Ozlem, Yanardag Refiye, Yarat Aysen: Reversal of Valproate\u2010Induced Major Salivary Gland Changes By Moringa Oleifera Extract in Rats. Chemistry & Biodiversity 2024, 21. <https://doi.org/10.1002/cbdv.202301959>
• Elik Gülsüm, Oktay Sehkar, Turkyilmaz Ismet Burcu, Alev-Tuzuner Burcin, Magaji Umar Faruk, Sacan Ozlem, Yanardag Refiye, Yarat Aysen: Dermatoprotective effect of Moringa oleifera leaf extract on sodium valproate-induced skin damage in rats. Drug and Chemical Toxicology 2024, 47, 1257. <https://doi.org/10.1080/01480545.2024.2369586>
• Abu Shamma Amani, Abu Ali Hijazi, Kamel Shayma: Synthesis, characterization and biological properties of mixed ligand complexes of cobalt(II/III) valproate with 2,9\u2010dimethyl\u20101,10\u2010phenanthroline and 1,10\u2010phenanthroline. Applied Organom Chemis 2018, 32. <https://doi.org/10.1002/aoc.3904>
• Barneh Farnaz, Salimi Mona, Goshadrou Fatemeh, Ashtiani Minoo, Mirzaie Mehdi, Zali Hakimeh, Jafari Mohieddin: Valproic acid inhibits the protective effects of stromal cells against chemotherapy in breast cancer: Insights from proteomics and systems biology. J of Cellular Biochemistry 2018, 119, 9270. <https://doi.org/10.1002/jcb.27196>
• Rabadiya Samir, Bhadada Shradhha, Dudhrejiya Ashvin, Vaishnav Devendra, Patel Bhoomika: Magnesium valproate ameliorates type 1 diabetes and cardiomyopathy in diabetic rats through estrogen receptors. Biomedicine & Pharmacotherapy 2018, 97, 919. <https://doi.org/10.1016/j.biopha.2017.10.137>
• Leu Sy\u2010Jye, Yang Yi\u2010Yuan, Liu Hsing\u2010Cheng, Cheng Chieh\u2010Yu, Wu Yu\u2010Chen, Huang Ming\u2010Chyi, Lee Yuen\u2010Lun, Chen Chi\u2010Ching, Shen Winston W., Liu Ko\u2010Jiunn: Valproic Acid and Lithium Meditate Anti\u2010Inflammatory Effects by Differentially Modulating Dendritic Cell Differentiation and Function. Journal Cellular Physiology 2017, 232, 1176. <https://doi.org/10.1002/jcp.25604>
• Um Soyoun, Lee Ho, Zhang Qingbin, Kim Hui Young, Lee Joo-Hee, Seo Byoung Moo: Valproic Acid Modulates the Multipotency in Periodontal Ligament Stem Cells via p53-Mediated Cell Cycle. Tissue Eng Regen Med 2017, 14, 153. <https://doi.org/10.1007/s13770-017-0027-4>
• Sargolzaei Javad, Rabbani-Chadegani Azra, Mollaei Hossein, Deezagi Abdolkhalegh: Spectroscopic analysis of the interaction of valproic acid with histone H1 in solution and in chromatin structure. International Journal of Biological Macromolecules 2017, 99, 427. <https://doi.org/10.1016/j.ijbiomac.2017.02.098>
• Abu Ali Hijazi, Abu Shamma Amani, Kamel Shayma: New mixed ligand cobalt(II/III) complexes based on the drug sodium valproate and bioactive nitrogen-donor ligands. Synthesis, structure and biological properties. Journal of Molecular Structure 2017, 1142, 40. <https://doi.org/10.1016/j.molstruc.2017.04.048>
• Zhang Y., Wu J.Y., Weng L.H., Li X.X., Yu L.J., Xu Y.: Valproic acid protects against MPP+-mediated neurotoxicity in SH-SY5Y Cells through autophagy. Neuroscience Letters 2017, 638, 60. <https://doi.org/10.1016/j.neulet.2016.12.017>
