Les membres de la société recevront les informations de connexion quelques jours auparavant.
Création un réseau international de jeunes chercheurs dans le domaine de la matrice extracellulaire appelé #THEmeshwork. Notre but est de favoriser l’interaction entre les jeunes chercheurs / étudiants / jeunes PIs et de les aider dans le développement de leur carrière.
Vous trouverez plus de détails concernant notre projet dans le flyer ci-dessous.
Julie Di Martino
Ines Velazquez Quesada
Le Laboratoire de Biologie Tissulaire et Ingénierie thérapeutique (LBTI, UMR 5305 CNRS et Université Lyon 1; https://lbti.ibcp.fr/) recherche des candidats en vue de la création d’un poste de Professeur des Universités en Biologie Cellulaire à l’Université Claude Bernard Lyon 1 (section CNU 65). Le (la) candidat(e) devra avoir une solide expertise en Biologie Cellulaire, d’une manière générale, pour les enseignements en Licence, et particulièrement en Biologie Tissulaire, Interactions cellules-matrice extracellulaire, voire Mécanotransduction, pour des enseignements en Master. Le (la) candidat(e) renforcera l’axe « Réparation Tissulaire » de l’Unité et développera un projet en accord avec les thématiques développées par l’Unité, qui consiste à (1) comprendre les mécanismes fondamentaux de l’organisation d’un tissu, (2) comprendre et évaluer la capacité de réponse des tissus à différents types d’agressions extrinsèques et/ou intrinsèques et (3) proposer et tester des approches thérapeutiques innovantes dans le cadre de l’ingénierie tissulaire et de la médecine régénérative. Ainsi, une solide expertise dans l’étude des dialogues dynamiques cellule-cellule ou cellules-microenvironnements au cours des processus d’homéostasie et de réparation tissulaires est demandée.
The Tissue Biology and Therapeutic Engineering Laboratory (LBTI, UMR 5305 CNRS and Université Lyon 1; https://lbti.ibcp.fr/ ) is looking for candidates for a Full Professor position in Cell Biology at the University of Lyon (CNU section 65). The candidate should have a strong expertise (1) in general Cell Biology, for the teaching in Bachelor’s degree, and (2) in Tissue Biology, Cell-extracellular Matrix Interactions and/or in Mechanotransduction, to give lectures in the Master program. The candidate will strengthen the “Tissue repair” axis of the LBTI Unit research and will develop a research project in accordance with the topics that are developed in the research unit :(1) understanding the fundamental mechanisms of tissue organization, (2) understanding and assessing tissue response(s) to different extrinsic and intrinsic insults, and (3) proposing and testing innovative therapeutic approaches in the context of tissue engineering and regenerative medicine. A strong expertise in the study of dynamic cell-cell or cell-microenvironment cross-talks during homeostatis or tissue repair processes is required.
A 3-years PhD student position is available in the group of Patricia Rousselle in the Tissue Biology and Therapeutic Engineering Unit at the Institut de Biologie et Chimie des Protéines (IBCP), Lyon. The topics of research developed will focus on: i) Analysis of the biological properties of a 3D-skin equivalent model, ii) mechanisms involved in skin repair upon treatment with matrix biomimetic- scaffolds in animal models. The LBTI (www.lbti.fr) is well equipped for cell biology, molecular biology and biochemistry and belongs to a larger campus (SFR BioSciences Gerland – Lyon Sud (US8 / UMS3444, https://www.sfr- biosciences.fr/), giving access to state-of-the-art core facilities in areas ranging from animal models to protein science such as animal facilities, bioimaging, biomolecular analysis, proteomics, structural biology and production and analysis of proteins. Working languages of the laboratory are English and French.
We are looking for enthusiastic, self-motivated individuals with a background in tissue and cell biology and Imaging techniques. Know-how in cell culture and microscopic techniques is recommended. Excellent adaptability to team-work in different environments and mobility is absolutely required.
Starting date: January, 2021 or earlier (to be discussed).
Please send your CV, names of referees and a short informal description of yourself as a single PDF file to: firstname.lastname@example.org
Dead line for applications: September 7, 2020.
ISMB announces the Opening of the Call for Nominations for the 2020 Distinguisher Investigator Award.
This Award is given by the International Society for Matrix Biology to an established researcher in recognition of important lifetime achievements in the field of Matrix Biology.
