1. Nybogatan 17, 273 30 Tomelilla
Sweden
Tel: +46 (0)417 10373
Mobile: +46 (0)730 510373
Email: Mattias.Gustafsson@tomelilla.nu
CURRICULUM VITAE
Mattias Gustafsson
SUMMARY
I’m 43 years of age, got a Ph.D. in microbiology from Lund University, with 13 years of postdoctoral
experience, including three years of international experience .
I’ve got extensive experience in conducting biomedical research, mainly in microbiology/infection
biology but also in tumor biology. I have thus a very broad experience of various lines of research and
am technically quite versatile.
As a person I’m curious, creative and innovative. I’m also persistent and have been productive in
every workplace I’ve been to, something that is reflected in my list of scientific publications in the
appendix of the CV.
I have had both leading and supportive roles in the various projects I have worked on, that is , I can
both be the supportive team player as well as the driving force in a project . I have proved inventive
both in solving smaller technical problems in various projects as well a s making major discoveries. I
have the quality to often see what is missin g in a project and thus to come up with solution to
problem at hand.
PROFESSIONAL EXPERIENCE
Work for Professor Gunnar Lindahl
2012–present
Postdoctoral Researcher
Lund University
Responsibilities
Conducting research on group A streptococci ( Streptococcus pyogenes )
and their interactions with the immune system.
Supervising the younger members of the laboratory .
Writing scientific articles .
Maintaining and genotyping of the transgenic mouse colony as well as
other mouse work.
Responsible for the IT infrastructure of the group (installing computers
and programs).
Achievements
Successfully co-supervised a Ph.D. Student (I was not the official
supervisor) that soon will graduate from the University of Copenhagen.
Successfully co-led a project where we invented and developed a
superior method for the purification of the human blood protein Factor
H. This protein can most likely be used clinically and a patent
application has been filed for the invention. We submitted a patent
application stemming from the conducted research.
As a member of the team I successfully contributed to an important
piece of work where we discovered that many S. pyogenes class I M
proteins bind complement Factor H exclusively to their hypervariable
regions. We also discovered that contrary to general belief, that factor
H did not have any effect on phagocytosis resistance and virulence.
Since S. pyogenes is one of the major human pathogens the M protein
2. CURRICULUM VITAE
Mattias Gustafsson
a very important virulence factor, these findings probably have
importance for understanding streptococcal diseases.
Published a first author article in the prestigious journal PLoS
Pathogens (in vivo article 1 in the appendix).
2010–2012
Successfully maintained a transgenic mouse colony and conducted
research on these.
Submitted a last author manuscript on the Factor H purification method
described above to a scientific journal.
Postdoctoral Researcher
University of Copenhagen
Responsibilities
Conducting research on group A streptococci and their interactions with
the host immune system.
Supervising the younger members of the laboratory.
Writing scientific articles .
Mouse work.
Responsible for the IT infrastructure of the group (installing computers
and programs).
Achievements
2008–2010
I co-supervised a Ph.D. Student (I was not the official super visor). I
helped with ideas for his thesis project. These projects were successful
(see above).
I was involved in an ongoing project were we showed that the S.
pyogenes M protein hypervariable reg ion avoids antibodies both by
antigen variation and poor immunogenicity, something that is very
important for understanding S. pyogenes pathology and vaccine
development. I was drawn into the project when it was already
ongoing. I solved a technical issue regarding the detection of
antibodies which was very important for the rest of the project. This
work was published in the prestigious journal Cell Host & Microbe (in
vivo article 3 in the appendix) where I am shared first author.
Postdoctoral Researcher
Lund University
Responsibilities
Conducting research on group A streptococci and their interactions with
the host immune system.
Supervising the younger members of the laboratory.
Responsible for the IT infrastructure of the group (installing c omputers
and programs).
Achievements
Please see above.
Page 2 of 10
3. CURRICULUM VITAE
Mattias Gustafsson
Work for Professor Catharina Svanborg
2007–2008
Postdoctoral Researcher/Microbiologist
Region Skåne
Responsibilities
Conducting and planning research on the HAMLET (human lactalbuming
made lethal to tumor cells), a protein that kills tumor cells.
Conducting and planning research on urinary tract infections with
Escherichia coli as model bacterium and the interactions with the
immune system.
Supervising the younger members of the laboratory.
Teaching
Achievements
I successfully introduced real time PCR in the laboratory. This led to in
vitro articles 2, 3, 5 and 6 in the appendix. For article 3 I was also the
intellectual sparring partner and suggested biological markers to
measure.
