Search Results - "Ingvast, S."
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Characterization of human organ donors testing positive for type 1 diabetes‐associated autoantibodies
Published in Clinical and experimental immunology (01-12-2015)“…Summary In this study we aim to describe the characteristics of non‐diabetic organ donors with circulating diabetes‐associated autoantibodies collected within…”
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2
New Alzheimer’s disease locus on chromosome 8
Published in Journal of medical genetics (01-12-2006)“…Background: Family history is one of the most consistent risk factors for dementia. Therefore, analysis of families with a distinct inheritance pattern of…”
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3
Noninvasive PET Detection of CD69-Positive Immune Cells Before Signs of Clinical Disease in Inflammatory Arthritis
Published in Journal of Nuclear Medicine (01-02-2024)“…Rheumatoid arthritis (RA) is the most common inflammatory joint disease, and early diagnosis is key for effective disease management. CD69 is one of the…”
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4
Characterization of host defense molecules in the human pancreas
Published in Islets (04-07-2019)“…The gut microbiota can play a role in pancreatitis and, likely, in the development of type 1 diabetes (T1D). Anti-microbial peptides and secretory proteins are…”
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5
Protein Kinase R Is Constitutively Expressed in the Human Pancreas
Published in The journal of histochemistry and cytochemistry (01-02-2019)“…Summary Viral infection of the insulin-producing cells in the pancreas has been proposed in the etiology of type 1 diabetes. Protein kinase R (PKR) is a…”
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Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene
Published in Ophthalmic genetics (1999)“…Objective: To examine the clinical phenotype of three Swedish families with Best's vitelliform macular dystrophy (BMD) and three different mutations in the…”
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Further Evidence for an Association of ABCR Alleles with Age-Related Macular Degeneration
Published in American journal of human genetics (01-08-2000)“…Age-related macular degeneration (AMD) accounts for >50% of the registered visual disability among North American and Western European populations and has been…”
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The mutation spectrum of the bestrophin protein : functional implications
Published in Human genetics (01-05-1999)“…Best's macular dystrophy (BMD), also known as vitelliform macular degeneration type 2 (VMD2; OMIM 153700), is an autosomal dominant form of macular…”
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The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe
Published in European journal of human genetics : EJHG (01-03-2002)“…Inherited retinal dystrophies represent the most important cause of vision impairment in adolescence, affecting approximately 1 out of 3000 individuals…”
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