A list of the former winners is given at https://ismb.org/prizes/
The Awardee will give the ISMB Distinguished Investigator Lecture at the 2020 ASMB Biennial Conference, Nov. 8-11th 2020 in St. Louis, Missouri.
ISMB members are invited to send in their nominations for the Distinguished Investigator Awardee 2020. Please provide:
- A full curriculum vitae of the nominee, including a list of their publications.
- A letter of nomination that highlights key lifetime research achievements in the field of Matrix Biology.
These nominations will be voted on by the ISMB Council.
Please send nomination packs to the ISMB Secretary (email@example.com) by 31stJan. 2020 at the latest.
Call for Nominations for New ISMB Council Members.
There are two vacancies to serve on the ISMB Council and we are calling for nominations or volunteers to fill these. If you wish to nominate someone, please make sure first that they agree to be nominated.
The vacancies are for:
1 regular ISMB Council member (from any region of the world) and
1 early-career Council member (from any region of the world).
The main responsibilities of regular Council members are to promote the Aims of ISMB in the international matrix biology community in general, and to take part in ISMB Council meetings by teleconference or in-person at conferences, to vote in the Awards processes, and to take part in nominations for Executive officers of Council. The ISMB statutes are available at https://ismb.org/bylaws/
The early-career Council member will have involvement in the Communications sub-group and social media activities and in raising awareness of ISMB amongst early career researchers, and will take part in ISMB Council meetings by teleconference or in-person at conferences.
All Council members serve a 3 year term in the first instance, with the option of renewal for a further 3 years.
Please send names, contact details and biosketch of Council nominees to the ISMB Secretary, firstname.lastname@example.org by 27th January 2020.
Laboratoire LYOS INSERM UMR 1033 – Equipe 2 Bone, Cancers and Metastases – Université de Lyon
Rôle des Lysyl Oxydases dans la progression tumorale
Le Docteur Caroline REYNAUD a soutenu son Habilitation à Diriger des Recherches le 19 novembre 2019 devant un jury composé de :
- Pr Ulrich VALCOURT, président
- Dr Catherine MONNOT, rapporteur
- Pr Maxime LEHMANN, rapporteur
- Pr Laurent DUCA, rapporteur
- Dr Philippe CLEZARDIN, examinateur
ISMB IS PLEASED TO ANNOUNCE THE OPENING OF THE COMPETITION TO IDENTIFY THE 2020 RUPERT TIMPL AWARD WINNER.
The International Society for Matrix Biology created in 2004 a prize dedicated to the memory of the outstanding matrix biologist, Rupert Timpl, who died on October 20th, 2003. The prize is called the « Rupert Timpl Award ».
The prize is awarded biannually at the occasion of the Matrix Biology Europe /FECTS meeting. It is given to a young matrix biologist at an early stage of their scientific career, in general below 40 years of age, who has published the « BEST PAPER IN THE FIELD OF MATRIX BIOLOGY » during the two years prior to the year of the MBE/FECTS meeting.
As an integral part of the programme, the laureate will give a plenary lecture, called the Rupert Timpl Lecture, at the 2020 MBE meeting to be held in Florence, Italy, 24-28 May, 2020.
A prize of EUR 2,000 will be given, which is generously sponsored by Elsevier, the publisher of Matrix Biology.
ISMB MEMBERS ARE INVITED TO SEND THEIR NOMINATIONS FOR THE AWARDEE TO THE ISMB SECRETARY (JO.ADAMS@BRISTOL.AC.UK) BY 31ST DEC. 2019.
The nominations will be voted on by ISMB Council and the winner will be
announced in January 2020.
Eligibility: The nominee should be a young matrix biologist at an early stage of their scientific career, in general below 40 years of age, who has published the « BEST PAPER IN THE FIELD OF MATRIX BIOLOGY » during 2018 and 2019.
Please provide for your nomination:
A letter of support that includes a rationale for the nomination and the
specific paper published in 2018 or 2019 for consideration.
The nominee’s CV, with inclusion of a full list of publications.