Successfully supervised two exam project students (not the official
supervisor).
Planned and conducted problem based learning (PBL) sessions at the
Biomedicine program at the Medical Faculty at Lund Univers ity.
Tutored at PBL sessions at the courses General Pathology and
Homeostasis at the Medicine program, Medical Faculty, Lund University.
2006–2007
I successfully introduced the use of siRNA technology in the laboratory.
This led to important experiments that led to in vitro articles 2 and 6.
For the project in article 2 I also gave advice in using transgenic cell
lines.
Published research on HAMLET and urinary tract infections in scientific
articles (in vitro articles 2-6and in vivo article 4 in the appendix).
Senior Researcher
HAMLET Pharma
Responsibilities
Conducting and planning research on the HAMLET (human lactalbuming
made lethal to tumor cells), a protein that kills tumor cells.
Conducting and planning research on urinary tract infections with
Escherichia coli as model bacterium and the interactions with the host
immune system.
Supervising the younger members of the laboratory.
Achievements
2004–2006
For scientific achievements, please see above.
Postdoctoral Researcher
Lund University
Responsibilities
Conducting and planning research on urinary tract infections with
Escherichia coli as model bacterium and the interactions with the host
immune system.
Supervising the younger members of the laboratory.
Responsible for the introduction of a range of molecular biology
techniques in Professor Svanborg´s laboratory.
Teaching
Achievements
Successfully introduced a range of molecular biology techniques in
Professor Svanborg´s research group. This fundamentall y changed the
Page 3 of 10
4. CURRICULUM VITAE
Mattias Gustafsson
planning of projects and what was perceived as technically feasible in
the laboratory.
Planned and conducted problem based learning (PBL) sessions at the
Biomedicine program at the Medical Faculty at Lund University.
Produced scientific results that were later published in scientific
journals.
Work for Professor Colin Palmer
2001–2004
Postdoctoral Researcher
University of Dundee
Responsibilities
Conducting research on Peroxisome Proliferator Activated Receptors,
PPARs.
Develop transgenic mice and cell lines for conditional expression of
PPARs.
Maintaining and genotyping of transgenic mice.
Writing scientific articles .
Plan the work and supervise a research assistant.
Achievements
Successfully developed transgenic mice and cell lines for conditional
expression of human PPARδ and a dominant derivative. Interestingly
I discovered that the laboratory had chosen a system for conditional
gene expression in mice that was not going to wor k. Together with
Professor Palmer we chose another system.
I was recruited to a project in the laboratory investigating the role of
PPARδ in the growth of breast and prostate cancer cell lines. I saw that
data on breast cancer cell growth in transgenic cel l lines designed for
conditional expression of PPARδ would be advantageous to the project.
Such data was requested by a reviewer for in vitro article and led to its
acceptance (in vitro article 8 in the appendix).
Successfully led a project in which I supe rvised a research assistant.
This led to a publication (in vitro article 1 in the appendix).
The research for this postdoc period gave rise to five scientific articles
(in vivo articles 2 and 5 and in vitro articles 1, 7 and 8 in the
appendix). Of note, article 8, of which I am the second author, has
been cited over 90 times.
Work for Professor Claes von Wachenfeldt
1995–2000
Ph. D. student
Lund University
Responsibilities
Conducting research on cytochromes P450 in Bacillus subtilis .
Teaching
Responsibility for maintaining some laboratory equipment.
Achievements
For the first part of my Ph.D. studies we collaborated with Professor
Sonenshine´s group in Boston. We discovered a novel mechanism of
resistance to the amino acid antibiotic 4-azaleucine in B. subtilis . We
found that the resistance is due to a mutation in a transcriptional
repressor leading to overproduction of two membrane proteins (then
with unknown function) for branched-chain amino export. I was the
first person in the group that had access to data from a range of
mutant bacteria and I remember the excitement of working out the
mechanism on my own (in vitro article 12 in the appendix) .
Page 4 of 10
5. CURRICULUM VITAE
Mattias Gustafsson
Worked at the University of Dundee with Professor Colin Palmer for a
few months. This work led to in vitro article 11 in the appendix. I was
offered a postdoc position and later went to work for Professor Palmer.
In the work leading to in vitro article 11 was based on discoveries in
the related bacterium Bacillus megaterium , where the gene for a
cytochrome P450 enzyme is preceded by the gene for a transcriptional
repressor. The repressor is displaced from the DNA by certain fatty
acids and the action of the P450 enzyme on the fatty acids ren der
these inactive for binding the repressor. I discovered that the
cytochrome P450 enzyme that we studied might have endogenous
ligands that when metabolized didn’t displace the repressor from the
DNA.
