Jessica M. Lindvall

ORCID: 0000-0002-5042-8481
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About
Contact & Profiles
Research Areas
  • T-cell and B-cell Immunology
  • Chronic Lymphocytic Leukemia Research
  • Genetics, Bioinformatics, and Biomedical Research
  • Immunodeficiency and Autoimmune Disorders
  • Immune Cell Function and Interaction
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Biomedical and Engineering Education
  • DNA Repair Mechanisms
  • Genetics, Aging, and Longevity in Model Organisms
  • Epigenetics and DNA Methylation
  • RNA Research and Splicing
  • Mitochondrial Function and Pathology
  • Gene expression and cancer classification
  • Genomics and Phylogenetic Studies
  • Noise Effects and Management
  • Vehicle Noise and Vibration Control
  • Lymphoma Diagnosis and Treatment
  • CAR-T cell therapy research
  • Cancer-related gene regulation
  • Interdisciplinary Research and Collaboration
  • Social and Educational Sciences
  • Insect symbiosis and bacterial influences
  • Genomics and Chromatin Dynamics
  • Fungal and yeast genetics research
  • RNA modifications and cancer

Science for Life Laboratory
2016-2023

Stockholm University
2016-2022

National Bioinformatics Infrastructure Sweden
2020

Karolinska Institutet
2002-2016

Karolinska University Hospital
2004-2016

Akershus University Hospital
2016

University of Oslo
2007-2013

University of Gothenburg
2013

We sought to determine whether acute resistance exercise (RE)-induced gene expression is modified by RE training. studied the patterns of a select group genes following an bout in naïve and hypertrophying muscle. Thirteen untrained subjects underwent supervised training for 12 wk nondominant arm performed 1 after last program ( training+acute). The dominant was either unexercised control) or subjected same as trained RE). Following training, men (14.8 ± 2.8%; P < 0.05) women (12.6 2.4%;...

10.1152/japplphysiol.01366.2013 article EN Journal of Applied Physiology 2014-01-24

Epigenetic modifications contribute to the etiology of type 2 diabetes.We performed genome-wide methylome and transcriptome analysis in liver from severely obese men with or without diabetes non-obese discover aberrant pathways underlying development insulin resistance. Results were validated by pyrosequencing.We identified hypomethylation genes involved hepatic glycolysis resistance, concomitant increased mRNA expression protein levels. Pyrosequencing revealed CpG-site within ATF-motifs was...

10.1016/j.molmet.2015.12.004 article EN cc-by-nc-nd Molecular Metabolism 2016-01-02

Despite a considerable focus on the adverse effects of silver nanoparticles (AgNPs) in recent years, studies potential long-term AgNPs are scarce. The aim this study was to explore following repeated low-dose, exposure human bronchial epithelial cells. To end, BEAS-2B cell line exposed 1 µg/mL (10 nm) for 6 weeks followed by RNA-sequencing (RNA-Seq) as well genome-wide DNA methylation analysis. transcriptomics analysis showed that substantial number genes (1717) were differentially expressed...

10.1038/s41598-018-25085-5 article EN cc-by Scientific Reports 2018-04-23

Abstract Background Chronic fatigue syndrome (CFS) is a prevalent and disabling condition affecting adolescents. The pathophysiology poorly understood, but immune alterations might be an important component. This study compared whole blood gene expression in adolescent CFS patients healthy controls, explored associations between neuroendocrine markers, markers clinical within the group. Methods (12–18 years old) were recruited nation-wide to single referral center as part of NorCAPITAL...

10.1186/s12967-017-1201-0 article EN cc-by Journal of Translational Medicine 2017-05-11

Abstract Background Innate immune responses are evolutionarily conserved processes that provide crucial protection against invading organisms. Gene activation by potent NF-κB transcription factors is essential both in mammals and Drosophila during infection stress challenges. If not strictly controlled, this defense system can activate autoimmune inflammatory reactions, with deleterious consequences for the organism. Negative regulation to prevent gene healthy organisms, presence of...

10.1186/1741-7007-11-99 article EN cc-by BMC Biology 2013-09-06

Transcription-blocking oxidative DNA damage is believed to contribute aging and underlie activation of stress responses downregulation insulin-like signaling (ILS) in Nucleotide Excision Repair (NER) deficient mice.Here, we present the first quantitative proteomic description Caenorhabditis elegans NER-defective xpa-1 mutant compare proteome transcriptome signatures.Both methods indicated responses, which was substantiated biochemically by a bioenergetic shift involving increased...

10.1093/nar/gkt225 article EN cc-by-nc Nucleic Acids Research 2013-04-10

Abstract T cells expressing the cutaneous lymphocyte antigen (CLA) mediate pathogenic inflammation in atopic dermatitis (AD). The molecular alterations contributing to their dysregulation remain unclear. With aim elucidate putative altered pathways AD we profiled DNA methylation levels and miRNA expression sorted cell populations (CD4 + , CD4 CD45RA naïve, CLA CD8 ) from adult patients healthy controls (HC). Skin homing showed significant differences 40 genes compared HC ( p < 0.05)....

10.1038/s41598-020-74798-z article EN cc-by Scientific Reports 2020-10-22

The cyclin-dependent kinase Cdc28 is the master regulator of cell cycle in Saccharomyces cerevisiae . initiates by activating cell-cycle–specific transcription factors that switch on a transcriptional program during late G1 phase. also has cell-cycle–independent, direct function regulating basal transcription, which does not require its catalytic activity. However, exact role remains poorly understood, and for activity been fully explored. Here we show important transcription. Using...