• Flores-Ramos Mónica, Leff Philippe, Fernández-Guasti Alonso, Becerra Palars Claudia: Is it important to consider the sex of the patient when using lithium or valproate to treat the bipolar disorder?. Pharmacology Biochemistry and Behavior 2017, 152, 105. <https://doi.org/10.1016/j.pbb.2016.02.003>
• Vishwakarma Sandeep Kumar, Bardia Avinash, Chandrakala L., Arshiya Sana, Paspala Syed Ameer Basha, Satti Vishnupriya, Khan Aleem Ahmed: Enhanced neuroprotective effect of mild-hypothermia with VPA against ethanol\u2013mediated neuronal injury. Tissue and Cell 2017, 49, 638. <https://doi.org/10.1016/j.tice.2017.09.004>
• Zhang Hailong, Zhang Wei, Zhou Yong, Jiang Yuhua, Li Shupeng: Dual Functional Mesoporous Silicon Nanoparticles Enhance the Radiosensitivity of VPA in Glioblastoma. Translational Oncology 2017, 10, 229. <https://doi.org/10.1016/j.tranon.2016.12.011>
• Hawkins Kate E., Moschidou Dafni, Faccenda Danilo, Wruck Wasco, Martin-Trujillo Alex, Hau Kwan-Leong, Ranzoni Anna Maria, Sanchez-Freire Veronica, Tommasini Fabio, Eaton Simon, De Coppi Paolo, Monk David, Campanella Michelangelo, Thrasher Adrian J., Adjaye James, Guillot Pascale V.: Human Amniocytes Are Receptive to Chemically Induced Reprogramming to Pluripotency. Molecular Therapy 2017, 25, 427. <https://doi.org/10.1016/j.ymthe.2016.11.014>
• Venosa Alessandro, Gow James G., Hall LeRoy, Malaviya Rama, Gow Andrew J., Laskin Jeffrey D., Laskin Debra L.: Regulation of Nitrogen Mustard-Induced Lung Macrophage Activation by Valproic Acid, a Histone Deacetylase Inhibitor. Toxicological Sciences 2017, 157, 222. <https://doi.org/10.1093/toxsci/kfx032>
• Bertelsen Freja, Folloni Davide, Møller Arne, Landau Anne M., Scheel-Krüger Jørgen, Winterdahl Michael: Suppressed play behaviour and decreased oxytocin receptor binding in the amygdala after prenatal exposure to low-dose valproic acid. Behavioural Pharmacology 2017, 28, 450. <https://doi.org/10.1097/FBP.0000000000000316>
• Ishida Ryo, Koyanagi-Aoi Michiyo, Oshima Nobu, Kakeji Yoshihiro, Aoi Takashi: The Tissue-Reconstructing Ability of Colon CSCs Is Enhanced by FK506 and Suppressed by GSK3 Inhibition. Molecular Cancer Research 2017, 15, 1455. <https://doi.org/10.1158/1541-7786.MCR-17-0071>
• Kim Ki Chan, Choi Chang Soon, Gonzales Edson Luck T., Mabunga Darine Froy N., Lee Sung Hoon, Jeon Se Jin, Hwangbo Ram, Hong Minha, Ryu Jong Hoon, Han Seol-Heui, Bahn Geon Ho, Shin Chan Young: Valproic Acid Induces Telomerase Reverse Transcriptase Expression during Cortical Development. Exp Neurobiol 2017, 26, 252. <https://doi.org/10.5607/en.2017.26.5.252>
• Khan Sabbir, Jena Gopabandhu: Valproic Acid Improves Glucose Homeostasis by Increasing Beta-Cell Proliferation, Function, and Reducing its Apoptosis through HDAC Inhibition in Juvenile Diabetic Rat. J Biochem Mol Toxicol 2016, 30, 438. <https://doi.org/10.1002/jbt.21807>