I initiated and led the project where I discovered th at a substance
excreted by wild-type B. subtilis that can overcome the expression of a
range of genes in bacteria mutated in the gene for central
transcriptional regulator Spo0A (in vitro article 10 in the appendix).
Met Professor Andrew Munro at a confer ence and initiated collaboration
with him and Professor Stephen Chapman at the University of
Edinburgh. I suggested that we should study the activity of the
cytochrome P450 enzymes studied on the endogenous branched -chain
fatty acids found in the B. subtilis cell membrane. This led to in vitro
publication 9 in the appendix. I was offered a postdoc position with
Professor Munro.
Supervised a project student
Taught on laboratory practicals on the courses given at the Department
of Microbiology
Thesis with the title ” Bacterial Cytochromes P450: Studies on
cytochrome P450 102A2 and P450 102A3 of Bacillus subtilis .
Published four scientific articles (in vitro articles 9-12 in the appendix).
Of note, article 9 and 12 have been cited over 50 and 60 times,
respectively.
Undergraduate work for Professor Mats Hansson and Professor Lars Hederstedt
1994
Undergraduate student
Lund Univer
Responsibilities
Conducting research on heme biosynthesis in Bacillus subtilis .
Achievements
I constructed the expression systems for production of the heme
biosynthesis enzyme HemY. Only a certain level of production of this
enzyme is tolerated by the bacterium and I was wise enough to salvage
the one or two mutants I got. These were later shown to be promoter
down mutants allowing tolerable overproduction of HemY in B. subtilis .
In the same project I discovered that HemY is strongly associated with
the bacterial membrane, at the time it was thought to only be loosely
associated due to detergent contamination of laboratory equipment .
This work resulted in in vitro article 13 in the appendix.
Page 5 of 10
6. CURRICULUM VITAE
Mattias Gustafsson
EDUCATION
2000
Doctor of Philosophy, Department of Microbiology, Lund
University with Professor Claes von Wachenfeldt as
supervisor.
Key focuses: Molecular biology and biochemistry of cytochromes P450 in
the Gram positive model bacterium Bacillus subtilis .
1995
Bachelor of Science, Lund University , specializing in Microbiology.
Key focuses: In my exam work I studied the biochemistry of the heme
synthesis, see article 1 in the appendix.
Courses: Chemistry, organic chemistry, biochemistry, genetics, molecular
genetics, immunology, physiology, microbiology, geology, ecology,
mathematics etc.
TRAINING
2001
Animal course, University of Aberdeen, U.K. I held a personal license for
working with experimental animals.
2005
University teaching course “Högskolepedagogisk grundkurs” , Medical
Faculty, Lund University.
2005
Problem based learning course, Medical Faculty, Lund University.
2010
Laboratory animal science, Medical Faculty, Lund University .
2011
Researcher’s program, a course in commercializing research, Medeon,
Malmö.
LANGUAGES
Swedish
Native tounge
English
Fluent
PERSONAL DATA
Date of birth:
22 nd of September 1970
Martial status:
Partner Camilla (42)
Children:
Hanna (13)
Interests:
Family life
Nature and the environment. I’m on the board of the local chapter of
Swedish Society for Nature Conservation (Naturskyddsföreningen) . I’m also
a member of “Lunds Botaniska Förening”.
I’m training judo and Brazilian jiu jitsu two to four times a week to keep in
shape.
Page 6 of 10
7. CURRICULUM VITAE
Mattias Gustafsson
APPENDIX
Skills profile
IN VIVO TECHNIQUES
Responsible for breeding transgenic
mice
Marking/biopsy of mice for genotyping
Designed PCR-based genotyping assay
for transgenic mice
Dissecting mice
Isolated RNA from various tissues
Bleeding mice, both by heart
punctuation and by cutting neck
arteries
Intraperitoneal injection of mice
For work regarding molecular biology
techniques regarding mice, please see
above
Assisted in immunization of mice
Assisted in infection of mice
IN VITRO TECHNIQUES
DNA and RNA techniques
PCR
Cloning
Restriction enzyme cleavage analysis
Preparation of chromosomal DNA from
mammalian cells, Bacillus subtilis ,
Streptococcus pyogenes and
Escherichia coli
Preparation of plasmid DNA with
various methods
Transformation of B. subtilis , E. coli
and S. pyogenes
Transfection of mammalian cells
Southern blot
Generation of high frequency of
recombination (Hfr) strains of E. coli
Mapping of genetic markers on the E.
