LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 28

Search options

  1. Article ; Online: Correction: Billeaud et al. "Effects on Fatty Acid Metabolism of a New Powdered Human Milk Fortifier Containing Medium-Chain Triacylglycerols and Docosahexaenoic Acid in Preterm Infants"

    Billeaud, Claude / Boué-Vaysse, Carole / Couëdelo, Leslie / Steenhout, Philippe / Jaeger, Jonathan / Cruz-Hernandez, Cristina / Ameye, Laurent / Rigo, Jacques / Picaud, Jean-Charles / Saliba, Elie / Hays, Nicholas P / Destaillats, Frédéric

    Nutrients

    2019  Volume 11, Issue 3

    Abstract: The authors wish to make a correction to the published version of their paper [ ... ]. ...

    Abstract The authors wish to make a correction to the published version of their paper [...].
    Language English
    Publishing date 2019-03-22
    Publishing country Switzerland
    Document type Published Erratum
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu11030680
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Recurrence and Outcome of Anti-Glomerular Basement Membrane Glomerulonephritis After Kidney Transplantation.

    Coche, Sophie / Sprangers, Ben / Van Laecke, Steven / Weekers, Laurent / De Meyer, Vicky / Hellemans, Rachel / Castanares, Diego / Ameye, Heleen / Goffin, Eric / Demoulin, Nathalie / Gillion, Valentine / Mourad, Michel / Darius, Tom / Buemi, Antoine / Devresse, Arnaud / Kanaan, Nada

    Kidney international reports

    2021  Volume 6, Issue 7, Page(s) 1888–1894

    Abstract: Introduction: Recurrence of anti-glomerular basement membrane (anti-GBM) glomerulonephritis in the kidney graft is a rare event, described in limited reports. The aim of this study was to evaluate, in a large cohort of patients with long follow-up, the ... ...

    Abstract Introduction: Recurrence of anti-glomerular basement membrane (anti-GBM) glomerulonephritis in the kidney graft is a rare event, described in limited reports. The aim of this study was to evaluate, in a large cohort of patients with long follow-up, the risk of recurrence of anti-GBM disease, the risk factors associated with clinical recurrence, and the long-term patient and graft survival.
    Methods: This was a multicenter retrospective study. Inclusion criteria were patients with anti-GBM glomerulonephritis who underwent transplantation of a kidney between 1977 and 2015. Exclusion criteria were systemic vasculitis, lupus erythematosus, and cryoglobulinemia. Recurrence was defined as reappearance of clinical signs of glomerulonephritis along with histological signs of proliferative glomerulonephritis and linear IgG staining on kidney biopsy, with or without anti-GBM antibodies.
    Results: A total of 53 patients were included. Recurrence of anti-GBM glomerulonephritis in a first kidney transplant occurred in only 1 patient 5 years after transplantation (a prevalence rate of 1.9%) in the context of cessation of immunosuppressive drugs, and resulted in graft loss due to recurrence. Linear IgG staining on kidney biopsy in the absence of histological signs of proliferative glomerulonephritis was observed in 4 patients, in the context of cellular rejection. Patient survival was 100%, 94%, and 89% at 5, 10, and 15 years, respectively. Death-censored first-graft survival rates were 88%, 83%, and 79% at 5, 10, and 15 years, respectively.
    Conclusion: The recurrence rate of anti-GBM glomerulonephritis after transplantation is very low but is associated with graft loss. The long-term patient and graft survival rates are excellent.
    Language English
    Publishing date 2021-04-28
    Publishing country United States
    Document type Journal Article
    ISSN 2468-0249
    ISSN (online) 2468-0249
    DOI 10.1016/j.ekir.2021.04.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Reply: "Letter to the Editor Re: Billeaud et al.

    Billeaud, Claude / Boué-Vaysse, Carole / Couëdelo, Leslie / Steenhout, Philippe / Jaeger, Jonathan / Cruz-Hernandez, Cristina / Ameye, Laurent / Rigo, Jacques / Picaud, Jean-Charles / Saliba, Elie / Hays, Nicholas P / Destaillats, Frédéric

    Nutrients

    2019  Volume 11, Issue 2

    Abstract: We thank Bernard and colleagues for their careful reading and interest in our ... ...

