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  • 1. Choi, M. J.
    et al.
    Jung, S. -B
    Lee, S. E.
    Kang, S. G.
    Lee, J. H.
    Ryu, M. J.
    Chung, H. K.
    Chang, J. Y.
    Kim, Y. K.
    Hong, H. J.
    Kim, H.
    Kim, H. J.
    Lee, C. -H
    Mardinoglu, Adil
    KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Systems Biology. Kings Coll London, Fac Dent Oral & Craniofacial Sci, Ctr Host Microbiome Interact, London, England.
    Yi, H. -S
    Shong, M.
    An adipocyte-specific defect in oxidative phosphorylation increases systemic energy expenditure and protects against diet-induced obesity in mouse models2020In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428Article in journal (Refereed)
    Abstract [en]

    Aims/hypothesis: Mitochondrial oxidative phosphorylation (OxPhos) is essential for energy production and survival. However, the tissue-specific and systemic metabolic effects of OxPhos function in adipocytes remain incompletely understood. Methods: We used adipocyte-specific Crif1 (also known as Gadd45gip1) knockout (AdKO) mice with decreased adipocyte OxPhos function. AdKO mice fed a normal chow or high-fat diet were evaluated for glucose homeostasis, weight gain and energy expenditure (EE). RNA sequencing of adipose tissues was used to identify the key mitokines affected in AdKO mice, which included fibroblast growth factor 21 (FGF21) and growth differentiation factor 15 (GDF15). For in vitro analysis, doxycycline was used to pharmacologically decrease OxPhos in 3T3L1 adipocytes. To identify the effects of GDF15 and FGF21 on the metabolic phenotype of AdKO mice, we generated AdKO mice with global Gdf15 knockout (AdGKO) or global Fgf21 knockout (AdFKO). Results: Under high-fat diet conditions, AdKO mice were resistant to weight gain and exhibited higher EE and improved glucose tolerance. In vitro pharmacological and in vivo genetic inhibition of OxPhos in adipocytes significantly upregulated mitochondrial unfolded protein response-related genes and secretion of mitokines such as GDF15 and FGF21. We evaluated the metabolic phenotypes of AdGKO and AdFKO mice, revealing that GDF15 and FGF21 differentially regulated energy homeostasis in AdKO mice. Both mitokines had beneficial effects on obesity and insulin resistance in the context of decreased adipocyte OxPhos, but only GDF15 regulated EE in AdKO mice. Conclusions/interpretation: The present study demonstrated that the adipose tissue adaptive mitochondrial stress response affected systemic energy homeostasis via cell-autonomous and non-cell-autonomous pathways. We identified novel roles for adipose OxPhos and adipo-mitokines in the regulation of systemic glucose homeostasis and EE, which facilitated adaptation of an organism to local mitochondrial stress.

  • 2. Dawed, A. Y.
    et al.
    Mari, A.
    McDonald, T. J.
    Hong, Mun-Gwan
    KTH, Centres, Science for Life Laboratory, SciLifeLab.
    Sharma, S.
    Robertson, N. R.
    Mahajan, A.
    Walker, M.
    Gough, S.
    Zhou, K.
    Forgie, I.
    Ruetten, H.
    Jones, A. G.
    Pearson, E. R.
    GLP-1 receptor variants markedly differentiate glycaemic response to GLP-1 receptor agonists: a DIRECT study2017In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 60, p. S393-S393Article in journal (Refereed)
  • 3.
    Ferrannini, G.
    et al.
    Karolinska Inst, Med, Stockholm, Sweden.;Södertälje Hosp, Stockholm, Sweden..
    Fortin, E.
    Karolinska Inst, Med, Stockholm, Sweden..
    Mellbin, L.
    Karolinska Inst, Med, Stockholm, Sweden.;Karolinska Univ Hosp, Stockholm, Sweden..
    Norhammar, A.
    Karolinska Inst, Med, Stockholm, Sweden.;Capio St Gorans Hosp, Stockholm, Sweden..
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Real Estate and Construction Management, Real Estate Economics and Finance. Karolinska Inst, Stockholm, Sweden..
    Smetana, S.
    Ferrannini, E.
    CNR, Pisa, Italy..
    Ryden, L.
    Karolinska Inst, Med, Stockholm, Sweden..
    Empagliflozin improves insulin sensitivity in patients with a recent coronary syndrome and newly detected dysglycaemia2023In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 66, no SUPPL 1, p. S243-S244Article in journal (Other academic)
  • 4.
    Fortin, E.
    et al.
    Karolinska Inst, Med K2, Stockholm, Sweden..
    Campi, B.