• Welbat Jariya Umka, Chaisawang Pornthip, Chaijaroonkhanarak Wunnee, Prachaney Parichat, Pannangrong Wanassanun, Sripanidkulchai Bungorn, Wigmore Peter: Kaempferia parviflora extract ameliorates the cognitive impairments and the reduction in cell proliferation induced by valproic acid treatment in rats. Annals of Anatomy - Anatomischer Anzeiger 2016, 206, 7. <https://doi.org/10.1016/j.aanat.2016.04.029>
• Hardin Heather, Yu Xiao-Min, Harrison April D., Larrain Carolina, Zhang Ranran, Chen Jidong, Chen Herbert, Lloyd Ricardo V.: Generation of Novel Thyroid Cancer Stem-Like Cell Clones. The American Journal of Pathology 2016, 186, 1662. <https://doi.org/10.1016/j.ajpath.2016.02.003>
• Khan Sabbir, Kumar Sandeep, Jena Gopabandhu: Valproic acid reduces insulin-resistance, fat deposition and FOXO1-mediated gluconeogenesis in type-2 diabetic rat. Biochimie 2016, 125, 42. <https://doi.org/10.1016/j.biochi.2016.02.014>
• Guillot Pascale V.: Induced pluripotent stem (iPS) cells from human fetal stem cells. Best Practice & Research Clinical Obstetrics & Gynaecology 2016, 31, 112. <https://doi.org/10.1016/j.bpobgyn.2015.08.007>
• Woods Jared K., Rogina Blanka: The effects of Rpd3 on fly metabolism, health, and longevity. Experimental Gerontology 2016, 86, 124. <https://doi.org/10.1016/j.exger.2016.02.015>
• Jin Haibin, Guo Xiaoming: Valproic acid ameliorates coxsackievirus-B3-induced viral myocarditis by modulating Th17/Treg imbalance. Virol J 2016, 13. <https://doi.org/10.1186/s12985-016-0626-z>
• Sun Lichun, Qian Qingqing, Sun Guangchun, Mackey L. Vienna, Fuselier Joseph A., Coy David H., Yu Cui-Yun: Valproic acid induces NET cell growth arrest and enhances tumor suppression of the receptor-targeted peptide\u2013drug conjugate via activating somatostatin receptor type II. Journal of Drug Targeting 2016, 24, 169. <https://doi.org/10.3109/1061186X.2015.1066794>
• FENG SHUYU, YANG YUE, LV JINGYI, SUN LICHUN, LIU MINGQIU: Valproic acid exhibits different cell growth arrest effect in three HPV-positive/negative cervical cancer cells and possibly via inducing Notch1 cleavage and E6 downregulation. International Journal of Oncology 2016, 49, 422. <https://doi.org/10.3892/ijo.2016.3508>
• Khan Sabbir, Jena Gopabandhu, Tikoo Kulbhushan, Kumar Vinod: Valproate attenuates the proteinuria, podocyte and renal injury by facilitating autophagy and inactivation of NF-\u03baB/iNOS signaling in diabetic rat. Biochimie 2015, 110, 1. <https://doi.org/10.1016/j.biochi.2014.12.015>
• Balasubramanian Diana, Deng Alicia X., Doudney Kit, Hampton Mark B., Kennedy Martin A.: Valproic acid exposure leads to upregulation and increased promoter histone acetylation of sepiapterin reductase in a serotonergic cell line. Neuropharmacology 2015, 99, 79. <https://doi.org/10.1016/j.neuropharm.2015.06.018>
• Juliandi Berry, Tanemura Kentaro, Igarashi Katsuhide, Tominaga Takashi, Furukawa Yusuke, Otsuka Maky, Moriyama Noriko, Ikegami Daigo, Abematsu Masahiko, Sanosaka Tsukasa, Tsujimura Keita, Narita Minoru, Kanno Jun, Nakashima Kinichi: Reduced Adult Hippocampal Neurogenesis and Cognitive Impairments following Prenatal Treatment of the Antiepileptic Drug Valproic Acid. Stem Cell Reports 2015, 5, 996. <https://doi.org/10.1016/j.stemcr.2015.10.012>