    Abstract We thank Bernard and colleagues for their careful reading and interest in our article
    MeSH term(s) Arachidonic Acid ; Docosahexaenoic Acids ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Milk, Human ; Nutrients
    Chemical Substances Nutrients ; Docosahexaenoic Acids (25167-62-8) ; Arachidonic Acid (27YG812J1I)
    Language English
    Publishing date 2019-02-15
    Publishing country Switzerland
    Document type Letter
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu11020406
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Fortnightly or fractionated weekly docetaxel-cisplatin-5-FU as first-line treatment in advanced gastric and gastroesophageal junction adenocarcinoma: The randomized phase II DoGE study.

    Deleporte, Amélie / Van den Eynde, Marc / Forget, Frédéric / Holbrechts, Stéphane / Delaunoit, Thierry / Houbiers, Ghislain / Kalantari, Hassan R / Laurent, Stéphanie / Vanderstraeten, Erik / De Man, Marc / Vergauwe, Philippe / Clausse, Marylene / Van Der Auwera, Jacques / D'Hondt, Lionel / Pierre, Pascal / Ghillemijn, Bjorn / Covas, Angelique / Paesmans, Marianne / Ameye, Lieveke /
    Awada, Ahmad / Sclafani, Francesco / Hendlisz, Alain

    Cancer medicine

    2021  Volume 10, Issue 13, Page(s) 4366–4374

    Abstract: Background: While docetaxel/cisplatin/5-fluorouracil (DCF) outperforms CF in first-line gastric adenocarcinoma, toxicity remains an issue.: Methods: This multicenter phase II trial randomized chemonaïve metastatic gastric adenocarcinoma patients to ... ...

    Abstract Background: While docetaxel/cisplatin/5-fluorouracil (DCF) outperforms CF in first-line gastric adenocarcinoma, toxicity remains an issue.
    Methods: This multicenter phase II trial randomized chemonaïve metastatic gastric adenocarcinoma patients to fractionated weekly DCF (D 40 mg/m
    Results: A total of 106 eligible patients were recruited. The early and overall FN rates were 9.5% and 17% in arm 1, respectively, and 5.9% and 8% in arm 2, respectively. Grade ≥3 toxicities occurred in 81% of patients in arm 1 and 90% of patients in arm 2, the most common being neutropenia (33% vs. 61%), fatigue (27% vs. 25%), vomiting (21% vs. 12%), anorexia (19% vs. 18%), and diarrhea (17% vs. 10%). Median progression-free survival and overall survival were 5.1 (95% CI, 3.2-6.5) and 8.2 months (95% CI, 6.0-14.5), respectively, in arm 1 and 5.2 (95% CI, 3.0-6.9) and 11.9 months (95% CI, 7.4-15.9), respectively, in arm 2.
    Conclusions: Fractionated weekly and fortnightly DCF regimens are associated with a low risk of early FN, and a better hematological toxicity profile as compared to historical DCF without compromising efficacy. Both regimens offer greater convenience removing the need for systematic use of prophylactic G-CSF.
    MeSH term(s) Adenocarcinoma/drug therapy ; Adenocarcinoma/mortality ; Adenocarcinoma/pathology ; Adult ; Aged ; Aged, 80 and over ; Anorexia/chemically induced ; Anorexia/epidemiology ; Antineoplastic Combined Chemotherapy Protocols/administration & dosage ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Cisplatin/administration & dosage ; Cisplatin/adverse effects ; Diarrhea/chemically induced ; Diarrhea/epidemiology ; Docetaxel/administration & dosage ; Docetaxel/adverse effects ; Drug Administration Schedule ; Esophagogastric Junction ; Fatigue/chemically induced ; Fatigue/epidemiology ; Febrile Neutropenia/epidemiology ; Female ; Fluorouracil/administration & dosage ; Fluorouracil/adverse effects ; Granulocyte Colony-Stimulating Factor ; Humans ; Male ; Middle Aged ; Neutropenia/chemically induced ; Neutropenia/epidemiology ; Progression-Free Survival ; Stomach Neoplasms/drug therapy ; Stomach Neoplasms/mortality ; Stomach Neoplasms/pathology ; Vomiting/chemically induced ; Vomiting/epidemiology
    Chemical Substances Granulocyte Colony-Stimulating Factor (143011-72-7) ; Docetaxel (15H5577CQD) ; Cisplatin (Q20Q21Q62J) ; Fluorouracil (U3P01618RT)
    Language English
    Publishing date 2021-05-31
    Publishing country United States
    Document type Clinical Trial, Phase II ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2659751-2
    ISSN 2045-7634 ; 2045-7634
    ISSN (online) 2045-7634
    ISSN 2045-7634
    DOI 10.1002/cam4.3976
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Carnosol Inhibits Pro-Inflammatory and Catabolic Mediators of Cartilage Breakdown in Human Osteoarthritic Chondrocytes and Mediates Cross-Talk between Subchondral Bone Osteoblasts and Chondrocytes.