    CNRS, Inst Clin Physiol, Pisa, Italy..
    Ferrannini, E.
    CNRS, Inst Clin Physiol, Pisa, Italy..
    Mari, A.
    CNRS, Inst Neurosci, Padua, Italy..
    Mellbin, L.
    Karolinska Inst, Med K2, Stockholm, Sweden..
    Norhammar, A.
    Karolinska Inst, Med K2, Stockholm, Sweden..
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Real Estate and Construction Management, Real Estate Economics and Finance.
    Ryden, L.
    Karolinska Inst, Med K2, Stockholm, Sweden..
    Saba, A.
    Univ Pisa, Dept Pathol, Pisa, Italy..
    Ferrannini, G.
    Karolinska Inst, Med K2, Stockholm, Sweden..
    High mannose correlates with surrogate indexes of insulin resistance and predicts cardiovascular events independently of glycaemic status and traditional risk factors2023In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 66, no SUPPL 1, p. S493-S493Article in journal (Other academic)
  • 5.
    Fortin, E.
    et al.
    Karolinska Inst, Dept Med K2, Stockholm, Sweden..
    Ferrannini, G.
    Karolinska Inst, Dept Med K2, Stockholm, Sweden..
    Campi, B.
    CNR, Inst Clin Physiol, Pisa, Italy..
    Mellbin, L.
    Karolinska Inst, Dept Med K2, Stockholm, Sweden..
    Norhammar, A.
    Karolinska Inst, Dept Med K2, Stockholm, Sweden..
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Centres, Centre for Traffic Research, CTR.
    Saba, A.
    Univ Pisa, Dept Surg Med Mol & Crit Area Pathol, Lab Biochem, Pisa, Italy..
    Ferrannini, E.
    CNR, Inst Clin Physiol, Pisa, Italy..
    Ryden, L.
    Karolinska Inst, Dept Med K2, Stockholm, Sweden..
    Plasma mannose and a first myocardial infarction: associations according to glycaemic state2022In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 65, no SUPPL 1, p. S412-S413Article in journal (Other academic)
  • 6. Heinonen, Sini
    et al.
    Muniandy, Maheswary
    Buzkova, Jana
    Mardinoglu, Adil
    KTH, School of Biotechnology (BIO), Proteomics and Nanobiotechnology. KTH, Centres, Science for Life Laboratory, SciLifeLab. Chalmers University of Technology, Sweden.
    Rodriguez, Amaia
    Fruhbeck, Gema
    Hakkarainen, Antti
    Lundbom, Jesper
    Lundbom, Nina
    Kaprio, Jaakko
    Rissanen, Aila
    Pietilainen, Kirsi H.
    Mitochondria-related transcriptional signature is downregulated in adipocytes in obesity: a study of young healthy MZ twins2017In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 60, no 1, p. 169-181Article in journal (Refereed)
    Abstract [en]

    Low mitochondrial activity in adipose tissue is suggested to be an underlying factor in obesity and its metabolic complications. We aimed to find out whether mitochondrial measures are downregulated in obesity also in isolated adipocytes. We studied young adult monozygotic (MZ) twin pairs discordant (n = 14, intrapair difference Delta BMI ae<yen> 3 kg/m(2)) and concordant (n = 5, Delta BMI < 3 kg/m(2)) for BMI, identified from ten birth cohorts of 22- to 36-year-old Finnish twins. Abdominal body fat distribution (MRI), liver fat content (magnetic resonance spectroscopy), insulin sensitivity (OGTT), high-sensitivity C-reactive protein, serum lipids and adipokines were measured. Subcutaneous abdominal adipose tissue biopsies were obtained to analyse the transcriptomics patterns of the isolated adipocytes as well as of the whole adipose tissue. Mitochondrial DNA transcript levels in adipocytes were measured by quantitative real-time PCR. Western blots of oxidative phosphorylation (OXPHOS) protein levels in adipocytes were performed in obese and lean unrelated individuals. The heavier (BMI 29.9 +/- 1.0 kg/m(2)) co-twins of the discordant twin pairs had more subcutaneous, intra-abdominal and liver fat and were more insulin resistant (p < 0.01 for all measures) than the lighter (24.1 +/- 0.9 kg/m(2)) co-twins. Altogether, 2538 genes in adipocytes and 2135 in adipose tissue were significantly differentially expressed (nominal p < 0.05) between the co-twins. Pathway analysis of these transcripts in both isolated adipocytes and adipose tissue revealed that the heavier co-twins displayed reduced expression of genes relating to mitochondrial pathways, a result that was replicated when analysing the pathways behind the most consistently downregulated genes in the heavier co-twins (in at least 12 out of 14 pairs). Consistently upregulated genes in adipocytes were related to inflammation. We confirmed that mitochondrial DNA transcript levels (12S RNA, 16S RNA, COX1, ND5, CYTB), expression of mitochondrial ribosomal protein transcripts and a major mitochondrial regulator PGC-1 alpha (also known as PPARGC1A) were reduced in the heavier co-twins' adipocytes (p < 0.05). OXPHOS protein levels of complexes I and III in adipocytes were lower in obese than in lean individuals. Subcutaneous abdominal adipocytes in obesity show global expressional downregulation of oxidative pathways, mitochondrial transcripts and OXPHOS protein levels and upregulation of inflammatory pathways. The datasets analysed and generated during the current study are available in the figshare repository.

