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- Kluytmans, J, et al.
(författare)
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Obituary: Johan Willem Mouton
- 2020
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Ingår i: CLINICAL MICROBIOLOGY AND INFECTION. - : Elsevier BV. - 1198-743X. ; 26:1, s. 125-126
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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- Gregersen, S., et al.
(författare)
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Physical differences in the deep lithosphere of Northern and Central Europe
- 2006. - 32
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Ingår i: European Lithosphere Dynamics. - : Geological Society of London. - 9781862392120 - 1862392129 ; 32, s. 313-322
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- A number of large-scale integrated studies, including the TOR and POLONAISE’97 projects, with an emphasis on seismicmethods, have been used to elucidate the southwestern boundary (suture zone) between the East European Craton and the Phanerozoicterranes of Western Europe. Results indicate that a thick slab of mantle lithosphere below the craton thins southwestwards beneath theTrans-European Suture Zone and is not seen south of the Variscan front. The thinning is not gradual, but is interrupted by at least twoabrupt deep boundaries, the most significant of which corresponds to the surface position of the Tornquist Zone, a major fault. Thepresent geometry of the lithosphere is the result of modification of the margin of the Neoproterozoic continent Baltica by Phanerozoicprocesses, including the development of the Tornquist Zone and the stretching of the lithosphere in a broad central block SW of thiszone. Seismic results and their interpretations from the TOR tomographic project are presented and compared with results from thePOLONAISE’97 controlled source project to the SE. Both investigations have shown high-angle, non-symmetrical features extendingdeep into the mantle.
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- Lindelof, H, et al.
(författare)
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Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up
- 2022
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Ingår i: Frontiers in endocrinology. - : Frontiers Media SA. - 1664-2392. ; 13, s. 862908-
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Nail-patella syndrome (NPS, OMIM #161200) is a rare autosomal dominant disorder with symptoms from many different parts of the body, including nails, knees, elbows, pelvis, kidneys and eyes. It is caused by truncating variants in the LMX1B gene, which encodes a transcription factor with important roles during embryonic development, including dorsoventral patterning of the limbs. To our knowledge, inversions disrupting the LMX1B gene have not been reported. Here, we report a family with an inversion disrupting the LMX1B gene in five affected family members with mild but variable clinical features of NPS. Our finding demonstrates that genomic rearrangements must be considered a possible cause of NPS.
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- Voss, Ulrikke, et al.
(författare)
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Effects of dietary fibers on the tuft cell population in the mouse colon post radiation
- 2019
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Ingår i: Neurogastroenterology and Motility. - : Wiley. - 1365-2982 .- 1350-1925. ; 31:S4, s. 150-150
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Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
- Pelvic radiation therapy is often associated with gastrointestinal dysfunction. Intestinal tuft cell located within the mucosal epithelium have in the small intestine following full body radiation in mice been shown to be essential for epithelial regeneration. Dietary approaches during and after radiation therapy have also been suggested to aid epithelial health and function. Tuft cells are suggested to be important for translation of chemosensory signals in the lumen. This study investigated the effects of dietary fiber composition on tuft cell numbers in the colon at 1, 6 and 18 weeks post radiation.
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