With best wishes,
The Laboratory of Tumor and Developmental Biology, GIGA-Cancer, at the University of Liège (Belgium) has an opening for a PhD candidate on breast cancer resistance to targeted therapies (PI: Nor Eddine SOUNNI, team cancer and metabolism)
Topic: Targeting breast cancer metastasis
Despite advances in targeted therapies against HER2+, the presence of intrinsic and/or acquired resistance to anti-HER2 therapy remains an important challenge in breast cancer. In the triple negative breast cancer (TNBC), while it expresses high level of EGFR, anti-EGFR targeted therapies in combination with chemotherapies were generally unsatisfactory in clinical trials. This project is based on our recent paper (Foidart et al. 2019, Clinical Cancer Research) in which we demonstrated the clinical relevance of 3 molecules, EGFR, MT4-MMP and RB in TNBC and showed efficacy of targeting EGFR and CDK4/6 in 50% of TNBC expressing MT4-MMP, EGFR and RB. The new project aim is to understand mechanism(s) of MT4-MMP in breast cancer progression. We will investigate the repertoire of substrates of MT4-MMP by iTRAQ and MS analysis. We will validate the role of the target substrate and perform functional assays for evaluating their role in breast cancer proliferation and migration in vitro, and tumor growth and metastasis in vivo. Our ultimate goal is to propose new therapies for the untreatable TNBC and for therapy resistant HER2+ breast cancer.
Technically, the project involves cell culture, siRNAs, proliferation and migration assays, western blots and immunoprecipitations, and in vivo study using xenografts and PDX for tumor growth and metastasis.
The ideal candidate will be highly motivated and have a Master in Biomedical Sciences/Biology/Biochemistry.
The available funding is 4 years Télévie grant (F.R.S-FNRS) starting on October 1st 2019.
Interested candidates should send their résumé and application letter to Dr. Nor Eddine SOUNNI (email@example.com).
We are looking for a highly motivated PhD student interested in immunology and the extracellular matrix to join our dynamic and international team at the Department of Dermatology, Medical Center – University of Freiburg, Germany. The project will focus on delineating the role of the lymphoid extracellular matrix in maintenance of systemic and skin immune homeostasis. Genetic skin blistering diseases will be used as models. For the studies, analyses of patient-derived samples, ex vivo and in vivo models will be employed. Practical knowledge of cell culture, basic immunological and biochemical analyses is needed; FELASA B certification or equivalent is an advantage. The position is fully funded for four years and part of a collaborative research center on immunology.
To apply, please send motivation letter with CV and contact information of three references to PD. Dr. Dimitra Kiritsi and Dr. Alexander Nyström
We are looking forward to your application!
Application deadline: August 1st.
Starting date: September 1st
Funded by: DFG, German Research Foundation
Duration: 4 years
Contact: Dr. Alexander Nyström firstname.lastname@example.org PD. Dr. Dimitra Kiritsi email@example.com
Nyström A et al.,. 2018. Impaired lymphoid extracellular matrix impedes antibacterial immunity in epidermolysis bullosa..Proc Natl Acad Sci U S A.
Kühl T et al.,. 2016. Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of Genodermatoses. J Invest Dermatol.
Föll MC et al., 2018. Identification of tissue damage, extracellular matrix remodeling and bacterial challenge as common mechanisms associated with high-risk cutaneous squamous cell carcinomas..Matrix Biol
Spörrer M et al.,. 2019. Treatment of keratinocytes with 4-phenylbutyrate in epidermolysis bullosa: Lessons for therapies in keratin disorders. EBioMedicine.
CELL-MATRIX SIGNALLING IN SKIN REPAIR
PROTEASES AS MEDIATORS OF TISSUE REPAIR
The closing date is the 7th June.
DR MICHAEL J SHERRATT
Senior Lecturer in Molecular Biochemistry
Associate Lead for PEP Years 1 and 2
Division of Cell Matrix Biology and Regenerative Medicine
School of Biological Sciences
Faculty of Biology Medicine and Health
The University of Manchester I Room 1.529, Stopford Building
Manchester M13 9PT
Tel (+44) 161 275 1439
Rôle des ostéocytes dans la régénération osseuse assistée par les biomatériaux.