  • 7. Johansson, I.
    et al.
    Dahlstrom, U.
    Edner, M.
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Transport Science, Transport Planning, Economics and Engineering.
    Ryden, L.
    Norhammar, A.
    Glycosylated haemoglobin predicts mortality in patients with heart failure and unknown diabetes: insights from the Swedish Heart Failure registry (SwedeHF)2016In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 59, p. S532-S532Article in journal (Refereed)
  • 8. Johansson, I.
    et al.
    Edner, M.
    Ryden, L.
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Centres, Centre for Traffic Research, CTR.
    Dahlstrom, U.
    Norhammar, A.
    Impact of diabetes mellitus on long-term prognosis in patients with preserved heart failure: a report from the Swedish Heart Failure Registry (S-HFR)2014In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 57, p. S25-S25Article in journal (Other academic)
  • 9. Koivula, R. W.
    et al.
    Atabaki-Pasdar, N.
    Giordano, G. N.
    White, T.
    Adamski, J.
    Bell, J. D.
    Beulens, J.
    Brage, S.
    Brunak, S.
    De Masi, F.
    Dermitzakis, E. T.
    Forgie, I. M.
    Frost, G.
    Hansen, T.
    Hansen, T. H.
    Hattersley, A.
    Kokkola, T.
    Kurbasic, A.
    Laakso, M.
    Mari, A.
    McDonald, T. J.
    Pedersen, O.
    Rutters, F.
    Schwenk, Jochen M.
    KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics.
    Teare, H. J. A.
    Thomas, E. L.
    Vinuela, A.
    Mahajan, A.
    McCarthy, M. I.
    Ruetten, H.
    Walker, M.
    Pearson, E.
    Pavo, I.
    Franks, P. W.
    Consortium, for the IMI DIRECT
    The role of physical activity in metabolic homeostasis before and after the onset of type 2 diabetes: an IMI DIRECT study2020In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 63, no 4, p. 744-756Article in journal (Refereed)
    Abstract [en]

    Aims/hypothesis: It is well established that physical activity, abdominal ectopic fat and glycaemic regulation are related but the underlying structure of these relationships is unclear. The previously proposed twin-cycle hypothesis (TC) provides a mechanistic basis for impairment in glycaemic control through the interactions of substrate availability, substrate metabolism and abdominal ectopic fat accumulation. Here, we hypothesise that the effect of physical activity in glucose regulation is mediated by the twin-cycle. We aimed to examine this notion in the Innovative Medicines Initiative Diabetes Research on Patient Stratification (IMI DIRECT) Consortium cohorts comprised of participants with normal or impaired glucose regulation (cohort 1: N ≤ 920) or with recently diagnosed type 2 diabetes (cohort 2: N ≤ 435). Methods: We defined a structural equation model that describes the TC and fitted this within the IMI DIRECT dataset. A second model, twin-cycle plus physical activity (TC-PA), to assess the extent to which the effects of physical activity in glycaemic regulation are mediated by components in the twin-cycle, was also fitted. Beta cell function, insulin sensitivity and glycaemic control were modelled from frequently sampled 75 g OGTTs (fsOGTTs) and mixed-meal tolerance tests (MMTTs) in participants without and with diabetes, respectively. Abdominal fat distribution was assessed using MRI, and physical activity through wrist-worn triaxial accelerometry. Results are presented as standardised beta coefficients, SE and p values, respectively. Results: The TC and TC-PA models showed better fit than null models (TC: χ2 = 242, p = 0.004 and χ2 = 63, p = 0.001 in cohort 1 and 2, respectively; TC-PA: χ2 = 180, p = 0.041 and χ2 = 60, p = 0.008 in cohort 1 and 2, respectively). The association of physical activity with glycaemic control was primarily mediated by variables in the liver fat cycle. Conclusions/interpretation: These analyses partially support the mechanisms proposed in the twin-cycle model and highlight mechanistic pathways through which insulin sensitivity and liver fat mediate the association between physical activity and glycaemic control.