    Sanchez, Christelle / Horcajada, Marie-Noëlle / Membrez Scalfo, Fanny / Ameye, Laurent / Offord, Elizabeth / Henrotin, Yves

    PloS one

    2015  Volume 10, Issue 8, Page(s) e0136118

    Abstract: Aim: The aim of this work was to evaluate the effects of carnosol, a rosemary polyphenol, on pro-inflammatory and catabolic mediators of cartilage breakdown in chondrocytes and via bone-cartilage crosstalk.: Materials and methods: Osteoarthritic (OA) ...

    Abstract Aim: The aim of this work was to evaluate the effects of carnosol, a rosemary polyphenol, on pro-inflammatory and catabolic mediators of cartilage breakdown in chondrocytes and via bone-cartilage crosstalk.
    Materials and methods: Osteoarthritic (OA) human chondrocytes were cultured in alginate beads for 4 days in presence or absence of carnosol (6 nM to 9 μM). The production of aggrecan, matrix metalloproteinase (MMP)-3, tissue inhibitor of metalloproteinase (TIMP)-1, interleukin (IL)-6 and nitric oxide (NO) and the expression of type II collagen and ADAMTS-4 and -5 were analyzed. Human osteoblasts from sclerotic (SC) or non-sclerotic (NSC) subchondral bone were cultured for 3 days in presence or absence of carnosol before co-culture with chondrocytes. Chondrocyte gene expression was analyzed after 4 days of co-culture.
    Results: In chondrocytes, type II collagen expression was significantly enhanced in the presence of 3 μM carnosol (p = 0.008). MMP-3, IL-6, NO production and ADAMTS-4 expression were down-regulated in a concentration-dependent manner by carnosol (p<0.01). TIMP-1 production was slightly increased at 3 μM (p = 0.02) and ADAMTS-5 expression was decreased from 0.2 to 9 μM carnosol (p<0.05). IL-6 and PGE2 production was reduced in the presence of carnosol in both SC and NSC osteoblasts while alkaline phosphatase activity was not changed. In co-culture experiments preincubation of NSC and SC osteoblasts wih carnosol resulted in similar effects to incubation with anti-IL-6 antibody, namely a significant increase in aggrecan and decrease in MMP-3, ADAMTS-4 and -5 gene expression by chondrocytes.
    Conclusions: Carnosol showed potent inhibition of pro-inflammatory and catabolic mediators of cartilage breakdown in chondrocytes. Inhibition of matrix degradation and enhancement of formation was observed in chondrocytes cocultured with subchondral osteoblasts preincubated with carnosol indicating a cross-talk between these two cellular compartments, potentially mediated via inhibition of IL-6 in osteoblasts as similar results were obtained with anti-IL-6 antibody.
    MeSH term(s) Aggrecans/immunology ; Anti-Inflammatory Agents/pharmacology ; Cell Survival/drug effects ; Cells, Cultured ; Chondrocytes/drug effects ; Chondrocytes/immunology ; Chondrocytes/pathology ; Coculture Techniques ; Dinoprostone/immunology ; Diterpenes, Abietane/pharmacology ; Humans ; Interleukin-6/immunology ; Matrix Metalloproteinase 3/immunology ; Osteoarthritis/drug therapy ; Osteoarthritis/immunology ; Osteoarthritis/pathology ; Osteoblasts/drug effects ; Osteoblasts/immunology ; Osteoblasts/pathology ; Tissue Inhibitor of Metalloproteinase-1/immunology
    Chemical Substances Aggrecans ; Anti-Inflammatory Agents ; Diterpenes, Abietane ; Interleukin-6 ; Tissue Inhibitor of Metalloproteinase-1 ; carnosol (483O455CKD) ; MMP3 protein, human (EC 3.4.24.17) ; Matrix Metalloproteinase 3 (EC 3.4.24.17) ; Dinoprostone (K7Q1JQR04M)
    Language English
    Publishing date 2015
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0136118
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article: Animal models of osteoarthritis: lessons learned while seeking the "Holy Grail".