• Ximenes José Christian Machado, Neves Kelly Rose Tavares, Leal Luzia Kalyne A. M., do Carmo Marta Regina Santos, Brito Gerly Anne de Castro, Naffah-Mazzacoratti Maria da Graça, Cavalheiro Ésper Abrão, Viana Glauce Socorro de Barros: Valproic Acid Neuroprotection in the 6-OHDA Model of Parkinson\u2019s Disease Is Possibly Related to Its Anti-Inflammatory and HDAC Inhibitory Properties. Journal of Neurodegenerative Diseases 2015, 2015, 1. <https://doi.org/10.1155/2015/313702>
• Chu Tianci, Zhou Hengxing, Lu Lu, Kong Xiaohong, Wang Tianyi, Pan Bin, Feng Shiqing: Valproic Acid-Mediated Neuroprotection and Neurogenesis After Spinal Cord Injury: From Mechanism to Clinical Potential. Regen. Med. 2015, 10, 193. <https://doi.org/10.2217/rme.14.86>
• Long Jun, Chang Li, Shen Yan, Gao Wen-Hui, Wu Yue-Nv, Dou Han-Bo, Huang Meng-Meng, Wang Ying, Fang Wei-Yue, Shan Jie-Hui, Wang Yue-Ying, Zhu Jiang, Chen Zhu, Hu Jiong: Valproic Acid Ameliorates Graft-versus-Host Disease by Downregulating Th1 and Th17 Cells. The Journal of Immunology 2015, 195, 1849. <https://doi.org/10.4049/jimmunol.1500578>
• ABAZA MOHAMED-SALAH I., BAHMAN ABDUL-MAJEED, AL-ATTIYAH RAJA\u2019A J.: Valproic acid, an anti-epileptic drug and a histone deacetylase inhibitor, in combination with proteasome inhibitors exerts antiproliferative, pro-apoptotic and chemosensitizing effects in human colorectal cancer cells: Underlying molecular mechanisms. International Journal of Molecular Medicine 2014, 34, 513. <https://doi.org/10.3892/ijmm.2014.1795>
• Bitman Michal, Vrzal Radim, Dvorak Zdenek, Pavek Petr: Valproate activates ERK signaling pathway in primary human hepatocytes. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2014, 158, 039. <https://doi.org/10.5507/bp.2012.038>
• Kim Youn-Jung, Lee Jina, Song Mi-Kyung, Han Taejun, Ryu Jae-Chun: Valproic acid inhibits cell size and cell proliferation by AMPK-mediated mTOR signaling pathway in JEG-3 cells. BioChip J 2013, 7, 267. <https://doi.org/10.1007/s13206-013-7310-9>
• Stempin Sandra, Andres Susanne, Bumke Scheer Maja, Rode Ariane, Nau Heinz, Seidel Albrecht, Lampen Alfonso: Valproic acid and its derivatives enhanced estrogenic activity but not androgenic activity in a structure dependent manner. Reproductive Toxicology 2013, 42, 49. <https://doi.org/10.1016/j.reprotox.2013.07.019>
• Chiu Chi-Tso, Wang Zhifei, Hunsberger Joshua G., Chuang De-Maw: Therapeutic Potential of Mood Stabilizers Lithium and Valproic Acid: Beyond Bipolar Disorder. Pharmacological Reviews 2013, 65, 105. <https://doi.org/10.1124/pr.111.005512>
• Mallela Mural, Hrubec Theresa: Reduction in Valproic Acid\u2013Induced Neural Tube Defects by Maternal Immune Stimulation: Role of Apoptosis. Birth Defects Research Pt B 2012, 95, 296. <https://doi.org/10.1002/bdrb.21018>