  • 10.
    Koivula, Robert W.
    et al.
    Lund Univ, Skane Univ Hosp Malmo, Genet & Mol Epidemiol Unit, Dept Clin Sci,Diabet Ctr,CRC, Bldg 91,Level 10,Jan Waldenstroms Gata 35, SE-20502 Malmo, Sweden.;Univ Oxford, Radcliffe Dept Med, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England..
    Schwenk, Jochen M.
    KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science. KTH Royal Inst Technol, Sch Engn Sci Chem Biotechnol & Hlth, Sci Life Lab, Stockholm, Sweden..
    Franks, Paul W.
    Lund Univ, Skane Univ Hosp Malmo, Genet & Mol Epidemiol Unit, Dept Clin Sci,Diabet Ctr,CRC, Bldg 91,Level 10,Jan Waldenstroms Gata 35, SE-20502 Malmo, Sweden.;Univ Oxford, Radcliffe Dept Med, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England.;Harvard Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA.;Umea Univ, Sect Med, Dept Publ Hlth & Clin Med, Umea, Sweden..
    Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: descriptive characteristics of the epidemiological studies within the IMI DIRECT Consortium2019In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 62, no 9, p. 1601-1615Article in journal (Refereed)
    Abstract [en]

    Here, we describe the characteristics of the Innovative Medicines Initiative (IMI) Diabetes Research on Patient Stratification (DIRECT) epidemiological cohorts at baseline and follow-up examinations (18, 36 and 48 months of follow-up). Methods From a sampling frame of 24,682 adults of European ancestry enrolled in population-based cohorts across Europe, participants at varying risk of glycaemic deterioration were identified using a risk prediction algorithm (based on age, BMI, waist circumference, use of antihypertensive medication, smoking status and parental history of type 2 diabetes) and enrolled into a prospective cohort study (n = 2127) (cohort 1, prediabetes risk). We also recruited people from clinical registries with type 2 diabetes diagnosed 6-24 months previously (n = 789) into a second cohort study (cohort 2, diabetes). Follow-up examinations took place at similar to 18 months (both cohorts) and at similar to 48 months (cohort 1) or similar to 36 months (cohort 2) after baseline examinations. The cohorts were studied in parallel using matched protocols across seven clinical centres in northern Europe. Results Using ADA 2011 glycaemic categories, 33% (n = 693) of cohort 1 (prediabetes risk) had normal glucose regulation and 67% (n = 1419) had impaired glucose regulation. Seventy-six per cent of participants in cohort 1 was male. Cohort 1 participants had the following characteristics (mean +/- SD) at baseline: age 62 (6.2) years; BMI 27.9 (4.0) kg/m(2); fasting glucose 5.7 (0.6) mmol/l; 2 h glucose 5.9 (1.6) mmol/l. At the final follow-up examination the participants' clinical characteristics were as follows: fasting glucose 6.0 (0.6) mmol/l; 2 h OGTT glucose 6.5 (2.0) mmol/l. In cohort 2 (diabetes), 66% (n = 517) were treated by lifestyle modification and 34% (n = 272) were treated with metformin plus lifestyle modification at enrolment. Fifty-eight per cent of participants in cohort 2 was male. Cohort 2 participants had the following characteristics at baseline: age 62 (8.1) years; BMI 30.5 (5.0) kg/m(2); fasting glucose 7.2 (1.4) mmol/l; 2 h glucose 8.6 (2.8) mmol/l. At the final follow-up examination, the participants' clinical characteristics were as follows: fasting glucose 7.9 (2.0) mmol/l; 2 h mixed-meal tolerance test glucose 9.9 (3.4) mmol/l. Conclusions/interpretation The IMI DIRECT cohorts are intensely characterised, with a wide-variety of metabolically relevant measures assessed prospectively. We anticipate that the cohorts, made available through managed access, will provide a powerful resource for biomarker discovery, multivariate aetiological analyses and reclassification of patients for the prevention and treatment of type 2 diabetes.

  • 11. Norhammar, A.
    et al.
    Johansson, I.
    Edner, M.
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Centres, Centre for Traffic Research, CTR.
    Dahlstrom, U.
    Ryden, L.
    Impact of diabetes mellitus on long-term prognosis in patients with ischaemic heart failure: a report from the Swedish Heart Failure Registry (S-HFR)2014In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 57, p. S24-S25Article in journal (Other academic)
  • 12. Norhammar, A.
    et al.
    Kjellstrom, B.
