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The Journal of Biological Chemistry|July 29, 2011
Cellular content of UDP-N-acetylhexosamines controls hyaluronan synthase 2 expression and correlates with O-linked N-acetylglucosamine modification of transcription factors YY1 and SP1Tiina A Jokela, Katri M Makkonen, Sanna Oikari, et al.
Plos Genetics|June 27, 2015
Abnormal Activation of BMP Signaling Causes Myopathy in Fbn2 Null MiceGerhard Sengle, Valerie Carlberg, Sara F Tufa, et al.
The Journal of Nutritional Biochemistry|May 24, 2014
Primary vitamin D receptor target genes as biomarkers for the vitamin D3 status in the hematopoietic systemJulia Wilfinger, Sabine Seuter, Tomi-Pekka Tuomainen, et al.
Molecular Nutrition & Food Research|July 1, 2014
Changes in vitamin D target gene expression in adipose tissue monitor the vitamin D response of human individualsJussi Ryynänen, Antonio Neme, Tomi-Pekka Tuomainen, et al.
Pediatric Dermatology|December 30, 2020
Cutaneous reactions to pediatric cancer treatment part II: Targeted therapyValerie M Carlberg, Olivia M T Davies, Heather A Brandling-Bennett, et al.
Molecular Biology of the Cell|November 10, 2000
Colony-stimulating factor-1 receptor utilizes multiple signaling pathways to induce cyclin D2 expressionA Dey, H She, L Kim, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 17, 2012
Inhibition of cytokine secretion from adipocytes by 1,25-dihydroxyvitamin D₃ via the NF-κB pathwayShivaprakash J Mutt, Toni Karhu, Siri Lehtonen, et al.
Scientific Reports|December 4, 2020
Common and personal target genes of the micronutrient vitamin D in primary immune cells from human peripheral bloodAndrea Hanel, Antonio Neme, Marjo Malinen, et al.
AIDS Education and Prevention : Official Publication of the International Society for AIDS Education|June 25, 2024
Long-Term Impacts on Clinical Practice Along the HIV Care Continuum: Addressing Workforce Gaps Through a Clinician Scholars ProgramSuzanne Carlberg-Racich, Ricardo Rivero, Cornelia M J Wagner, et al.
Genomics|July 15, 1997
Two distinct deletions in the IDS gene and the gene W: a novel type of mutation associated with the Hunter syndromeS L Karsten, K Lagerstedt, B M Carlberg, et al.
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