coli chromosome through mating with
a Hfr-strain
Mapping of genetic markers of the B.
subtilis chromosome through threefactor crossings
Mapping of genetic marker on the B.
subtilis chromosome using a YAC
library
Fractionation of restriction enzyme
cleaved chromosomal DNA by
ultracentrifugation
DNA library-construction
DNA library screening
Generation of insertion and insertiondeletion B. subtilis and S. pyogenes as
well as unmarked mutants in B. subtilis
Transposon mutagenesis
Site-directed mutagenesis
Chemical mutagenesis
Generation of random deletions using
exonuclease III and mung bean
nuclease
Sequencing and publishing a DNA
sequence (GenBank accession no.
Y11043)
Generating DNA constructs for non conditional gene-expression in B.
subtilis , E. coli , mammalian cell-lines
and transgenic mice
Generating DNA constructs for
conditional gene-expression in B.
subtilis , E. coli , mammalian cell-lines
and transgenic mice
RNA extraction from B. subtilis , E. coli
and mammalian cells
Generation of cDNA from mammalian
RNA
Northern blot
Real time PCR analysis of mammalian
gene expression using Taqman and
SYBR green chemistry
Protein techniques
T7 protein over-production systems
Disruption of cells using a sonicator
Disruption of cells using a French press
Membrane and cytoplasmic fraction
preparations
Phase fractionation of membrane
proteins using Triton X114
Purification of histidine-tagged
proteins using Ni-agarose columns
Purification of GST-tagged proteins
using glutathione-sepharose columns
Purification of proteins using ion
exchange, gel filtration and ADPsepharose columns
SDS-PAGE
Western blot
Determination of protein
concentrations using various methods
Page 7 of 10
8. CURRICULUM VITAE
Determination of cytochrome P450
concentration by spectrophotometry
Immunocytochemistry
Determination of Kd of Cytochrome
P450s for ligands by
spectrophotometry
Determination Ki of the transcriptional
repressor FatR for various ligands by
EMSA
Mattias Gustafsson
Determination of Kd for FatR using a
direct binding assay with a fluorescent
fatty acid
Investigating enzyme reactions using
spectrophotometric and
spectrofluorometric methods
ELISA
Solid phase RIA
Bacterial ligand and antibody binding
assays
Functional screening assays
Bacterial two-hybrid assays
Investigating PPAR agonist induced
transcriptional transactivation using
mammalian one-hybrid systems
Using mammalian two-hybrid systems
to investigate PPAR/RXR
heterodimerisation and transactivation
Investigating PPAR repression and
agonist induced activation
Bioinformatics
Using the GCG and Staden packages for
handling smaller sequencing projects
Using the GCG package for predicting open
reading frames
Experience with the GCG, MacVector,
Vector NTI and Emboss packages
Using BLAST for finding proteins similar to
unknown open reading frames
Using the GCG package for predicting
transcriptional terminator structures
In silico design of plasmids
Generating phylogenetic trees using the
GCG program package
Predicting transmembrane helices using the
GCG package
Using RasMol for looking at 3D structures of
proteins
Other techniques in microbiology
Gram staining
Typing of bacteria using biochemical and
morphological criteria
Determining generation times of bacteria
One step growth curves of phage T4 of E.
Titration of bacteriophages
Investigating antibiotic resistance of
bacteria
Phase contrast microscopy
coli
Microscopy
General light microscopy
Fluorescence microscopy
TEACHING
Taught in the laboratory practicals of the
following courses given in the biology
program at Lund University (three times for
each course): five and ten credits
Microbiology and ten credits procaryotic
molecular genetics.
Organized a week of the Molecular
Medicine course of the Biomedicine
program at Lund University for two years.
Tutored and wrote problem based
learning cases for one-two weeks on
the Molecular Medicine course of the
Biomedicine program at Lund University
(four times).
Tutored for four weeks on the General
Pathology course of the Medicine program,
Lund University)
Tutored for a half semester on the
Homeostasis course of the Medicine
program, Lund University.
Tutored for two weeks on the Pathobiology
and Pharmacology course on the
Biomedicine program, Lund University.
Page 8 of 10
9. CURRICULUM VITAE
Mattias Gustafsson
MANAGEMENT/SUPERVISION
As a Ph. D. student I supervised a project
student.
