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Publications

Publications since 2010


Biferali B, Bianconi V, Perez DF, Kronawitter SP, Marullo F, Maggio R, Santini T, Polverino F, Biagioni S, Summa V, Toniatti C, Pasini D, Stricker S, Di Fabio R, Chiacchiera F, Peruzzi G, Mozzetta C. Prdm16-mediated H3K9 methylation controls fibro-adipogenic progenitors identity during skeletal muscle repair. Sci Adv. 2021; 7(23):eabd9371. DOI: 10.1126/sciadv.abd9371

Comai GE, Tesařová M, Dupé V, Rhinn M, Vallecillo-García P, da Silva F, Feret B, Exelby K, Dollé P, Carlsson L, Pryce B, Spitz F, Stricker S, Zikmund T, Kaiser J, Briscoe J, Schedl A, Ghyselinck NB, Schweitzer R, Tajbakhsh S. Local retinoic acid signaling directs emergence of the extraocular muscle functional unit. PLoS Biol. 2020; Nov 17; 18(11):e3000902. DOI: 10.1371/journal.pbio.3000902

 

Wei X, Franke J, Ost M, Wardelmann K, Börno S, Timmermann B, Meierhofer D, Kleinridders A, Klaus S, Stricker S. Cell autonomous requirement of Neurofibromin (Nf1) for postnatal muscle hypertrophic growth and metabolic homeostasis. Journal of Cachexia, Sarcopenia and Muscle, 2020; 11, 1758-1778 DOI: 10.1002/jcsm.12632

 

Feng C, Chan WCW, Lam Y, Wang X, Chen P, Niu B, Ng VCW, Yeo JC, Stricker S, Cheah KSE, Koch M, Mundlos S, Ng HH, Chan D. Lgr5 and Col22a1 Mark Progenitor Cells in the Lineage toward Juvenile Articular Chondrocytes. Stem Cell Rep. 2019; 13(4), 713-29 DOI: 10.1016/j.stemcr.2019.08.006

 

Stumm J, Vallecilo-Garcia P, vom Hofe-Schneider S, Ollitrault D, Schrewe H, Economides AN, Marazzi G, Sassoon D, Stricker S. Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury. Stem Cell Res. 2018; 32, 8-16 DOI: 10.1016/j.scr.2018.08.010

 

Murgai A, Altmeyer S, Wiegand S, Tylzanowski P, Stricker S. Cooperation of BMP and IHH signaling in interdigital cell fate determination. PLoS ONE 2018; 13(5), e0197535. DOI: 10.1371/journal.pone.0197535

 

Orgeur M, Martens M, Leonte G, Nassari S, Bonnin MA, Börno ST, Timmermann B, Hecht J, Duprez D, Stricker S. Genome-wide strategies identify downstream target genes of connective tissue-associated transcription factors. Development 2018; 145, dev161208 DOI: 10.1242/dev.161208

 

Orgeur M, Martens M, Börno ST, Timmermann B, Duprez D, Stricker S. A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model. Biol. Open 2018; 7, bio028498 DOI: 10.1242/bio.028498

 

Nassari S, Blavet S, Bonnin M-A, Stricker S, Duprez D, Fournier-Thibault C. The chemokines CXCL12 and CXCL14 differentially regulate connective tissue markers during limb development. Sci. Rep. 2017; 7(1), 17279. DOI: 10.1038/s41598-017-17490-z

 

Vallecillo García P, Orgeur M, Vom Hofe-Schneider S, Stumm J, Kappert V, Ibrahim DM, Börno ST, Hayashi S, Relaix F, Hildebrandt K, Sengle G, Koch M, Timmermann B, Marazzi G, Sassoon DA, Duprez D, Stricker S. Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development. Nat. Commun. 2017; 8:1218.DOI: 10.1038/s41467-017-01120-3

 

Dörpholz G, Murgai A, Jatzlau J, Horbelt D, Belverdi MP, Heroven C, Schreiber I, Wendel G, Ruschke K, Stricker S, Knaus P. IRS4, a novel modulator of BMP/Smad and Akt signalling during early muscle differentiation. Sci. Rep. 2017; 7(1), 8778. DOI: 10.1038/s41598-017-08676-6

 

Bernatik O, Radaskiewicz T, Behal M, Dave Z, Witte F, Mahl A, Cernohorsky NH, Krejci P, Stricker S#, Bryja V#. A novel role for the BMP antagonist Noggin in sensitizing cells to non-canonical Wnt-5a/Ror2/Dishevelled pathway activation. Front. Cell Dev. Biol. 2017; 5(47). DOI: 10.3389/fcell.2017.00047

 

Knierim E, Hirata H, Wolf NI, Morales-Gonzalez S, Schottmann G, Tanaka Y, Rudnik-Schöneborn S, Orgeur M, Zerres K, Vogt S, van Riesen A, Gill E, Seifert F, Zwirner A, Kirschner J, Goebel HH, Hübner C, Stricker S, Meierhofer D, Stenzel W, Schuelke M. Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. Am. J. Hum. Genet. 2016; 98(3), 473-89. DOI: 10.1016/j.ajhg.2016.01.006