    Ameye, Laurent G / Young, Marian F

    Current opinion in rheumatology

    2006  Volume 18, Issue 5, Page(s) 537–547

    Abstract: Purpose of review: Difficulties in studying osteoarthritis in humans that stem from both the low sensitivity of diagnostic tools and the low availability of diseased tissues explain why research on animal models remains highly dynamic. This review will ... ...

    Abstract Purpose of review: Difficulties in studying osteoarthritis in humans that stem from both the low sensitivity of diagnostic tools and the low availability of diseased tissues explain why research on animal models remains highly dynamic. This review will summarize the recent advances in this field.
    Recent findings: With regard to the etiology of osteoarthritis, synovial macrophages mediate osteophyte formation, whereas increased ligament laxity could be responsible for spontaneous osteoarthritis in guinea pigs. The concomitant changes in subchondral bone and cartilage reported in several models, and the structure-modifying effects of some bone inhibitors have confirmed the importance of bone in osteoarthritis. With regard to cartilage pathobiology, ADAMTS-5 is the major aggrecanase responsible for cartilage destruction, whereas inadequate control of oxidative stress and decreased expression of transforming growth factor-beta receptors could predispose to osteoarthritis. New models include a postmenopausal rat model, the groove model and a joint-specific bone morphogenetic receptor-deficient mouse. The iodoacetate model was also validated as the first pain model of osteoarthritis.
    Summary: In view of the multiple animal models available, there is a need to reach a consensus on one or several gold standard animal model(s). New studies indicate that important differences in therapeutic response exist between young and old animals, and between spontaneous and surgical models, suggesting that not all models are adequate models of osteoarthritis.
    MeSH term(s) ADAM Proteins/metabolism ; ADAMTS5 Protein ; Animals ; Bone and Bones/metabolism ; Bone and Bones/pathology ; Cartilage/metabolism ; Cartilage/pathology ; Disease Models, Animal ; Gene Expression Regulation ; Guinea Pigs ; Humans ; Mice ; Mice, Transgenic ; Osteoarthritis/diagnosis ; Osteoarthritis/etiology ; Osteoarthritis/metabolism ; Osteoarthritis/pathology ; Osteoarthritis/therapy ; Oxidative Stress ; Pain/chemically induced ; Pain/metabolism ; Pain/pathology ; Pain Management ; Rats ; Transforming Growth Factor beta/biosynthesis
    Chemical Substances Transforming Growth Factor beta ; ADAM Proteins (EC 3.4.24.-) ; ADAMTS5 Protein (EC 3.4.24.-) ; ADAMTS5 protein, human (EC 3.4.24.-)
    Language English
    Publishing date 2006-09
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 1045317-9
    ISSN 1531-6963 ; 1040-8711
    ISSN (online) 1531-6963
    ISSN 1040-8711
    DOI 10.1097/01.bor.0000240369.39713.af
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Effects on Fatty Acid Metabolism of a New Powdered Human Milk Fortifier Containing Medium-Chain Triacylglycerols and Docosahexaenoic Acid in Preterm Infants.

    Billeaud, Claude / Boué-Vaysse, Carole / Couëdelo, Leslie / Steenhout, Philippe / Jaeger, Jonathan / Cruz-Hernandez, Cristina / Ameye, Laurent / Rigo, Jacques / Picaud, Jean-Charles / Saliba, Elie / Hays, Nicholas P / Destaillats, Frédéric

    Nutrients

    2018  Volume 10, Issue 6

    Abstract: Preterm infants require fortification of human milk (HM) with essential fatty acids (FA) to ensure adequate post-natal development. As part of a larger randomized controlled study, we investigated FA metabolism in a subset of 47 clinically stable preterm ...