As a postdoc in Dundee I led and
planned the work of a research
assistant .
One of my main tasks in Professor
Svanborg´s laboratory was to
supervise members of the laboratory in
molecular biology techniques .
During my appointment as postdoc with
Professor Svanborg’s group I did to some
extent supervise a Ph.D. student (I was not
a formal supervisor). I also supervised two
half semester project students (not a
formal supervisor).
In my current appointment I have to a
large extent supervised a Ph. D. student at
Copenhagen University with Professor
Lindahl and Prof. John Olsen as the formal
supervisors.
IT SYSTEMS
Responsible for installing computers and
programs in our research group.
Been working with Microsoft Windows (XP,
Vista and 7), Mac OS X Mountain Lion.
Microsoft Office (Word, Excel, Power
Point).
Experience with the GCG and Emboss
packages.
Experience with the Staden package.
In silico cloning with MacVector and
VectorNTI
SCIENTIFIC PUBLICATIONS
Articles
In vivo
1.
2.
Gustafsson, M. C., Lannergård, J., Nilsson, O. R., Kristensen, B. M., Olsen, J. E., Harris, C. L.,
Ufret-Vincenty, R. L., Stålhammar-Carlemalm, M., and Lindahl, G. (2013) Factor H binds to
the hypervariable region of many Streptococcus pyogenes M proteins but does not promote
phagocytosis resistance or acute virulence, PLoS Pathog 9, e1003323.
Higgins, L. G., Garbacz, W. G., *Gustafsson, M. C., Nainamalai, S., Ashby, P. R., Wolf, C. R.,
and Palmer, C. N. (2012) Conditional expression of human PPARδ and a dominant negative
variant of hPPARδ in vivo, PPAR research 2012, 216817.
3.
Lannergård, J., Gustafsson, M. C., Waldemarsson, J., Norrby-Teglund, A., StålhammarCarlemalm, M., and Lindahl, G. (2011) The hypervariable region of Streptococcus pyogenes M
protein escapes antibody attack by antigenic variation and weak immunogenicity, Cell Host &
Microbe 10, 147-157.
4.
Ragnarsdóttir, B., Jönsson, K., Urbano, A., Grönbe rg-Hernandez, J., Lutay, N., Tammi, M.,
Gustafsson, M., Lundstedt, A. C., Leijonhufvud, I., Karpman, D., Wullt, B., Truedsson, L.,
Jodal, U., Andersson, B., and Svanborg, C. (2010) Toll -like receptor 4 promoter
polymorphisms: common TLR4 variants may prote ct against severe urinary tract infection,
PLoS One 5, e10734.
5.
Romanowska, M., Reilly, L., Palmer, C. N., Gustafsson, M. C., and Foerster, J. (2010)
Activation of PPARβ/δ causes a psoriasis -like skin disease in vivo, PLoS One 5, e9701.
*Shared first authorship in article 3.
Please note that I didn’t perform any of the human in vivo experiments in article 5.
In vitro/analysis of clinical samples
1.
Nilsson, O. R., Lannergård, J., Morgan, B. P., Lindahl, G. and Gustafsson, M. C. (2013)
Affinity purification of human factor H on polypeptides derived from streptococcal M protein:
enrichment of the Y402 variant, PLoS One , Accepted for publication
2.
Gustafsson, M. C., Knight, D., and Palmer, C. N. (2009) Ligand modulated antagonism of
PPARγ by genomic and non-genomic actions of PPARδ, PLoS One 4, e7046.
3.
Aits, S., Gustafsson, L., Hallgren, O., Brest, P., Gustafsson, M., Trulsson, M., Mossberg, A. K.,
Simon, H. U., Mograbi, B., and Svanborg, C. (2009) HAMLET (human alpha -lactalbumin made
lethal to tumor cells) triggers autophagic tumor cell death, Int J Cancer 124, 1008-1019.
4.
Brest, P., Gustafsson, M., Mossberg, A. K., Gustafsson, L., Düringer, C., Hamiche, A., and
Svanborg, C. (2007) Histone deacetylase inhibitors promote the tumoricidal effect of HAMLET,
Cancer Res 67, 11327-11334.
Page 9 of 10
10. CURRICULUM VITAE
Mattias Gustafsson
5.
Lundstedt, A. C., McCarthy, S., Gustafsson, M. C., Godaly, G., Jodal, U., Karpman, D.,
Leijonhufvud, I., Lindén, C., Martinell, J., Ragnarsdóttir, B., Samuelsson, M., Truedsson, L.,
Andersson, B., and Svanborg, C. (2007) A genetic basis of susceptibility to acute
pyelonephritis, PLoS One 2, e825.
