Publikationen
Ausgewählte Publikationen
Liu H, Ding J, Köhnlein K, Urban N, Ori A, Villavicencio-Lorini P, Walentek P, Klotz LO, Hollemann T, Pfirrmann T (2020) The GID ubiquitin ligase complex is a regulator of AMPK activity and organismal lifespan. AUTOPHAGY, 16: 1618-1634
Schulz S, Porsch M, Grosse I, Hoffmann K, Schaller HG, Reichert S (2019) Comparison of the oral microbiome of patients with generalized aggressive periodontitis and periodontitis-free subjects. ARCHIVES OF ORAL BIOLOGY, 99: 169-176
Porsch M, Özdemir E, Wisniewski M, Graf S, Bull F, Hoffmann K, Ignatov A, Haybaeck J, Grosse I, Kalinski T, Nass N (2019) Time resolved gene expression analysis during tamoxifen adaption of MCF-7 cells identifies long non-coding RNAs with prognostic impact. RNA Biology, 16: 661-674
Moosa S, Yamamoto GL, Garbes L, Keupp K, Beleza-Meireles A, Moreno CA, Valadares ER, de Sousa SB, Maia S, Saraiva J, Honjo RS, Kim CA, Cabral de Menezes H, Lausch E, Lorini PV, Lamounier A, Carniero TCB, Giunta C, Rohrbach M, Janner M, Semler O, Beleggia F, Li Y, Yigit G, Reintjes N, Altmüller J, Nürnberg P, Cavalcanti DP, Zabel B, Warman ML, Bertola DR, Wollnik B, Netzer C (2019) Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta. AMERICAN JOURNAL OF HUMAN GENETICS, 105: 836-843
7Marsch WC, Komatsuzaki S, Mueller A, Hagemann M, Lange D, Maemecke L, Villavicencio-Lorini P, Hoffmann K (2019) Livedoid vasculopathy: does hyperhomocysteinaemia play an aetiological role? EUROPEAN JOURNAL OF DERMATOLOGY, 29: 287-293
Kraya T, Quandt D, Pfirrmann T, Kindermann A, Lampe L, Schroeter ML, Kohlhase J, Stoevesandt D, Hoffmann K, Villavicencio-Lorini P (2019) Functional characterization of a novel CSF1R mutation causing hereditary diffuse leukoencephalopathy with spheroids. Molecular Genetics & Genomic Medicine, 7: e00595
Kappler M, Pabst U, Weinholdt C, Taubert H, Rot S, Kaune T, Kotrba J, Porsch M, Güttler A, Bache M, Krohn K, Bull F, Riemann A, Wickenhauser C, Seliger B, Schubert J, Al-Nawas B, Thews O, Grosse I, Vordermark D, Eckert AW (2019) Causes and Consequences of A Glutamine Induced Normoxic HIF1 Activity for the Tumor Metabolism. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 20: epub
Hüneburg R, Aretz S, Büttner R, Daum S, Engel C, Fechner G, Habermann JK, Heling D, Hoffmann K, Holinski-Feder E, Kloor M, von Knebel-Döberitz M, Loeffler M, Möslein G, Perne C, Redler S, Rieß O, Schmiegel W, Seufferlein T, Siebers-Renelt U, Steinke-Lange V, Tecklenburg J, Vangala D, Vilz T, Weitz J, Wiedenmann B, Strassburg CP, Nattermann J (2019) [Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients]. ZEITSCHRIFT FUR GASTROENTEROLOGIE, 57: 1309-1320
Fischer-Zirnsak B, Koenig R, Alisch F, Güneş N, Hausser I, Saha N, Beck-Woedl S, Haack TB, Thiel C, Kamrath C, Tüysüz B, Henning S, Mundlos S, Hoffmann K, Horn D, Kornak U (2019) SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy. JOURNAL OF HUMAN GENETICS, 64: 609-616
Arslan M, Devisetty UK, Porsch M, Große I, Müller JA, Michalski SG (2019) RNA-Seq analysis of soft rush (Juncus effusus): transcriptome sequencing, de novo assembly, annotation, and polymorphism identification. BMC GENOMICS, 20: 489
Schleinitz D, Seidel A, Stassart R, Klammt J, Hirrlinger PG, Winkler U, Köhler S, Heiker JT, Schönauer R, Bialek J, Krohn K, Hoffmann K, Kovacs P, Hirrlinger J (2018) Novel Mutations in the Asparagine Synthetase Gene (ASNS) Associated With Microcephaly. Frontiers in Genetics, 9: 245
