Results 61 to 70 of about 1,298,581 (123)

Brief von Michael Barth an Kurt Rothschild

BRIEF VON MICHAEL BARTH AN KURT ROTHSCHILD Brief von Michael Barth an Kurt Rothschild ([1]
Barth, Michael
core   +3 more sources

Dynamic simulation of cardiolipin remodeling: greasing the wheels for an interpretative approach to lipidomics[S]

Journal of Lipid Research, 2010
Cardiolipin is a class of mitochondrial specific phospholipid, which is intricately involved in mitochondrial functionality. Differences in cardiolipin species exist in a variety of tissues and diseases.
Michael A. Kiebish, Rob Bell, Kui Yang, Toan Phan, Zhongdan Zhao, William Ames, Thomas N. Seyfried, Richard W. Gross, Jeffrey H. Chuang, Xianlin Han   +9 more
doaj   +1 more source

Guidelines or Other Guidance Documents for Rare Diseases in the Netherlands: When and Where to Invest (Effort, Time and Money)?

Clinical and Public Health Guidelines, Volume 3, Issue 3, July 2026.
ABSTRACT Introduction Developing Clinical Practice Guidelines (CPGs) is resource‐intensive, making it essential to prioritise those CPG projects that are most needed. One of the rules pertains to prevalence, which excludes virtually all guideline development for rare diseases. Still, guidance is needed for their management.
Iméze J. Hieltjes, Charlotte M. W. Gaasterland, Marieke Hermsen, Anne Marie van Wermeskerken, Ilse van Herk, Johanna H. van der Lee   +5 more
wiley   +1 more source

Aberrant TMPRSS6‐Protease Regulation of Disease Mutant HCN4–KCNE1 Channel Complex Depends on the KCNE1‐G38S Polymorphism

Archiv der Pharmazie, Volume 359, Issue 6, June 2026.
TMPRSS6‐mediated cleavage of the HCN4–KCNE1 channel complex may modulate disease phenotype in a KCNE1 genotype‐dependent manner. ABSTRACT The sinoatrial node pacemaker channel HCN4 plays a central role in cardiac automaticity, and disease‐associated variants can predispose to atrial arrhythmias.
David Linhoff, Minay Mertens, Ricarda Zimmermann, Stefan Peischard, Christoph Brenker, Thomas Budde, Sven Meuth, Christos Gatsogiannis, Annika Lüttjohann, Liudmila Sosulina, Jürgen Hescheler, Nathalie Strutz‐Seebohm, Guiscard Seebohm   +12 more
wiley   +1 more source

Johann August Ehrlichs Chirurgische, auf Reisen, vorzüglich in den Hospitälern zu London gemachte Beobachtungen : nebst Angabe verbesserter Operationsarten und Abbildung neuer Instrumente

Vorlageform des Erscheinungsvermerks: Leipzig, bey Johann Ambrosius Barth. 1795.Ill. (Kupferst.
Ehrlich, Johann August
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Précis from Theodor Barth’s doctoral process with Fredrik Barth

, 2021
The flyers feature a data-set processing and modelling its contents in 6 steps: 1) attempt; 2) try again; 3) do something else; 4) return; 5) unlearn; 6) crossover.This flyer series (1 HEX) is a précis from a tutorial process with Prof. Fredrik Barth. It
Barth, Theodor
core  

Evaluating Continuous Glucose Monitoring (CGM) Derived Glucose Variability in Athletes Clinically Diagnosed With Relative Energy Deficiency in Sport (REDs)

European Journal of Sport Science, Volume 26, Issue 6, June 2026.
ABSTRACT Relative Energy Deficiency in Sport (REDs) is a multifactorial condition with significant long‐term health and performance implications. Acute low energy availability (LEA) may suppress glucose levels, particularly nocturnally; however, this has not been investigated in athletes with clinically diagnosed REDs.
Penelope A. Matkin‐Hussey, Dane F. Baker, Gregory R. Cox, Vernon Coffey, Amy‐Lee Bowler, Sarah Beable, Megan Ogilvie, Katherine E. Black   +7 more
wiley   +1 more source

Chirurgische Beobachtungen : nebst hinzugefügter Beschreibung der in England gebräuchlichen Charpiemaschine

Vorlageform des Erscheinungsvermerks: Leipzig, bey Johann Ambrosius Barth. 1815.3 Ill.
Ehrlich, Johann August
core   +1 more source

Johann Christoph Maiers ... Beschreibung von Venedig : Mit Grundrissen und Kupfern

Vorlageform des Erscheinungsvermerks: Leipzig, bei Johann Ambrosius Barth 1795.Titelkupfer, Kt. (Kupferst.
Maier, Johann Christoph
core   +1 more source

AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome

Molecular Therapy: Methods & Clinical Development, 2019
Barth syndrome (BTHS) is a rare mitochondrial disease that causes severe cardiomyopathy and has no disease-modifying therapy. It is caused by recessive mutations in the gene tafazzin (TAZ), which encodes tafazzin—an acyltransferase that remodels the ...
Silveli Suzuki-Hatano, Madhurima Saha, Meghan S. Soustek, Peter B. Kang, Barry J. Byrne, W. Todd Cade, Christina A. Pacak   +6 more
doaj   +1 more source