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Author/Creator Goswami, Anand

1. Accumulation of STIM1 is associated with the degenerative muscle fibre phenotype in ALS and other neurogenic atrophies. (April 2015)

Authors:
Goswami, Anand; Jesse, Christofer Marvin; Chandrasekar, Akila; Bushuven, Eva; Vollrath, Jan Tilmann; Dreser, Alice; Katona, Istvan; Beyer, Cordian; Johann, Sonja; Feller, A. C.; Grond, M.; Wagner, S.; Nikolin, Stefan; Troost, Dirk; Weis, Joachim
Journal:
Neuropathology & applied neurobiology
Issue:
Volume 41:Number 3(2015)
Page Start:
304
Record Type:
Journal Article
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2. Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations. Issue 3 (9th July 2016)

Authors:
Rudnik‐Schöneborn, Sabine; Deden, Florian; Eggermann, Katja; Eggermann, Thomas; Wieczorek, Dagmar; Sellhaus, Bernd; Yamoah, Alfred; Goswami, Anand; Claeys, Kristl G.; Weis, Joachim; Zerres, Klaus
Journal:
Muscle & nerve
Issue:
Volume 54:Issue 3(2016)
Page Start:
496
Record Type:
Journal Article
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3. Cuprizone‐induced graded oligodendrocyte vulnerability is regulated by the transcription factor DNA damage‐inducible transcript 3. Issue 2 (3rd December 2018)

Authors:
Fischbach, Felix; Nedelcu, Julia; Leopold, Patrizia; Zhan, Jiangshan; Clarner, Tim; Nellessen, Lara; Beißel, Christian; van Heuvel, Yasemin; Goswami, Anand; Weis, Joachim; Denecke, Bernd; Schmitz, Christoph; Hochstrasser, Tanja; Nyamoya, Stella; Victor, Marion; Beyer, Cordian; Kipp, Markus
Journal:
Glia
Issue:
Volume 67:Issue 2(2019)
Page Start:
263
Record Type:
Journal Article
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4. Hsp90‐mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling. (19th March 2021)

Authors:
Mediani, Laura; Antoniani, Francesco; Galli, Veronica; Vinet, Jonathan; Carrà, Arianna Dorotea; Bigi, Ilaria; Tripathy, Vadreenath; Tiago, Tatiana; Cimino, Marco; Leo, Giuseppina; Amen, Triana; Kaganovich, Daniel; Cereda, Cristina; Pansarasa, Orietta; Mandrioli, Jessica; Tripathi, Priyanka; Troos...
Journal:
EMBO reports
Issue:
Volume 22:Number 5(2021)
Page Start:
n/a
Record Type:
Journal Article
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7. Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis. Issue 12 (4th November 2019)

Authors:
Naumann, Marcel; Peikert, Kevin; Günther, Rene; van der Kooi, Anneke J.; Aronica, Eleonora; Hübers, Annemarie; Danel, Veronique; Corcia, Philippe; Pan‐Montojo, Francisco; Cirak, Sebahattin; Haliloglu, Göknur; Ludolph, Albert C.; Goswami, Anand; Andersen, Peter M.; Prudlo, Johannes; Wegner, Floria...
Journal:
Annals of clinical and translational neurology
Issue:
Volume 6:Issue 12(2019)
Page Start:
2384
Record Type:
Journal Article
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