- Comparison of antiaggregatory effects of PGI2, PGI3 and iloprost on human and rabbit plateletsKobzar, Gennadi; Mardla, Vilja; Järving, Ivar; Samel, NigulasCellular physiology and biochemistry2001 / 5, p. 279-284 https://pubmed.ncbi.nlm.nih.gov/11684817/
- (Eco)toxicological information on REACH-relevant chemicals : contribution of alternative methods to in vivo approachesSihtmäe, Mariliis2011 http://www.ester.ee/record=b2733161*est
- Efedrooni (metkatinoon) ja mangaani toime hiirtel kroonilises katses : [TÜ arstiteaduskonna päeva 2009 stendiettekande teesid]Asser, Andres; Kõks, Sulev; Nairismägi, JaakEesti Arst2009 / 9, lk. 612-613 https://artiklid.elnet.ee/record=b1496051*est
- Expression analysis of the CLCA gene family in mouse and human with emphasis on the nervous systemPiirsoo, Marko; Meijer, Dies; Timmusk, TõnisBMC developmental biology2009 / p. 10 : ill https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2653474/
- Expression of neurotrophin receptors in rat testis. Upregulation of TrkA mRNA with hCG treatmentSchultz, R.; Metsis, Madis; Hokfelt, T.; Parvinen, M.; Pelto-Huikko, M.Molecular and cellular endocrinology2001 / p. 121-127 https://pubmed.ncbi.nlm.nih.gov/11500245/
- Functional characterization of two splice variants of rat Bad and their interaction with Bcl-w in sympathetic neuronsHamner, S.; Arumäe, Urmas; Li-Ying, Y.; Sun, Yun-Fu; Saarma, Mart; Lindholm, DanMolecular and cellular neurosciences2001 / p. 97-106 https://pubmed.ncbi.nlm.nih.gov/11161472/
- GDNF family ligands and receptors are differentially regulated after brain insults in the ratKokaia, Zaal; Airaksinen, Matti S.; Nanobashvili, A.; Larsson, E.; Kujamäki, E.; Lindvall, O.; Saarma, MartEuropean journal of neuroscience1999 / p. 1202-1216
- GDNF family receptors in the embryonic and postnatal rat heart and reduced cholinergic innervation in mice hearts lacking Ret or GFRa2Hiltunen, J.O.; Laurikainen, A.; Airaksinen, Matti S.; Saarma, MartDevelopmental dynamics2000 / p. 28-39 https://pubmed.ncbi.nlm.nih.gov/10974669/
- Glial cell line-derived neurotrophic factor is expressed in penis of adult rat and retrogradely transported in penile parasympathetic and sensory nervesLaurikainen, A.; Hiltunen, J.O.; Vanhatalo, S.; Klinge, E.; Saarma, MartCell and tissue research2000 / p. 321-329 https://pubmed.ncbi.nlm.nih.gov/11151444/
- Increased extracellular dopamine concentrations and FosB/DeltaFosB expression in striatal brain areas of heterozygous GDNF knockout miceAiravaara, Mikko; Planken, Anu; Gäddnäs, Helena; Piepponen, Timo Petteri; Saarma, Mart; Ahtee, LiisaEuropean journal of neuroscience2004 / 9, p. 2336-2344 : ill https://pubmed.ncbi.nlm.nih.gov/15525275/
- Long-lasting behavioural and molecular alterations induced by early postnatal fluxetine exposure are restored by chronic fluxetine treatment in adult miceKarpova, Nina N.; Lindholm, Jesse; Pruunsild, Priit; Timmusk, Tõnis; Castren, EeroEuropean neuropsychopharmacology2009 / p. 97-108 : ill https://pubmed.ncbi.nlm.nih.gov/18973993/
- Magnetic resonance imaging study of induced epileptogenesis in animal models of epilepsyNairismägi, Jaak2006 https://www.ester.ee/record=b4369104*est
- Missense mutations in the extracellular domain of the human neural cell adhesion molecule L1 reduce neurite outgrowth of murine cerebellar neuronsMichelson, P.; Veske, AndresHuman mutations2002 / 6, p. 481-482 https://pubmed.ncbi.nlm.nih.gov/12442287/
- Nerve growth factor and brain-derived neurotrophic factor mRNAs are regulated in distinct cell populations of rat heart after ischaemia and reperfusionHiltunen, J.O.; Laurikainen, A.; Väkeva, A.; Meri, S.; Saarma, MartJournal of pathology2001 / p. 247-253 https://pubmed.ncbi.nlm.nih.gov/11400155/
- Neurturin is a neurotrophic factor for penile parasympathetic neurons in adult ratLaurikainen, A.; Hiltunen, J.O.; Thomas-Crusells, J.; Vanhatalo, S.; Arumäe, Urmas; Airaksinen, Matti S.; Klinge, E.; Saarma, MartJournal of neurobiology2000 / p. 198-205 https://pubmed.ncbi.nlm.nih.gov/10770848/
- Nuclear factor of activated T-cells isoform c4 (NFATc4/NFAT3) as a mediator of anti-apoptotic transcription in NMDA receptor-stimulated cortical neuronsVashishta, Aruna; Habas, Agata; Pruunsild, Priit; Zheng, Jing-Juan; Timmusk, Tõnis; Hetman, MichalJournal of neuroscience2009 / 48, p. 15331-15340 https://pubmed.ncbi.nlm.nih.gov/19955386/