• Van Nifterik Krista A., Van den Berg Jaap, Slotman Ben J., Lafleur M. Vincent M., Sminia Peter, Stalpers Lukas J. A.: Valproic acid sensitizes human glioma cells for temozolomide and \u03b3-radiation. J Neurooncol 2012, 107, 61. <https://doi.org/10.1007/s11060-011-0725-z>
• Kwieci\u0144ska Patrycja, Taubøll Erik, Gregoraszczuk Ewa \u0141ucja: Comparison of the effects of valproic acid and levetiracetam on apoptosis in the human ovarian cancer cell line OVCAR-3. Pharmacological Reports 2012, 64, 603. <https://doi.org/10.1016/S1734-1140(12)70856-3>
• Rossetti Franco, de Araujo Furtado Marcio, Pak Thomas, Bailey Keenan, Shields Mallory, Chanda Soma, Addis Michael, Robertson Benjamin D., Moffett Mark, Lumley Lucille A., Yourick Debra L.: Combined diazepam and HDAC inhibitor treatment protects against seizures and neuronal damage caused by soman exposure. NeuroToxicology 2012, 33, 500. <https://doi.org/10.1016/j.neuro.2012.02.010>
• Cowden John, Padnos Beth, Hunter Deborah, MacPhail Robert, Jensen Karl, Padilla Stephanie: Developmental exposure to valproate and ethanol alters locomotor activity and retino-tectal projection area in zebrafish embryos. Reproductive Toxicology 2012, 33, 165. <https://doi.org/10.1016/j.reprotox.2011.11.111>
• Dell'Aversana Carmela, Lepore Ilaria, Altucci Lucia: HDAC modulation and cell death in the clinic. Experimental Cell Research 2012, 318, 1229. <https://doi.org/10.1016/j.yexcr.2012.01.025>
• Forthun Rakel Brendsdal, SenGupta Tanima, Skjeldam Hanne Kim, Lindvall Jessica Margareta, McCormack Emmet, Gjertsen Bjørn Tore, Nilsen Hilde, Moura Ivan Cruz: Cross-Species Functional Genomic Analysis Identifies Resistance Genes of the Histone Deacetylase Inhibitor Valproic Acid. PLoS ONE 2012, 7, e48992. <https://doi.org/10.1371/journal.pone.0048992>
• Gillet Nicolas, Vandermeers Fabian, De Brogniez Alix, Florins Arnaud, Nigro Annamaria, François Carole, Bouzar Amel-Baya, Verlaeten Olivier, Stern Eric, Lambert Didier M., Wouters Johan, Willems Luc: Chemoresistance to Valproate Treatment of Bovine Leukemia Virus-Infected Sheep; Identification of Improved HDAC Inhibitors. Pathogens 2012, 1, 65. <https://doi.org/10.3390/pathogens1020065>
• Wittenburg Luke A., Bisson Liam, Rose Barbara J., Korch Christopher, Thamm Douglas H.: The histone deacetylase inhibitor valproic acid sensitizes human and canine osteosarcoma to doxorubicin. Cancer Chemother Pharmacol 2011, 67, 83. <https://doi.org/10.1007/s00280-010-1287-z>
• Khan Sabbir, Ahmad Tauseef, Parekh Chintan Vishnubhai, Trivedi Priyanka Pushkarbhai, Kushwaha Sapana, Jena Gopabandhu: Investigation on sodium valproate induced germ cell damage, oxidative stress and genotoxicity in male Swiss mice. Reproductive Toxicology 2011, 32, 385. <https://doi.org/10.1016/j.reprotox.2011.09.007>
• Gotfryd Kamil, Hansen Maria, Kawa Anna, Ellerbeck Ursula, Nau Heinz, Berezin Vladimir, Bock Elisabeth, Walmod Peter S.: The Teratogenic Potencies of Valproic Acid Derivatives and Their Effects on Biological End\u2010points are Related to Changes in Histone Deacetylase and Erk1/2 Activities. Basic Clin Pharma Tox 2011, 109, 164. <https://doi.org/10.1111/j.1742-7843.2011.00702.x>