 

Bourgeois A, Esteves de Lima J, Charvet B, Kawakami K, Stricker S, Duprez D. Stable and bicistronic expression of two genes in somite- and lateral plate-derived tissues to study chick limb development. BMC Dev. Biol. 2015; 15:39. DOI: 10.1186/s12861-015-0088-3

 

Berkholz J, Orgeur M, Stricker S, Munz B. skNAC-and Smyd1 in transcriptional control. Exp. Cell Res. 2015; 336(2), 182-191. DOI: 10.1016/j.yexcr.2015.06.019

 

Maass PG, Aydin A, Luft FC, Schächterle C,Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein I, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, OttJ,Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S. PDE3A mutations cause autosomal-dominant hypertension with brachydactyly. Nat. Genet. 2015; 47(6), 647-653. DOI: 10.1038/ng.3302

 

Pfirrmann T, Emmerich D, Ruokonen P, Auw-Hädrich C, Buchen R, Reinhard T, Fischer-Zirnsak B, Mundlos S, Klopocki E, Stricker S, Hecht J, Krawitz P, Hollemann T, Warman M, Spiekerkötter U, Lausch E, Zabel B, Hoffmann K, Villavicencio-Lorini P. Molecular Pathomechanism of X-linked Megalocornea: Novel Frameshift Mutation in the Stem Cell Niche Factor CHRDL1. Hum. Mol. Genet. 2015; 24(11), 3119-3132. DOI: 10.1093/hmg/ddv063

 

Yiang T, Bassuk AG, Stricker S, Fritzsche B. Prickle1 is necessary for the caudal migration of murine facial branchiomotor neurons. Cell Tiss. Res. 2014; 357(3), 349-361. DOI: 10.1007/s00441-014-1925-6

 

Kuss P, Kraft K, Stumm J, Ibrahim D, Vallecillo-Garcia P, Mundlos S, Stricker S. Regulation of Cell Polarity in the Cartilage Growth Plate and Perichondrium of Metacarpal Elements by HOXD13 and WNT5A. Dev. Biol. 2014; 385(1), 83-93. DOI: 10.1016/j.ydbio.2013.10.013

 

Sartori R, Schirwis E, Blaauw B, Bortolanza S, Zhao J, Enzo E, Stantzou A, Mouisel E, Toniolo L, Ferry A, Stricker S, Goldberg AL, Dupont S, Piccolo S, Amthor H, Sandri M. BMP signaling controls muscle mass. Nat. Genet. 2013; 45(11), 1309-1318. DOI: 10.1038/ng.2772

 

Jamsheer A, Zemojtel T, Kolanczyk M, Stricker S, Hecht J, Krawitz P, Doelken SC, Glazar R, Socha M, Mundlos S. Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. J. Med. Genet. 2013; 50(9), 573-584

 

Maas P, Rump A, Schulz H, Stricker S, Schulze L, Platzer K, Aydin A, Tinschert S, Brennan M, Luft FC, Bähring S. PTHLH and SOX9 dysregulation by a misplaced lncRNA causes brachydactyly. J. Clin. Invest. 2012; 122(11), 3990-4002

 

Ott CE, Hein H, Lohan S, Hoogeboom J, Foulds N, Grünhagen J, Stricker S, Villavicencio-Lorini P, Klopocki E, Mundlos S. Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia. J. Med. Genet. 2012; 49(7), 437-441

 

Klopocki E. Lohan S. Doelken SC. Stricker S. Ockeloen CW. Soares Thiele de Aguiar R. Lezirovitz K. Mingroni Netto RC. Jamsheer A. Shah H. Kurth I. Habenicht R. Warman M. Devriendt K. Kordaß U. Hempel M. Rajab A. Mäkitie O. Naveed M. Radhakrishna U. Antonarakis SE. Horn D. Mundlos S. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. J. Med. Genet. 2012; 49(2), 119-125

 

Stricker S, Mathia S, Haupt J, Seemann P, Meier J, Mundlos S. Odd-skipped related genes regulate differentiation of embryonic limb mesenchyme and bone marrow mesenchymal stromal cells. Stem Cells Dev. 2012; 21(4), 623-633. DOI: 10.1089/scd.2011.0154

 

Baasanjav S, Al-Gazali L, Hashiguchi T, Mizumoto S, Fischer B, Horn D, Seelow D, Ali BR, Aziz SAA, Langer R, Saleh AAH, Becker C, Nürnberg G, Cantagrel V, Gleeson JG, Gomez D, Michel JB, Stricker S, Lindner TH, Nürnberg P, Sugahara K, Mundlos S, Hoffmann K. Faulty initiation of proteoglycan synthesis causes cardiac and joint defects. Am. J. Hum. Genet. 2011; 89(1), 15-27

 