    Abstract Preterm infants require fortification of human milk (HM) with essential fatty acids (FA) to ensure adequate post-natal development. As part of a larger randomized controlled study, we investigated FA metabolism in a subset of 47 clinically stable preterm infants (birth weight ≤1500 g or gestational age ≤32 weeks). Infants were randomized to receive HM supplemented with either a new HM fortifier (nHMF;
    MeSH term(s) Arachidonic Acid/blood ; Dietary Carbohydrates/administration & dosage ; Dietary Fats/administration & dosage ; Dietary Proteins/administration & dosage ; Docosahexaenoic Acids/administration & dosage ; Docosahexaenoic Acids/blood ; Double-Blind Method ; Erythrocytes/metabolism ; Fatty Acids, Essential/administration & dosage ; Fatty Acids, Essential/blood ; Fatty Acids, Monounsaturated/blood ; Female ; Food, Fortified/analysis ; Humans ; Infant Formula/chemistry ; Infant, Newborn ; Infant, Premature/blood ; Infant, Premature/growth & development ; Linoleic Acid/administration & dosage ; Linoleic Acid/blood ; Lipid Metabolism ; Male ; Milk, Human ; Phosphatidylcholines/blood ; Phosphatidylethanolamines/blood ; Powders ; Triglycerides/administration & dosage ; Triglycerides/blood ; alpha-Linolenic Acid/administration & dosage ; alpha-Linolenic Acid/blood
    Chemical Substances Dietary Carbohydrates ; Dietary Fats ; Dietary Proteins ; Fatty Acids, Essential ; Fatty Acids, Monounsaturated ; Phosphatidylcholines ; Phosphatidylethanolamines ; Powders ; Triglycerides ; alpha-Linolenic Acid (0RBV727H71) ; Docosahexaenoic Acids (25167-62-8) ; Arachidonic Acid (27YG812J1I) ; phosphatidylethanolamine (39382-08-6) ; Linoleic Acid (9KJL21T0QJ)
    Language English
    Publishing date 2018-05-29
    Publishing country Switzerland
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu10060690
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: Carnosol Inhibits Pro-Inflammatory and Catabolic Mediators of Cartilage Breakdown in Human Osteoarthritic Chondrocytes and Mediates Cross-Talk between Subchondral Bone Osteoblasts and Chondrocytes.

    Christelle Sanchez / Marie-Noëlle Horcajada / Fanny Membrez Scalfo / Laurent Ameye / Elizabeth Offord / Yves Henrotin

    PLoS ONE, Vol 10, Iss 8, p e

    2015  Volume 0136118

    Abstract: The aim of this work was to evaluate the effects of carnosol, a rosemary polyphenol, on pro-inflammatory and catabolic mediators of cartilage breakdown in chondrocytes and via bone-cartilage crosstalk.Osteoarthritic (OA) human chondrocytes were cultured ... ...

    Abstract The aim of this work was to evaluate the effects of carnosol, a rosemary polyphenol, on pro-inflammatory and catabolic mediators of cartilage breakdown in chondrocytes and via bone-cartilage crosstalk.Osteoarthritic (OA) human chondrocytes were cultured in alginate beads for 4 days in presence or absence of carnosol (6 nM to 9 μM). The production of aggrecan, matrix metalloproteinase (MMP)-3, tissue inhibitor of metalloproteinase (TIMP)-1, interleukin (IL)-6 and nitric oxide (NO) and the expression of type II collagen and ADAMTS-4 and -5 were analyzed. Human osteoblasts from sclerotic (SC) or non-sclerotic (NSC) subchondral bone were cultured for 3 days in presence or absence of carnosol before co-culture with chondrocytes. Chondrocyte gene expression was analyzed after 4 days of co-culture.In chondrocytes, type II collagen expression was significantly enhanced in the presence of 3 μM carnosol (p = 0.008). MMP-3, IL-6, NO production and ADAMTS-4 expression were down-regulated in a concentration-dependent manner by carnosol (p<0.01). TIMP-1 production was slightly increased at 3 μM (p = 0.02) and ADAMTS-5 expression was decreased from 0.2 to 9 μM carnosol (p<0.05). IL-6 and PGE2 production was reduced in the presence of carnosol in both SC and NSC osteoblasts while alkaline phosphatase activity was not changed. In co-culture experiments preincubation of NSC and SC osteoblasts wih carnosol resulted in similar effects to incubation with anti-IL-6 antibody, namely a significant increase in aggrecan and decrease in MMP-3, ADAMTS-4 and -5 gene expression by chondrocytes.Carnosol showed potent inhibition of pro-inflammatory and catabolic mediators of cartilage breakdown in chondrocytes. Inhibition of matrix degradation and enhancement of formation was observed in chondrocytes cocultured with subchondral osteoblasts preincubated with carnosol indicating a cross-talk between these two cellular compartments, potentially mediated via inhibition of IL-6 in osteoblasts as similar results were obtained with anti-IL-6 ...
    Keywords Medicine ; R ; Science ; Q
    Subject code 616
    Language English
    Publishing date 2015-01-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  9. Article: Mice deficient in small leucine-rich proteoglycans: novel in vivo models for osteoporosis, osteoarthritis, Ehlers-Danlos syndrome, muscular dystrophy, and corneal diseases.