A two-year postdoctoral position is opening at the Institute of Materials (iMat) of the University Paris-Seine (Cergy-Pontoise). The project includes two labs of iMat: LPPI (Polymer chemistry) and ERRMECe (Biology)
In vivo, cells are surrounded by the extracellular matrix (ECM), a 3D-meshwork of macromolecules. A great variety of dynamic biochemical, biophysical, topographical and electrical clues emanates from ECM. They govern cell survival, differentiation and others behaviors, and subsequently physiopathological processes. Especially, the microenvironment modulates cell phenotype and could subsequently orient cells’ response to drug agents and targeted therapies. To take into account this native 3D-environment in cell-based assays, various supports have been developed. They are classified as scaffold-free (like spheroids) or scaffold-based supports (hydrogels, porous/fibrous scaffold) and are made respectively from natural ECM-derived molecules or synthetic material. Among common synthetic commercial scaffolds, there are microfabricated scaffolds and the widely described electrospun fiber mats. Poly(High Internal Phase Emulsion) (polyHIPEs) presenting interconnected porous structures, have been described also as really promising 3D templates [3,4] but are, up to now, only available at laboratory scale.
Despite their advantages in terms of robustness, reproducibility and tunability in comparison to natural ECM-derived materials, these synthetic scaffolds rarely incorporate ECM molecules, thus losing the “biochemical component” of cell microenvironment. Moreover, such scaffolds display limited and uncontrolled dynamic and often lack the combined regulatory inputs as porosity, elasticity, topography, or electrical clues from the ECM that all contribute to modulating cell survival and functions. In this context, the emergence of electroactive materials is of critical interest to mimic the environment of demanding cells regarding mechanical, morphological or electrical stimulation. Such materials represent a fast growing field and rely on the coatings of 3D porous structures with conducting materials. For instance, graphene coating on silk fibroin fiber mats, providing electrical conduction, improved the differentiation of PC-12 cells into neural phenotypes. Coating with a conducting polymer (polyaniline) on similar scaffolds allowed electrical stimulation and enhanced differentiation of myogenic (muscle) C2C12 cells. In addition to simple electrical conduction, conducting polymers (CPs), as electroactive polymers, can also provide additional functions rarely described in this field. Indeed, they are also able to change shape/volume and/or mechanical properties when electrochemically oxidized or reduced. Actually, when CPs are stimulated using low potentials (~ 1V), exchanges (insertion/expulsion) of counter-ions with surrounding electrolyte takes place, leading to electrochemically controllable volume changes thus, allowing both electrical and mechanical stimulations.
LPPI has described the first rubbery electroactive electrospun scaffolds based on elastomer (Nitrile Butadiene Rubber) and polyethylene oxide (PEO) functionalized by a conducting polymer (poly(3,4- ethylenedioxythiophene) (PEDOT)[9,10]. Not evaluated yet as electroactive cell culture scaffolds, they presented promising actuation and beating functionalities in the presence of phosphate buffered saline (PBS). Preliminary data suggest their cytocompatibility. More recently conducting polymer coating has been used by Jager et al. to provide mechanical beating functionality to poly(lactic-co- glycolic acid) (PLGA) electrospun fibers and resulted in increased expression of cardiac markers of stem cells. Nevertheless this unique example of mechanically active culture scaffolds displayed limited volume variations due to the high stiffness of PLGA fibers, highlighting the need of soft and rubbery 3D templates for efficient electroactive behavior. It is worth mentioning that polyHIPEs have never been functionalized by any electroactive material contrary to electrospun fiber mats.
In the frame of 3DEStim, we propose:
- To develop 3D electroactive scaffolds for cell culture combining both electrical and mechanical stimulation. Such materials will be elaborated first from highly porous polyHIPE structures. A conducting polymer will be embedded into this matrix by oxidative chemical vapor phase polymerization of corresponding monomer.
- To functionalize these scaffolds with adhesive ECM glycoproteins for displaying controlled properties and signal dynamic of in vivo cell environments. The cells responses to such ECM- containing scaffolds will be then studied.
- To establish the proof of the concept of using such a device for drug response screening, firstly focusing on anticancer drug response, especially of ovarian cancer metastasis by tuning the scaffold to model their peritoneum implantation site, which displays in vivo dynamic resulting from breathing, digestion, and bodily movements.
Thereafter, capitalizing on the acquired know-how, the 3D electoactive scaffold features as well as its ECM functionalization will be adapted to varied cell types in regard with the desired drug assays
- PhD in Polymer Chemistry or biomaterials
- Relevant research experience and demonstrated competencies in polymer and material
synthesis. Experience in biomaterials and cell culture would be an asset
- Track record of researcher dissemination including peer-reviewed publications
- Ready to work according to best chemical or biology laboratory practices including lab safety.