- Overcoming donor variability and risks associated with fecal microbiota transplants through bacteriophage-mediated treatmentsRasmussen, Torben Sølbeck; Mao, Xiaotian; Forster, Sarah; Larsen, Sabina Birgitte; Von Münchow, Alexandra; Tranæs, Kaare Dyekær; Brunse, Anders; Larsen, Frej; Mejia, Josue Leonardo Castro; Adamberg, Signe; Hansen, Axel Kornerup; Adamberg, Kaarel; Hansen, Camilla Hartmann Friis; Nielsen, Dennis SandrisMicrobiome2024 / art. 119 https://doi.org/10.1186/s40168-024-01820-1
- P2X4 and P2X7 receptors in evolution, physiology, inflammation, and autoimmunity = P2X4 ja P2X7 retseptorid evolutsiooni, füsioloogia, põletiku ja autoimmuunsuse kontekstisRump, Airi2023 https://doi.org/10.23658/taltech.53/2023 https://digikogu.taltech.ee/et/Item/d5c7f19b-53ae-4010-9249-2aa0b04b898e https://www.ester.ee/record=b5645330*est
- P75 neurotrophin receptor signaling activates sterol regulatory element-binding protein-2 in hepatocyte cells via p38 mitogen-activated protein kinase and caspase-3Pham, Dan Duc; Do, Hai Thi; Bruelle, Céline; Kukkonen, Jyrki P.; Eriksson, Ove; Mogollón, Isabel; Korhonen, Laura T.; Arumäe, Urmas; Lindholm, DanJournal of Biological Chemistry2016 / p. 10747 - 10758 https://doi.org/10.1074/jbc.M116.722272 https://www.scopus.com/sourceid/17592 https://www.scopus.com/record/display.uri?eid=2-s2.0-84969242869&origin=resultslist&sort=plf-f&src=s&sid=f0c1c3413f201be0255f920efdc168f9&sot=b&sdt=b&s=DOI%2810.1074%2Fjbc.M116.722272%29&sl=30&sessionSearchId=f0c1c3413f201be0255f920efdc168f9&relpos=0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20BIOL%20CHEM&year=2016 https://www.webofscience.com/wos/woscc/full-record/WOS:000377042600026
- PSPN/GFR[alpha]4 has a significantly weaker capacity than GDNF/GFR[alpha]1 to recruit RET to rafts, but promotes neuronal survival and neurite outgrowthYang, Jianmin; Lindahl, Maria; Lindholm, Päivi; Virtanen, Heidi; Coffey, Eleanor; Runeberg-Roos, Pia; Saarma, MartFEBS letters2004 / 1/3, p. 267-271 : ill https://pubmed.ncbi.nlm.nih.gov/15225646/
- Seizures induce widespread upregulation of cystatin B, the gene mutated in progressive myoclonus epilepsy, in rat forebrain neuronsD'Amato, E.; Kokaia, Zaal; Nanobashvili, A.; Reeben, M.; Lehesjoki, A.-E.; Saarma, Mart; Lindvall, O.European journal of neuroscience2000 / p. 1687-1695 https://pubmed.ncbi.nlm.nih.gov/10792446/
- Structure, alternative splicing, and expression of the human and mouse KCNIP gene familyPruunsild, Priit; Timmusk, TõnisGenomics2005 / 5, p. 581-593 https://pubmed.ncbi.nlm.nih.gov/16112838/
- The messenger RNAs for both glial cell line-derived neurotrophic factor receptors, C-ret and GDNFR, are induced in the rat brain in response to Kainate-induced excitationReeben, M.; Laurikainen, A.; Hiltunen, J.O.; Castren, Eero; Saarma, MartNeuroscience1998 / p. 151-159
- The native copper- and zinc- binding protein metallothionein blocks copper-mediated A[beeta] aggregation and toxicity in rat cortical neuronsChung, Roger S.; Howells, Claire; Zovo, Kairit; Palumaa, Peep; Sillard, RannarPLoS ONE2010 / 8, p. e12030 [11 p.] https://pmc.ncbi.nlm.nih.gov/articles/PMC2920313/
- Transcriptional repression of neurotrophin receptor trkB by thyroid hormone in the developing rat brainPombo, P.M.; Barettino, D.; Espliguero, G.; Metsis, Madis; Iglesias, T.; Rodriguez-Pena, A.Journal of biological chemistry2000 / p. 37510-37517 https://pubmed.ncbi.nlm.nih.gov/10978336/
- Transfer of modified gut viromes improves symptoms associated with metabolic syndrome in obese male miceMao, Xiaotian; Larsen, Sabina Birgitte; Zachariassen, Line Sidsel Fisker; Brunse, Anders; Adamberg, Signe; Mejia, Josue Leonardo Castro; Larsen, Frej; Adamberg, Kaarel; Nielsen, Dennis Sandris; Hansen, Axel Kornerup; Hansen, Camilla Hartmann Friis; Rasmussen, Torben SølbeckNature communications2024 / art. 4704 https://doi.org/10.1038/s41467-024-49152-w https://www.scopus.com/sourceid/19700182758 https://www.scopus.com/pages/publications/85195006914?inward https://jcr.clarivate.com/jcr-jp/journal-profile?journal=NAT%20COMMUN&year=2024 https://www.webofscience.com/wos/woscc/full-record/WOS:001238270100005