Kossler N*, Stricker S*, Rödelsperger C, Robinson PN Kim J, Dietrich C, Osswald M, Kühnisch J, Stevenson DA, Braun T, Mundlos S, Kolanczyk M. Neurofibromin (Nf1) is required for skeletal muscle development. Hum. Mol. Genet. 2011; 20(14), 2697-2709. DOI: 10.1093/hmg/ddr149

*co-first authors

 

Klopocki E, Lohan S, Brancati F, Koll R, Brehm A, Seemann P, Dathe K, Stricker S, Hecht J, Bosse K, Betz RC, Garaci FG, Dallapiccola B, Jain M, Muenke M, Ng VCW, Chan W, Chan D, Mundlos S. Copy Number Variations (CNVs) involving the IHH locus are Associated with Syndactyly and Craniosynostosis. Am. J. Hum. Genet. 2011; 88(1), 70-75

 

Brancati F, Fortugno P, Bottillo I, Lopez M, Josselin E, Boudghene-Stambouli O, Agolini E, Bernardini L, Bellacchio E, Iannicelli M, Rossi A, Dib-Lachachi A, Stuppia L, Palka G, Mundlos S, Stricker S, Kornak U, Zambruno G, Dallapiccola B. Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. Am. J. Hum. Genet. 2010; 87(2), 265-273

 

Witte F, Chan D, Economides AN, Mundlos S, Stricker S. Receptor tyrosine kinase-like orphan receptor 2 (ROR2) and Indian hedgehog regulate digit outgrowth mediated by the phalanx-forming region. Proc. Natl. Acad. Sci. U.S.A. 2010; 107(32), 14211-14216 DOI: 10.1073/pnas.1009314107

 

Clayton P, Fischer B, Mann A, Mansour S, Rossier E, Veen M, Lang C, Baasanjav S, Kieslich M, Brossuleit K, Gravemann S, Schnipper N, Karbasyian M, Demuth I, Zwerger M, Vaya A, Utermann G, Mundlos S, Stricker S, Sperling K, Hoffmann K. Mutations causing greenberg dysplasia but not pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein. Nucleus2010; 1(4), 1-13

 

Witte F, Bernatik O, Kirchner K, Masek J, Mahl A, Krejci P, Mundlos S, Schambony A, Bryja V, Stricker S. Negative regulation of Wnt signaling by CK1-phosphorylated Dishevelled via Ror2. FASEB J. 2010; 24, 2417-2426 DOI: 10.1096/fj.09-150615

 

Jensen LR, Bartenschlager H, Rujirabanjerd S, Tzschach A, Numann A, Janecke AR, Sporle R, Stricker S, Raynaud M, Nelson J, Hackett A, Fryns JP, Chelly J, de Brouwer APM, Hamel B, Gecz J, Ropers HH, Kuss AW. A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. PathoGenetics 2010; (3)2

 

Liška F, Šnajdr P, Stricker S, Gosele C, Křenová D, Mundlos S, Hübner N. Impairment of Sox9 expression in limb buds of rats homozygous for hypodactyly mutation. Folia Biol. 2010; 56, 58-65

 

Maass PG, Wirth J, Aydin A, Rump A, Stricker S, Tinschert S, Otero M, Tsuchimochi K, Goldring MB, Luft FC, Bähring S. A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E. Hum Mol Genet. 2010; 19(5), 848-860

 

 

 

 

Reviews and Book chapters

 

Helmbacher F, Stricker S. Tissue cross talks governing limb muscle development and regeneration. Sem. Cell Dev. Biol. 2020; 4, 14-30 DOI: 10.1016/j.semcdb.2020.05.005

 

Stricker S, Rauschenberger V, Schambony A. ROR Family Receptor Tyrosine Kinases. In: Andreas Jenny, editor: Curr. Top. Dev. Biol. Vol. 123 (Protein Kinases in Development and Disease), Burlington: Academic Press, 2017; 105-142 DOI: 10.1016/bs.ctdb.2016.09.003

 

Stricker S, Knaus P, Simon HG. Putting Cells into Context. Front. Cell. Dev. Biol. 2017; 5(32), DOI: 10.3389/fcell.2017.00032

 

Spielmann M and Stricker S. Limb Development. In: Inborn Errors of Development (Ed. R.P. Erickson, A. Wynshaw-Boris), Third Edition, Oxford University Press 2016; pp147-160

 

Stricker S and Mundlos S. Development of the Limbs. In: Limb Malformations (S. Mundlos, D. Horn), Springer Verlag Berlin Heidelberg, 2014; pp2-9

 

Stricker S, Mundlos S. FGF and ROR2 receptor tyrosine kinase signaling in human skeletal development. In: Carmen Birchmeier, editor: Curr. Top. Dev. Biol. Vol. 97 (Growth Factors in Development), Burlington: Academic Press, 2011; pp179-206

 

Stricker S, Mundlos S. Mechanisms of digit formation: human malformation syndromes tell the story. Dev. Dyn. (Special issue “limb development” Ed. J. F. Fallon) 2011; 240(5), 990-1004