- Excellent project management, analytical, and report writing skills.
- Excellent communication skills (oral, written, presentation).
- Demonstrated ability to generate new ideas, concepts, models and solutions.
- Collaborative skills, initiative, result oriented, organization, and capacity to work in an
- French and/or English
- less than 6 months in France since the last 3 years.
 Knight at al. J Anat. (2015), 227(6): 746–756.
 Moglia R.S. et al. Biomacromolecules (2014), 15, 2870−2878.
 McGann C.L. et al. Polymer (2017), 126, 408-418
 Kofron et al. J Physiol (2017), 595(12), 3891-3905.
 Aznar-Cervantes et al. Materials Science and Engineering: C (2017), 79, 315-325
 Zhang et al. Macromolecular Bioscience (2017) 17(9), 1700147
 Otero et al. J. Mater. Chem. B, 2016, 4, 2069–2085
 Kerr-Phillips et al. J. Mater. Chem. B, 2015,3, 4249-4258
 Kerr-Phillips et al. Biosensors and Bioelectronics, 2018, 100, 549-555, ISSN 0956-5663
 Gelmi et al. Adv. Healthcare Mater.2016, 5, 1471–1480
Le sujet porte sur la « MISE EN PLACE D’UN MODÈLE BIOLOGIQUE DE CARACTÉRISATION _IN VITRO_ DES PROPRIÉTÉS ANGIOCONDUCTRICES ET ANGIOGÉNIQUES DE CÉRAMIQUES PHOSPHOCALCIQUES ». L’étudiant.e sera inscrit.e à l’École Doctorale n°609 Sciences et Ingénierie des Matériaux, Mécanique, Énergétique – SIMME de l’Université de Limoges.
Cette thèse sera effectuée au sein de l’équipe « Biocéramiques » de l’IRCER (Institut de Recherche sur les Céramiques ), UMR CNRS 7315 à l’Université de Limoges.
L’étudiant.e recherché.e sera titulaire d’un Master 2 Recherche, préférentiellement dans le domaine des Sciences de la Vie et plus particulièrement avec une spécialisation en biologie cellulaire et moléculaire. Il.Elle devra être sensibilisé.e au domaine des biomatériaux et devra être à même de travailler en équipe pluridisciplinaire.
Le candidat doit être autonome et doit avoir acquis une expérience en biologie cellulaire et moléculaire. Une bonne maîtrise des techniques de culture cellulaire et d’analyse du phénotype et des fonctions cellulaires est souhaitée.
Contacts (renseignements et candidature) : Amandine Magnaudeix et Eric
Champion (firstname.lastname@example.org ; email@example.com )
Keywords: biomimicry, protein self-assembly, adhesion, surfaces.
- Context and mission
In our daily lives, all conventional man-made adhesives are petrochemical products, which are toxic for the body and show limited efficiency in wet conditions, major drawbacks for biomaterials. In this project, we aim at producing adhesives effective in air and/or in wet conditions inspired by natural glues of some arthropods. This approach using simplified mimics of biological adhesives will facilitate better understanding of systems from which they are derived and could find applications in medicine as well as in biotechnology and industry.
Adhesive proteins of some arthropods have been identified. For these animals, the adhesion mechanism seems to be related to protein self-assembly on the surface. The molecular basis of this process has been elucidated by our team but its mechanisms remain to be elucidated. The goal of the PhD project is to produce adhesive proteins mimicking the natural one, to investigate the self-assembly process of these proteins and their adsorption/adhesion on materials. To achieve this goal, the project will involve a genetic engineering strategy, protein characterization approaches using biophysics and microscopies.
- Candidate profile
We look for a highly motivated candidate with a strong knowledge in biochemistry, biophysics and/or in material science. The student should be able to work in a team, have very good writing skills (report, presentation…) and good knowledge of at least one of the language used in the lab: French, English.
- The Laboratory and the team
The project will take place within “Equipe de Recherche sur les Relations Matrice Extracellulaire- Cellules” (ERRMECE: EA1391) from Cergy-Pontoise University (http://www.u-cergy.fr/errmece/), in collaboration with the “Laboratoire des Matériaux et du Génie Physique”(LMGP: UMR 5628) in the Grenoble Institute of Technology (http://www.lmgp.grenoble-inp.fr/), known worldwide for its expertise in material science.