• Wu Jason Boyang, Shih Jean C.: Valproic Acid Induces Monoamine Oxidase A via Akt/Forkhead Box O1 Activation. Molecular Pharmacology 2011, 80, 714. <https://doi.org/10.1124/mol.111.072744>
• Go Hyo Sang, Seo Jung Eun, Kim Ki Chan, Han So Min, Kim Pitna, Kang Young Sun, Han Seol Heui, Shin Chan Young, Ko Kwang Ho: Valproic acid inhibits neural progenitor cell death by activation of NF-\u03baB signaling pathway and up-regulation of Bcl-XL. J Biomed Sci 2011, 18. <https://doi.org/10.1186/1423-0127-18-48>
• Haerian Batoul Sadat, Lim Kheng Seang, Tan Chong Tin, Raymond Azman Ali, Mohamed Zahurin: Association of ABCB1 Gene Polymorphisms and Their Haplotypes with Response to Antiepileptic Drugs: a Systematic Review and Meta-Analysis. Pharmacogenomics 2011, 12, 713. <https://doi.org/10.2217/pgs.10.212>
• Jentink Janneke, Bakker Marian K., Nijenhuis Cynthia M., Wilffert Bob, de Jong-van den Berg Lolkje T.W.: Does folic acid use decrease the risk for spina bifida after in utero exposure to valproic acid?. Pharmacoepidem. Drug Safe. 2010, 19, 803. <https://doi.org/10.1002/pds.1975>
• Nuutinen Tapio, Suuronen Tiina, Kauppinen Anu, Salminen Antero: Valproic acid stimulates clusterin expression in human astrocytes: Implications for Alzheimer's disease. Neuroscience Letters 2010, 475, 64. <https://doi.org/10.1016/j.neulet.2010.03.041>
• Umka J., Mustafa S., ElBeltagy M., Thorpe A., Latif L., Bennett G., Wigmore P.M.: Valproic acid reduces spatial working memory and cell proliferation in the hippocampus. Neuroscience 2010, 166, 15. <https://doi.org/10.1016/j.neuroscience.2009.11.073>
• Zhang Z.Y., Zhang Z., Schluesener H.J.: MS-275, an histone deacetylase inhibitor, reduces the inflammatory reaction in rat experimental autoimmune neuritis. Neuroscience 2010, 169, 370. <https://doi.org/10.1016/j.neuroscience.2010.04.074>
• ADAB NAGHME, O'DONOGHUE MICHAEL F: ANTI-EPILEPTIC DRUGS AND BRAIN AND BEHAVIOURAL DEVELOPMENT IN ANIMAL MODELS AND HUMANS. Fet. Matern. Med. Rev. 2010, 21, 283. <https://doi.org/10.1017/S0965539510000100>
• Gotfryd Kamil, Skladchikova Galina, Lepekhin Eugene A, Berezin Vladimir, Bock Elisabeth, Walmod Peter S: Cell type-specific anti-cancer properties of valproic acid: independent effects on HDAC activity and Erk1/2 phosphorylation. BMC Cancer 2010, 10. <https://doi.org/10.1186/1471-2407-10-383>
• Erlich Rafael B., Rickwood Danny, Coman William B., Saunders Nicholas A., Guminski Alexander: Valproic acid as a therapeutic agent for head and neck squamous cell carcinomas. Cancer Chemother Pharmacol 2009, 63, 381. <https://doi.org/10.1007/s00280-008-0747-1>
• Cournoyer Philippe, Desrosiers Richard R.: Valproic acid enhances protein l-isoaspartyl methyltransferase expression by stimulating extracellular signal-regulated kinase signaling pathway. Neuropharmacology 2009, 56, 839. <https://doi.org/10.1016/j.neuropharm.2009.01.008>
