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Document Title Author Full Name Author Short Name Index Corresponding Address ResearcherID ResearcherID Author Name ORCID ORCID Author Name Related Email
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Uebe, Steffen Uebe, S 10 Friedrich Alexander Univ Erlangen Nuremberg, Inst Human Genet, Erlangen, Germany JXX-3960-2024 Uebe, Steffen Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Ekici, Arif B. Ekici, AB 11 Friedrich Alexander Univ Erlangen Nuremberg, Inst Human Genet, Erlangen, Germany C-3971-2013 Ekici, Arif Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Gulbins, Erich Gulbins, E 12 Univ Duisburg Essen, Dept Mol Biol, D-45147 Essen, Germany Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Gulbins, Erich Gulbins, E 12 Univ Cincinnati, Coll Med, Dept Surg, 231 Albert Sabin Way, Cincinnati, OH 45267, USA Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Kornhuber, Johannes Kornhuber, J 13 Friedrich Alexander Univ Erlangen Nuremberg, Univ Clin, Dept Psychiat & Psychotherapy, Erlangen, Germany Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Jin, Hee Kyung Jin, HK 14 Kyungpook Natl Univ, KNU Alzheimers Dis Res Inst, Daegu 41566, South Korea Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Jin, Hee Kyung Jin, HK 14 Kyungpook Natl Univ, Coll Vet Med, Dept Lab Anim Med, Daegu 41566, South Korea Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Bae, Jae-sung Bae, JS 15 Kyungpook Natl Univ, KNU Alzheimers Dis Res Inst, Daegu 41566, South Korea AAM-8663-2021 Bae, Jae-sung Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Bae, Jae-sung Bae, JS 15 Kyungpook Natl Univ, Sch Med, Dept Physiol, Daegu 41944, South Korea AAM-8663-2021 Bae, Jae-sung Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Lourdusamy, Anbarasu Lourdusamy, A 16 Univ Nottingham, Sch Med, Acad Unit Translat Med Sci, Nottingham NG7 2UH, England G-3387-2011 Lourdusamy, Anbarasu Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Mueller, Christian P. Müller, CP 17 교신저자 Friedrich Alexander Univ Erlangen Nuremberg, Univ Clin, Dept Psychiat & Psychotherapy, Erlangen, Germany Christian.Mueller@uk-erlangen.de;
Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia Mueller, Christian P. Müller, CP 17 교신저자 Heidelberg Univ, Cent Inst Mental Hlth, Med Fac Mannheim, Dept Addict Behav & Addict Med, Mannheim, Germany Christian.Mueller@uk-erlangen.de;
ACID SPHINGOMYELINASE FUNCTIONS AS A NOVEL CATABOLIC REGULATOR TO MEDIATE ARTICULAR CHONDROCYTE DEGENERATION VIA DYSREGULATED CHOLESTEROL UPTAKE Che, Xiangguo Che, XG 1 Kyungpook Natl Univ, Cell & Matrix Res Inst, Sch Med, Dept Biochem & Cell Biol, Daegu, South Korea
ACID SPHINGOMYELINASE FUNCTIONS AS A NOVEL CATABOLIC REGULATOR TO MEDIATE ARTICULAR CHONDROCYTE DEGENERATION VIA DYSREGULATED CHOLESTEROL UPTAKE Jin, Xian Jin, X 2 Kyungpook Natl Univ, Cell & Matrix Res Inst, Sch Med, Dept Biochem & Cell Biol, Daegu, South Korea
ACID SPHINGOMYELINASE FUNCTIONS AS A NOVEL CATABOLIC REGULATOR TO MEDIATE ARTICULAR CHONDROCYTE DEGENERATION VIA DYSREGULATED CHOLESTEROL UPTAKE Lee, Dong-Kyo Lee, DK 3 Kyungpook Natl Univ, Cell & Matrix Res Inst, Sch Med, Dept Biochem & Cell Biol, Daegu, South Korea
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