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Vecchi, Edoardo; Pospisil, Lukas; Albrecht, Steffen et al.

eSPA plus : Scalable Entropy-Optimal Machine Learning Classification for Small Data Problems

NEURAL COMPUTATION. Bd. 34. H. 5. 2022 S. 1220-1255


Globig, Anna-Maria; Strohmeier, Valentina; Surabattula, Rambabu et al.

Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency

JOURNAL OF CLINICAL IMMUNOLOGY. Bd. 42. H. 8. 2022 S. 1626-1637


Seiler, Johannes P-H; Dan, Ohad; Tuscher, Oliver et al.

Experienced entropy drives choice behavior in a boring decision-making task

SCIENTIFIC REPORTS. Bd. 12. H. 1. 2022


Schmitt, Daniel; Bozkurt, Sueleyman; Henning-Domres, Pascale et al.

FACS-mediated isolation of native autophagic vesicles

AUTOPHAGY. 2022


Rajlic, Sanela; Surmann, Luise; Zimmermann, Pia et al.

Fatty Acid Amide Hydrolase Deficiency Is Associated with Deleterious Cardiac Effects after Myocardial Ischemia and Reperfusion in Mice

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. Bd. 23. H. 20. 2022


Rajilic, S; Surmann, L; Zimmermann, P et al.

Fettsäureamid-Hydrolase-Mangel ist assoziiertSchädliche Wirkungen auf das Herz nach Myokardischämie undReperfusion bei Mäu

International Journal of Molecular Sciences. Bd. 23. 2022 S. 1


Lassen, Pierre Bel; Nori, Nicole; Bedossa, Pierre et al.

Fibrogenesis Marker PRO-C3 Is Higher in Advanced Liver Fibrosis and Improves in Patients Undergoing Bariatric Surgery

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. Bd. 107. H. 4. 2022 S. E1356-E1366


Schmitt, Sascha; Huppertsberg, Anne; Klefenz, Adrian et al.

Fluorescence Correlation Spectroscopy Monitors the Fate of Degradable Nanocarriers in the Blood Stream

BIOMACROMOLECULES. Bd. 23. H. 3. 2022 S. 1065-1074


Verleden, Stijn E.; Braubach, Peter; Werlein, Christopher et al.

From Macroscopy to Ultrastructure: An Integrative Approach to Pulmonary Pathology

FRONTIERS IN MEDICINE. Bd. 9. 2022


Treimer, Ernestine; Kalayci, Tugba; Schumann, Sven et al.

Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome

HUMAN MUTATION. Bd. 43. H. 12. 2022 S. 1866-1871