Publications by authors named "H Gross"

The biosynthesis of cyclic 3',5'-adenosine monophosphate (cAMP) by mammalian membrane-bound adenylyl cyclases (mACs) is predominantly regulated by G-protein-coupled receptors (GPCRs). Up to now the two hexahelical transmembrane domains of mACs were considered to fix the enzyme to membranes. Here, we show that the transmembrane domains serve in addition as signal receptors and transmitters of lipid signals that control Gsα-stimulated mAC activities.

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Article Synopsis
  • A phase 2 clinical trial tested the cyclin-dependent kinase inhibitor SCH 727965 in patients with metastatic melanoma to assess its safety and effectiveness, focusing on overall survival and progression-free survival rates.* -
  • Among 72 enrolled patients, there were no observed responses to the treatment out of 67 evaluable cases, with stable disease in only 21%, median progression-free survival at 1.4 months, and median overall survival at 8.2 months.* -
  • Despite some patients achieving a 1-year overall survival rate of 38%, the study concluded that SCH 727965 showed minimal benefit and significant toxic effects, suggesting it should not be further pursued as a single-agent therapy.*
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In this paper the development of a miniaturized endoscopic objective lens for various biophotonics applications is presented. While limiting the mechanical dimensions to 2.2 mm diameter and 13 mm total length, a numerical aperture of 0.

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Aim: The increased availability of genome sequences has enabled the development of valuable tools for the prediction and identification of bacterial natural products. Burkholderia catarinensis 89T produces siderophores and an unknown potent antifungal metabolite. The aim of this work was to identify and purify natural products of B.

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Fast liquid chromatography (LC) amino acid enantiomer separation of 6-aminoquinolyl--hydroxysuccinimidyl carbamate (AQC) derivatives using a chiral core-shell particle tandem column with weak anion exchange and zwitterionic-type quinine carbamate selectors in less than 3 min was achieved. Enantiomers of all AQC-derivatized proteinogenic amino acids and some isomeric ones (24 in total plus achiral glycine) were baseline separated ( > 1.5 except for glutamic acid with = 1.

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