The ERRMECE lab is composed of 18 staff members and is organized in three research groups:
– BioSan: this team works on biomatrerials, especially on layer by layer films and interpenetrated network technologies;
– BCMI: this team works on microbial biofilms and anti-fouling strategies;
– MecUp: this team works on human extracellular matrix in physico-pathological contexts. Hence the lab has extensive expertise in the study of different extracellular matrices, on their composition and function, in relationships with cells and the functionalization of materials. The PhD project proposes new “matrix-like” models for the ERRMECe lab and will reinforce the axis on protein- material interactions by the collaboration with the LMGP.
Charlotte Vendrely, Uni. de Cergy-Pontoise, ERRMECe ; firstname.lastname@example.org
The position is available for 3 years starting from: October 1, 2019.
Application dead-line is: May 17, 2019.
Equipe de Recherche sur les Relations Matrice Extracellulaire-Cellules-ERRMECe
Maison Internationale de la Recherche Rue Descartes
95031 Neuville sur Oise Cedex France
La SFD a créé trois bourses de 1.500,00 euros pour financer la participation de jeunes dermatologues ou chercheurs au congrès de l’European Society for Dermatological Research.
Le prochain congrès « ESDR 2019 » aura lieu du 18 au 21 septembre 2019, à Bordeaux.
Vous trouverez ici un dossier de candidature pour cette bourse. Elle est réservée à un(e) jeune dermatologue, CCA ou interne ayant une communication orale ou affichée acceptée au congrès 2019, ou à un jeune chercheur médecin ou scientifique, participant, ou ayant participé à des projets de recherche en dermatologie, de moins de 35 ans, et ayant une bonne connaissance de l’anglais.
Les dossiers sont à renvoyer avant le 30 avril 2019 à Madame Anne-Laure Geoffroy, par mail email@example.com, ou par courrier : Bourses ESDR 2019, Maison de la Dermatologie, 10 Cité Malesherbes, 75009 Paris.
Société Française de Dermatologie
Maison de la Dermatologie
10, Cité Malesherbes
75009 Paris FRANCE
Dulce Papy Garcia (Gly-CRRET, UPEC, Créteil) and Romain Vives (IBS, Grenoble) are glad to invite you to participate to the next INSERM (French national institute for Health Sciences) international workshop on Glycosaminoglycans that will take place in Bordeaux, on the 19-21th of June 2019.
The goal of this workshop is to put an emphasis on the technological developments and breakthroughs that led to progress in the understanding of GAG structure and biological functions, as well as the perspectives of applications in diagnostics and therapy.
The workshop will include 4 main sessions focusing on :
- GAG Biosynthesis and Metabolism
Confirmed speakers : L. Kjellen (Uppsala Univ., Uppsala, Sweden) – L. Pedersen (South Carolina Univ., Chapel Hill, USA) – A. Malmström (Lund Univ., Lund, Sweden) – R. Vivès (IBS, Grenoble, France) – S. Fournel Gigleux (Nancy Univ., Nancy, France)
- GAG-protein interactions and physiophatological conditions
Confirmed speakers : H. Lortat-jacob (IBS, Grenoble, France) – A. Vortkamp (Essen Univ., Essen, Germany) – D. Papy-Garcia (Université Paris Est, Créteil, France) – J. van den Born, (Groningen Univ., Groningen, The Netherlands) – P. Nieto (Spanish National Research Council, Sevilla, Spain)
- Technological and methodological approaches for GAG analysis
Confirmed speakers : T. van Kuppevelt (Radboud Univ, Nijmegen, Pays-bas) – S. Ricard-Blum (Université de Lyon I, Lyon, France) – D. Bonnaffé (ICMMO, Orsay, France) – F. Noborn (Gothenburg Univ., Gothenbur, Sweden)
- GAGs : from bench to bedside
Confirmed speakers : P. Albanese (Université Paris Est, Créteil, France) – Yongmei Xu (South Carolina Univ., Chapel Hill, USA) – F. Chiapini (OTR3, Paris, France)
Registration are open (deadline 15/04) and all details can be found on: Atelier INSERM 256
The special issue given below is online.
Thanks to the contributions by well known authors in the field, another key area of matrix biology has been published.
Many thanks to editor-in-chief Renato Iozzo for giving us the opportunity and his great support during all steps of this endeavor !
I hope it will be a useful for your future research.
All the best