6.
Ragnarsdóttir, B., Samuelsson, M., Gustafsson, M. C., Leijonhufvud, I., Karpman, D., and
Svanborg, C. (2007) Reduced toll-like receptor 4 expression in children with asymptomatic
bacteriuria, J Infect Dis 196, 475-484.
7.
Fischer, H., Ellström, P., Ekström, K., Gustafsson, L., Gustafsson, M., and Svanborg, C.
(2007) Ceramide as a TLR4 agonist; a putative signalling intermediate between sphingolipid
receptors for microbial ligands and TLR4, Cell Microbiol 9, 1239-1251.
8.
Targett-Adams, P., McElwee, M. J., Ehrenborg, E., Gustafsson, M. C., Palmer, C. N., and
McLauchlan, J. (2005) A PPAR response element regulates transcription of the gene for
human adipose differentiation-related protein, Biochim Biophys Acta 1728, 95-104.
9.
Stephen, R. L., Gustafsson, M. C., Jarvis, M., Tatoud, R., Marshall, B. R., Knight, D.,
Ehrenborg, E., Harris, A. L., Wolf, C. R., and Palmer, C. N. (2004) Activation of peroxisome
proliferator-activated receptor δ stimulates the proliferation of human breast and prostate
cancer cell lines, Cancer Res 64, 3162-3170.
10.
Gustafsson, M. C., Roitel, O., Marshall, K. R., Noble, M. A., Chapman, S. K., Pessegueiro, A.,
Fulco, A. J., Cheesman, M. R., von Wachenfeldt, C., and Munro, A. W. (2004) Expression,
purification, and characterization of Bacillus subtilis cytochromes P450 CYP102A2 and
CYP102A3: flavocytochrome homologues of P450 BM3 from Bacillus megaterium , Biochemistry
43, 5474-5487.
11.
Gustafsson, M. C., and von Wachenfeldt, C. (2001) A novel diffusible substance can overcome
the apparent AbrB repression of the Bacillus subtilis fatR promoter, FEMS Microbiol Lett 199,
197-202.
12.
Gustafsson, M. C., Palmer, C. N., Wolf, C. R., and von Wachenfeldt, C. (2001) Fatty -aciddisplaced transcriptional repressor, a conserved regulator of cytochrome P450 102
transcription in Bacillus species, Arch Microbiol 176, 459-464.
13.
Belitsky, B. R., Gustafsson, M. C., Sonenshein, A. L., and von Wachenfeldt, C. (1997) An lrp like gene of Bacillus subtilis involved in branched-chain amino acid transport, J Bacteriol 179,
5448-5457.
14.
Hansson, M., Gustafsson, M. C., Kannangara, C. G., and Hederstedt, L. (1997) Isolated
Bacillus subtilis HemY has coproporphyrinogen III to coproporphyrin III oxidase activity,
Biochim Biophys Acta 1340, 97-104.
Reviews
1.
Ragnarsdóttir, B., Fischer, H., Godaly, G., Grönberg -Hernandez, J., Gustafsson, M., Karpman,
D., Lundstedt, A. C., Lutay, N., Rämisch, S., Svensson, M. L., Wullt, B., Yadav, M., and
Svanborg, C. (2008) TLR- and CXCR1-dependent innate immunity: insights into the genetics
of urinary tract infections, Eur J Clin Invest 38 Suppl 2, 12-20.
2.
Svanborg, C., Bergsten, G., Fischer, H., Godaly, G., Gustafsson, M., Karpman, D., Lundstedt,
A. C., Ragnarsdóttir, B., Svensson, M., and Wullt, B. (2006) Uropathogenic Escherichia coli as
a model of host-parasite interaction, Curr Opin Microbiol 9, 33-39.
3.
Palmer, C. N., Gustafsson, M. C., Dobson, H., von Wachenfeldt, C., and Wolf, C. R. (1999)
Adaptive responses to fatty acids are mediated by the regulated expression of cytochromes
P450, Biochem Soc Trans 27, 374-378.
Ph.D. thesis
1.
Gustafsson, M. C. U. (2000) Bacterial cytochromes P450: Studies on cytochromes P450 102A2
and P450 102A3 of Bacillus subtilis., Department of Microbiology, Lund University, Lund,
Sweden.
Page 10 of 10