10.1073/pnas.1200067109 article EN Proceedings of the National Academy of Sciences 2012-06-11

Human-nucleotide-excision repair (NER) deficiency leads to different developmental and segmental progeroid symptoms of which the pathogenesis is only partially understood. To understand biological impact accumulating spontaneous DNA damage, we studied phenotypic consequences DNA-repair in Caenorhabditis elegans. We find that damage accumulation does not decrease adult life span post-mitotic tissue. Surprisingly, loss functional ERCC-1/XPF even further extends long-lived daf-2 mutants, likely...

10.1038/cdd.2013.126 article EN cc-by-nc-nd Cell Death and Differentiation 2013-09-06

Summary Bruton's tyrosine kinase (Btk), a member of the Tec family kinases, plays an important role in differentiation and activation B cells. Mutations affecting Btk cause immunodeficiency both humans mice. In this study we set out to investigate potential Toll‐like receptor 9 (TLR9) production pro‐inflammatory cytokines such as interleukin (IL)‐6, tumour necrosis factor (TNF)‐α IL‐12p40. Our data show that Btk‐deficient cells respond more efficiently CpG‐DNA stimulation, producing...

10.1111/j.1365-2567.2007.02693.x article EN Immunology 2007-08-28

Curriculum development in higher education should follow a formal process. Although the focus curriculum theory is on long-term programs of study, theoretical and practical considerations are also applicable to shorter-form learning experiences (single courses, lessons, or training sessions). With these mind, we discuss here an iterative model design, starting point which (indeed, construction any experience), articulation target outcomes: everything follows from these, including selection...

10.31235/osf.io/7qeht preprint EN 2020-04-03

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a key regulator of serum cholesterol. The possibility that PCSK9 also functions in other pathways needs to be addressed. We have transfected HepG2 cells with mutant D374Y-PCSK9 or control vector. Gene expression signatures were determined using the Affymetrix GeneChip technology, and pattern selected genes was confirmed by quantitative real-time polymerase chain reaction (qRT-PCR). Data normalized analyzed model-based background...

10.1002/jcp.21519 article EN Journal of Cellular Physiology 2008-06-20

Cyclin-dependent kinases (CDKs) control the eukaryotic cell cycle, and a single CDK, Cdc28 (also known as Cdk1), is necessary sufficient for cycle regulation in budding yeast Saccharomyces cerevisiae . regulates cycle-dependent processes such transcription, DNA replication repair, chromosome segregation. To gain further insight into functions of Cdc28, we performed high-throughput chemical-genetic array (CGA) screen aimed at unraveling genetic network CDC28 We identified 107 genes that...

10.1073/pnas.1115885108 article EN Proceedings of the National Academy of Sciences 2011-10-31

The neural crest is a transient embryonic stem cell population. Hypoxia inducible factor (HIF)-2α associated with appearance and aggressiveness in tumors. However, little known about its role normal development.Here, we show that HIF-2α expressed trunk cells of human, murine, avian embryos. Knockdown as well overexpression vivo causes developmental delays, induces proliferation, self-renewal capacity while decreasing the proportion migrate ventrally to sympathoadrenal sites. Reflecting...

10.1002/dvdy.253 article EN cc-by Developmental Dynamics 2020-09-17

ABSTRACT Science, technology, engineering, mathematics, and medicine (STEMM) fields change rapidly are increasingly interdisciplinary. Commonly, STEMM practitioners use short-format training (SFT) such as workshops short courses for upskilling reskilling, but unaddressed challenges limit SFT’s effectiveness inclusiveness. Prior work, including the NSF 2026 Reinventing Scientific Talent proposal, called addressing SFT challenges, a diverse international group of experts in education,...

10.1101/2023.03.10.531570 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2023-03-13

Activation of oxidative stress-responses and downregulation insulin-like signaling (ILS) is seen in Nucleotide Excision Repair (NER) deficient segmental progeroid mice. Evidence suggests that this a survival response to persistent transcription-blocking DNA damage, although the relevant lesions have not been identified. Here we show loss NTH-1, only Base (BER) enzyme known initiate repair damage inC. elegans, restores normal lifespan short-lived NER xpa-1 mutant. Loss NTH-1 leads stress...

10.18632/aging.100127 article EN cc-by Aging 2010-03-29

Developmental dyslexia is the most common learning disorder in children. Problems reading and writing are likely due to a complex interaction of genetic environmental factors, resulting reduced power studies factors underlying developmental dyslexia. Our approach current study was perform exome sequencing affected unaffected individuals within an extended pedigree with familial form We identified two-base mutation, causing p.R229L amino acid substitution centrosomal protein 63 kDa (CEP63),...

10.1007/s00439-015-1602-1 article EN cc-by Human Genetics 2015-09-23

Gut immunity is regulated by intricate and dynamic mechanisms to ensure homeostasis despite a constantly changing microbial environment. Several regulatory factors have been described participate in feedback responses prevent aberrant immune activity. Little is, however, known about how transcriptional programs are directly tuned efficiently adapt host gut tissues the current microbiome. Here we show that POU/Oct gene nubbin (nub) encodes two transcription factor isoforms, Nub-PB Nub-PD,...

10.1371/journal.ppat.1006936 article EN cc-by PLoS Pathogens 2018-03-02

As the life sciences have become more data intensive, pressure to incorporate requisite training into life-science education and programs has increased. To facilitate curriculum development, various sets of (bio)informatics competencies been articulated; however, these proved difficult implement in practice. Addressing this issue, we created a curriculum-design -evaluation tool support development specific Knowledge, Skills Abilities (KSAs) that reflect scientific method promote both...

10.1371/journal.pone.0225256 article EN cc-by PLoS ONE 2019-11-26
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