• Zádori Dénes, Geisz Andrea, Vámos Enik\u0151, Vécsei László, Klivényi Péter: Valproate ameliorates the survival and the motor performance in a transgenic mouse model of Huntington's disease. Pharmacology Biochemistry and Behavior 2009, 94, 148. <https://doi.org/10.1016/j.pbb.2009.08.001>
• Erhart S, Amann A, Haberlandt E, Edlinger G, Schmid A, Filipiak W, Schwarz K, Mochalski P, Rostasy K, Karall D, Scholl-Bürgi S: 3-Heptanone as a potential new marker for valproic acid therapy. J. Breath Res. 2009, 3, 016004. <https://doi.org/10.1088/1752-7155/3/1/016004>
• Bouzar Amel Baya, Boxus Mathieu, Defoiche Julien, Berchem Guy, Macallan Derek, Pettengell Ruth, Willis Fenella, Burny Arsène, Lagneaux Laurence, Bron Dominique, Chatelain Bernard, Chatelain Christian, Willems Luc: Valproate synergizes with purine nucleoside analogues to induce apoptosis of B\u2010chronic lymphocytic leukaemia cells. Br J Haematol 2009, 144, 41. <https://doi.org/10.1111/j.1365-2141.2008.07426.x>
• Floris Giuseppe, Debiec-Rychter Maria, Sciot Raf, Stefan Cristiana, Fieuws Steffen, Machiels Kathleen, Atadja Peter, Wozniak Agnieszka, Faa Gavino, Scho\u0308ffski Patrick: High Efficacy of Panobinostat Towards Human Gastrointestinal Stromal Tumors in a Xenograft Mouse Model. Clinical Cancer Research 2009, 15, 4066. <https://doi.org/10.1158/1078-0432.CCR-08-2588>
• Smith Jacqueline, Whitehall John: Sodium Valproate and the Fetus: A Case Study and Review of the Literature. Neonatal Network 2009, 28, 363. <https://doi.org/10.1891/0730-0832.28.6.363>
• Fischer Wiebke, Praetor Katrin, Metzner Linda, Neubert Reinhard H.H., Brandsch Matthias: Transport of valproate at intestinal epithelial (Caco-2) and brain endothelial (RBE4) cells: Mechanism and substrate specificity. European Journal of Pharmaceutics and Biopharmaceutics 2008, 70, 486. <https://doi.org/10.1016/j.ejpb.2008.05.022>
• Hoffmann Katrin, Czapp Marion, Löscher Wolfgang: Increase in antiepileptic efficacy during prolonged treatment with valproic acid: Role of inhibition of histone deacetylases?. Epilepsy Research 2008, 81, 107. <https://doi.org/10.1016/j.eplepsyres.2008.04.019>
• Lamarre Mélanie, Desrosiers Richard R.: Up-regulation of protein l-isoaspartyl methyltransferase expression by lithium is mediated by glycogen synthase kinase-3 inactivation and \u03b2-catenin stabilization. Neuropharmacology 2008, 55, 669. <https://doi.org/10.1016/j.neuropharm.2008.05.033>
• Krogenæs A.K., Taubøll E., Stien A., Oskam I.C., Lyche J.L., Dahl E., Thomassen R.F., Sweeney T., Ropstad E.: Valproate affects reproductive endocrine function, testis diameter and some semen variables in non-epileptic adolescent goat bucks. Theriogenology 2008, 70, 15. <https://doi.org/10.1016/j.theriogenology.2008.01.029>
• Ikeda Masaaki: Effects of moodstabilizer on the circadian system: possible implication for abnormalities in mood disorders. Folia Pharmacol. Jpn. 2007, 130, 469. <https://doi.org/10.1254/fpj.130.469>