    Habib, N.
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Transport Science, Transport Planning, Economics and Engineering.
    Gustafsson, A.
    Karolinska Inst, Dent Med, Stockholm, Sweden..
    Ryden, L.
    Karolinska Inst, Dept Med, Cardiol Unit, Karolinska Univ Hosp, Stockholm, Sweden..
    Previously unknown glucose abnormalities are common in individuals with periodontitis, especially in those with a previous myocardial infarction2015In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 58, p. S564-S565Article in journal (Other academic)
  • 13.
    Riccio, A.
    et al.
    Sapienza Univ Rome, Dept Clin & Mol Med, Rome, Italy..
    Mellbin, L.
    Karolinska Inst, Dept Med Solna, Stockholm, Sweden.;Karolinska Univ Hosp, Heart Vasc & Neuro Theme, Stockholm, Sweden..
    Norhammar, A.
    Karolinska Inst, Dept Med Solna, Stockholm, Sweden.;Capio St Gorans Hosp, Stockholm, Sweden..
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Real Estate and Construction Management, Real Estate Economics and Finance. Karolinska Inst, Dept Med Solna, Stockholm, Sweden..
    Ryden, L.
    Karolinska Inst, Dept Med Solna, Stockholm, Sweden.;Karolinska Univ Hosp, Heart Vasc & Neuro Theme, Stockholm, Sweden..
    Sesti, G.
    Sapienza Univ Rome, Dept Clin & Mol Med, Rome, Italy..
    Ferrannini, G.
    Karolinska Inst, Dept Med Solna, Stockholm, Sweden..
    Sex differences in the association between insulin resistance indexes and myocardial infarction in individuals with different glycaemic states2023In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 66, no SUPPL 1, p. S247-S247Article in journal (Other academic)
  • 14.
    Rossi, C.
    et al.
    CNR, Inst Neurosci, Padua, Italy..
    Vinuela, A.
    Newcastle Univ, Biosci Inst, Newcastle, NSW, Australia..
    Pearson, E. R.
    Univ Dundee, Populat Hlth & Gen Sch Med, Dundee, Scotland..
    Schwenk, Jochen M.
    KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics. KTH Royal Inst Technol, Sci Life Lab, Stockholm, Sweden..
    Mari, A.
    CNR, Inst Neurosci, Padua, Italy..
    Bizzotto, R.
    CNR, Inst Neurosci, Padua, Italy..
    Association between dynamics of circulating proteins and of beta cell function in type 2 diabetes: an IMI DIRECT study2023In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 66, no SUPPL 1, p. S137-S138Article in journal (Other academic)
  • 15.
    Thomas, Cecilia Engel
    et al.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics. KTH, Centres, Science for Life Laboratory, SciLifeLab.
    Häussler, Ragna S.
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics. KTH, Centres, Science for Life Laboratory, SciLifeLab.
    Hong, Mun-Gwan
    KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics.
    Raverdy, V.
    Ctr Hosp Reg Univ Lille 2, Lille, France..
    Dale, Matilda
    KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics. KTH, Centres, Science for Life Laboratory, SciLifeLab.
    Vinuela, A.
    Univ Geneva, Dept Genet Med & Dev, Sch Med, Geneva, Switzerland..
    Canouil, M.
    Univ Lille, CNRS, Inst Pasteur Lille, Lille, France..
    Dermitzakis, E. T.
    Univ Geneva, Dept Genet Med & Dev, Sch Med, Geneva, Switzerland..
    Froguel, P.
    Univ Lille, CNRS, Inst Pasteur Lille, Lille, France..
    Brunak, S.
    Tech Univ Denmark, Dept Bio & Hlth Informat, Lyngby, Denmark..
    Pattou, F.
    Ctr Hosp Reg Univ Lille 2, Lille, France..
    Schwenk, Jochen M.
    KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Affinity Proteomics.
    Individual effects of gastric bypass surgery on longitudinal blood protein profiles: an IMI DIRECT study2019In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 62, p. S271-S271Article in journal (Other academic)
  • 16. Wang, A.
    et al.
    Arver, S.
    Flanagan, J.
    Mellbin, L. G.
    Gyberg, V.
    Malmberg, K.
    Norhammar, A.
    Näsman, Per
    KTH, School of Architecture and the Built Environment (ABE), Transport Science, Transport Planning, Economics and Engineering.
    Ritsinger, V.
    Ryden, L.
    Testosterone in patients with acute myocardial infarction and glucose abnormalities and in matched controls: a report from the GAMI study2015In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 58, p. S556-S557Article in journal (Other academic)
1 - 16 of 16
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