    Ameye, Laurent / Young, Marian F

    Glycobiology

    2002  Volume 12, Issue 9, Page(s) 107R–16R

    Abstract: Small leucine-rich proteoglycans (SLRPs) are extracellular molecules that bind to TGFbetas and collagens and other matrix molecules. In vitro, SLRPs were shown to regulate collagen fibrillogenesis, a process essential in development, tissue repair, and ... ...

    Abstract Small leucine-rich proteoglycans (SLRPs) are extracellular molecules that bind to TGFbetas and collagens and other matrix molecules. In vitro, SLRPs were shown to regulate collagen fibrillogenesis, a process essential in development, tissue repair, and metastasis. To better understand their functions in vivo, mice deficient in one or two of the four most prominent and widely expressed SLRPs (biglycan, decorin, fibromodulin, and lumican) were recently generated. All four SLRP deficiencies result in the formation of abnormal collagen fibrils. Taken together, the collagen phenotypes demonstrate a cooperative, sequential, timely orchestrated action of the SLRPs that altogether shape the architecture and mechanical properties of the collagen matrix. In addition, SLRP-deficient mice develop a wide array of diseases (osteoporosis, osteoarthritis, muscular dystrophy, Ehlers-Danlos syndrome, and corneal diseases), most of them resulting primarily from an abnormal collagen fibrillogenesis. The development of these diseases by SLRP-deficient mice suggests that mutations in SLRPs may be part of undiagnosed predisposing genetic factors for these diseases. Although the distinct phenotypes developed by the different singly deficient mice point to distinct in vivo function for each SLRP, the analysis of the double-deficient mice also demonstrates the existence of rescuing/compensation mechanisms, indicating some functional overlap within the SLRP family.
    MeSH term(s) Animals ; Corneal Diseases/physiopathology ; Ehlers-Danlos Syndrome/physiopathology ; Leucine/chemistry ; Mice ; Mice, Knockout ; Models, Molecular ; Muscular Dystrophies/physiopathology ; Osteoarthritis/physiopathology ; Osteoporosis/physiopathology ; Proteoglycans/chemistry ; Proteoglycans/genetics ; Proteoglycans/physiology
    Chemical Substances Proteoglycans ; Leucine (GMW67QNF9C)
    Language English
    Publishing date 2002-09
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1067689-2
    ISSN 1460-2423 ; 0959-6658
    ISSN (online) 1460-2423
    ISSN 0959-6658
    DOI 10.1093/glycob/cwf065
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article: Correction: Billeaud et al. “Effects on Fatty Acid Metabolism of a New Powdered Human Milk Fortifier Containing Medium-Chain Triacylglycerols and Docosahexaenoic Acid in Preterm Infants” <i>Nutrients</i> 2018, <i>10</i>, 690

    Billeaud, Claude / Ameye, Laurent / Boué-Vaysse, Carole / Couëdelo, Leslie / Cruz-Hernandez, Cristina / Destaillats, Frédéric / Hays, Nicholas P / Jaeger, Jonathan / Picaud, Jean-Charles / Rigo, Jacques / Saliba, Elie / Steenhout, Philippe

    Nutrients. 2019 Mar. 22, v. 11, no. 3

    2019  

    Abstract: The authors wish to make a correction to the published version of their paper [ ... ] ...

    Abstract The authors wish to make a correction to the published version of their paper [...]
    Keywords breast milk ; docosahexaenoic acid ; fatty acid metabolism ; medium chain triacylglycerols ; nutrients ; premature birth
    Language English
    Dates of publication 2019-0322
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    ZDB-ID 2518386-2
    ISSN 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu11030680
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

To top