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Bioresearch Open Access|January 1, 2014
HIV-Specific CD8(+) T Lymphocytes in Blood of Long-Term HIV-Infected Hemophilia PatientsVolker Daniel, Sabine Scherer, Mahmoud Sadeghi, et al.
Journal of Comparative Pathology|March 28, 2015
Prototheca zopfii Genotype 2-induced Nasal Dermatitis in a CatN Huth, R F Wenkel, N Roschanski, et al.
Viral Immunology|February 4, 2010
Increased peripheral blood leukocyte subsets with regulatory phenotype in clinically stable long-term HIV-infected hemophilia patients on HAART may be beneficial and contribute to a decrease in autoimmunityVolker Daniel, Cord Naujokat, Mahmoud Sadeghi, et al.
The British Journal of Developmental Psychology|April 1, 2025
Parenting reflectivity and mind-mindedness as unique predictors of children's attachment security and social-emotional developmentJerrica Pitzen, Jamie Lawler, Chong Man Chow, et al.
The Journal of Nervous and Mental Disease|March 28, 2022
Changes in Defense Mechanisms in Mothers From Pregnancy to 2 Years PostpregnancyJohn H Porcerelli, Laura A Richardson, Justin D Smith, et al.
The Journal of Chemical Physics|July 10, 2010
Observation of low heat capacities for vapor-deposited glasses of indomethacin as determined by AC nanocalorimetryKenneth L Kearns, Katherine R Whitaker, M D Ediger, et al.
Nucleic Acids Research|April 2, 1999
Tissue-specific translational regulation of alternative rabbit 15-lipoxygenase mRNAs differing in their 3'-untranslated regionsB J Thiele, M Berger, A Huth, et al.
European Journal of Clinical Pharmacology|August 9, 2019
Siponimod pharmacokinetics, safety, and tolerability in combination with the potent CYP3A4 inhibitor itraconazole in healthy subjects with different CYP2C9 genotypesAnne Gardin, Kasra Shakeri-Nejad, Andrea Feller, et al.
Archives of Orthopaedic and Trauma Surgery|April 21, 2017
Influence of tibial hybrid fixation on graft tension and stability in ACL double-bundle reconstructionB H Drews, A Seitz, J Huth, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 26, 2006
Identification of a novel compound heterozygote SCO2 mutation in cytochrome c oxidase deficient fatal infantile cardioencephalomyopathyM Knuf, J Faber, R G Huth, et al.
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