ThT 101: a primer on the use of thioflavin T to investigate amyloid formation (Englisch)
- Neue Suche nach: Gade Malmos, Kirsten
- Neue Suche nach: Blancas-Mejia, Luis M.
- Neue Suche nach: Weber, Benedikt
- Neue Suche nach: Buchner, Johannes
- Neue Suche nach: Ramirez-Alvarado, Marina
- Neue Suche nach: Naiki, Hironobu
- Neue Suche nach: Otzen, Daniel
- Neue Suche nach: Gade Malmos, Kirsten
- Neue Suche nach: Blancas-Mejia, Luis M.
- Neue Suche nach: Weber, Benedikt
- Neue Suche nach: Buchner, Johannes
- Neue Suche nach: Ramirez-Alvarado, Marina
- Neue Suche nach: Naiki, Hironobu
- Neue Suche nach: Otzen, Daniel
In:
Amyloid
;
24
, 1
;
1-16
;
2017
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:ThT 101: a primer on the use of thioflavin T to investigate amyloid formation
-
Beteiligte:Gade Malmos, Kirsten ( Autor:in ) / Blancas-Mejia, Luis M. ( Autor:in ) / Weber, Benedikt ( Autor:in ) / Buchner, Johannes ( Autor:in ) / Ramirez-Alvarado, Marina ( Autor:in ) / Naiki, Hironobu ( Autor:in ) / Otzen, Daniel ( Autor:in )
-
Erschienen in:Amyloid ; 24, 1 ; 1-16
-
Verlag:
- Neue Suche nach: Taylor & Francis
-
Erscheinungsdatum:02.01.2017
-
Format / Umfang:16 pages
-
ISSN:
-
DOI:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
-
Sprache:Englisch
-
Schlagwörter:
-
Datenquelle:
Inhaltsverzeichnis – Band 24, Ausgabe 1
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 1
-
ThT 101: a primer on the use of thioflavin T to investigate amyloid formationGade Malmos, Kirsten / Blancas-Mejia, Luis M. / Weber, Benedikt / Buchner, Johannes / Ramirez-Alvarado, Marina / Naiki, Hironobu / Otzen, Daniel et al. | 2017
- 17
-
Marked biochemical difference in amyloid proportion between intra- and extraocular tissues in a liver-transplanted patient with hereditary ATTR amyloidosisYoshinaga, Tsuneaki / Yazaki, Masahide / Kametani, Fuyuki / Sekijima, Yoshiki / Iesato, Yasuhiro / Miyahara, Teruyoshi / Tsuchiya-Suzuki, Ayako / Sano, Kenji / Higuchi, Keiichi / Ikeda, Shu-ichi et al. | 2017
- 24
-
Clinicopathological and biochemical findings of thyroid amyloid in hereditary transthyretin amyloidosis with and without liver transplantationHuang, Guannan / Ueda, Mitsuharu / Tasaki, Masayoshi / Yamashita, Taro / Misumi, Yohei / Masuda, Teruaki / Suenaga, Genki / Inoue, Yasuteru / Kinoshita, Yumiko / Matsumoto, Sayaka et al. | 2017
- 30
-
Tafamidis delays disease progression in patients with early stage transthyretin familial amyloid polyneuropathy: additional supportive analyses from the pivotal trialKeohane, Denis / Schwartz, Jeffrey / Gundapaneni, Balarama / Stewart, Michelle / Amass, Leslie et al. | 2017
- 37
-
Transbronchial biopsies safely diagnose amyloid lung diseaseGovender, Praveen / Keyes, Colleen M. / Hankinson, Elizabeth A. / O’Hara, Carl J. / Sanchorawala, Vaishali / Berk, John L. et al. | 2017
- 42
-
CSP-1103 (CHF5074) stabilizes human transthyretin in healthy human subjectsQiang, Lixia / Guan, Yanxia / Li, Xiangshun / Liu, Li / Mu, Yanshuang / Sugano, Aki / Takaoka, Yutaka / Sakaeda, Toshiyuki / Imbimbo, Bruno P. / Yamamura, Ken-Ichi et al. | 2017
- 52
-
Amyloid in bone marrow smears in systemic light-chain amyloidosisKimmich, Christoph / Schönland, Stefan / Kräker, Sandra / Andrulis, Mindaugas / Ho, Anthony D. / Mayer, Gudrun / Dittrich, Tobias / Hundemer, Michael / Hegenbart, Ute et al. | 2017
- 60
-
Complex p.T88N/W130R mutation in the lysozyme gene leading to hereditary lysozyme amyloidosis with biopsy-proven cardiac involvementSperry, Brett W. / Dispenzieri, Angela / Ikram, Asad / Grogan, Martha / Theis, Jason D. / Leung, Nelson / Highsmith, W. Edward / Maleszewski, Joseph J. / Hanna, Mazen et al. | 2017
- 62
-
Tocilizumab postpones the start of hemodialysis compared to conventional oral treatment in amyloid A amyloidosis patients with advanced renal insufficiency by suppressing serum SAA levelsUda, Hiroshi / Saiki, Osamu et al. | 2017
- 64
-
Hereditary amyloid polyneuropathy-related destructive arthropathy in a hip jointSato, Shunichi / Seki, Hifumi / Ikeda, Shu-ichi et al. | 2017
- 66
-
Pseudo-homozygous mutation due to a primer site polymorphism in hereditary ATTR amyloidosis: a pitfall of PCR-based genetic testingShibata, Yuka / Matsushima, Masaaki / Yabe, Ichiro / Matsuda, Koichiro / Nagai, Azusa / Kano, Takahiro / Yamada, Takahiro / Sekijima, Yoshiki / Sasaki, Hidenao et al. | 2017
- 68
-
Cathepsin K as a novel amyloid fibril protein in humansLinke, Reinhold P. / Serpell, Louise C. / Lottspeich, Friedrich / Toyoda, Mitsuyasu et al. | 2017
- 70
-
Phenotypic characterization of late onset cardiac amyloidosis caused by the transthyretin mutation TTRA45S, p.(Ala65Ser)Müllertz, Katrine M. / Baerentzen, Steen / Jensen, Henrik K. / Mølgaard, Henning et al. | 2017