Hause F, Schlote D, Simm A, Hoffmann K, Santos AN (2018) Accumulation of glycated proteins suggesting premature ageing in lamin B receptor deficient mice. BIOGERONTOLOGY, 19: 95-100
Bonnin E, Cabochette P, Filosa A, Jühlen R, Komatsuzaki S, Hezwani M, Dickmanns A, Martinelli V, Vermeersch M, Supply L, Martins N, Pirenne L, Ravenscroft G, Lombard M, Port S, Spillner C, Janssens S, Roets E, Van Dorpe J, Lammens M, Kehlenbach RH, Ficner R, Laing NG, Hoffmann K, Vanhollebeke B, Fahrenkrog B (2018) Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence. PLoS Genetics, 14: e1007845
Schnipper N, Stassen HH, Kallinich T, Sperling K, Hoffmann K (2017) Image analysis of neutrophil nuclear morphology: Learning about phenotypic range and its reliable analysis from patients with pelger-Huët-anomaly and treated with colchicine. CYTOMETRY PART B-CLINICAL CYTOMETRY, 92: 541-549
Scheller K, Kalmring F, Scheller C, Schubert J, Bialek J (2017) Oral vitamin B1-substitution does not decrease genetically determined cleft rate in mice (A/WySn). JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY, 45: 1948-1954
Foja S, Luther M, Hoffmann K, Rupprecht A, Gruenauer-Kloevekorn C (2017) CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs' dystrophy. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 255: 1621-1631
Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D (2017) Familial Gordon syndrome associated with a PIEZO2 mutation. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 173: 254-259
Ziesenitz VC, Loukanov T, Gläser C, Gorenflo M (2016) Variable expression of Alagille syndrome in a family with a new JAG1 gene mutation. CARDIOLOGY IN THE YOUNG, 26: 164-7
Willkomm L, Heredia R, Hoffmann K, Wang H, Voit T, Hoffman EP, Cirak S (2016) Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegia. JOURNAL OF HUMAN GENETICS, 61: 571-3
Seemanova E, Varon R, Vejvalka J, Jarolim P, Seeman P, Chrzanowska KH, Digweed M, Resnick I, Kremensky I, Saar K, Hoffmann K, Dutrannoy V, Karbasiyan M, Ghani M, Barić I, Tekin M, Kovacs P, Krawczak M, Reis A, Sperling K, Nothnagel M (2016) The Slavic NBN Founder Mutation: A Role for Reproductive Fitness? PLoS One, 11: e0167984
Schulz S, Lüdike H, Lierath M, Schlitt A, Werdan K, Hofmann B, Gläser C, Schaller HG, Reichert S (2016) C-reactive protein levels and genetic variants of CRP as prognostic markers for combined cardiovascular endpoint (cardiovascular death, death from stroke, myocardial infarction, and stroke/TIA). CYTOKINE, 88: 71-76
Schulz S, Immel UD, Just L, Schaller HG, Gläser C, Reichert S (2016) Epigenetic characteristics in inflammatory candidate genes in aggressive periodontitis. HUMAN IMMUNOLOGY, 77: 71-5
Miehle K, Porrmann J, Mitter D, Stumvoll M, Glaser C, Fasshauer M, Hoffmann K (2016) Novel peroxisome proliferator-activated receptor gamma mutation in a family with familial partial lipodystrophy type 3. CLINICAL ENDOCRINOLOGY, 84: 141-8
Luther M, Grünauer-Kloevekorn C, Weidle E, Passarge E, Rupprecht A, Hoffmann K, Foja S (2016) [TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy]. KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 233: 187-94
Li Y, Salfelder A, Schwab KO, Grünert SC, Velten T, Lütjohann D, Villavicencio-Lorini P, Matysiak-Scholze U, Zabel B, Köttgen A, Lausch E (2016) Against all odds: blended phenotypes of three single-gene defects. EUROPEAN JOURNAL OF HUMAN GENETICS, 24: 1274-9
Kouz K, Lissewski C, Spranger S, Mitter D, Riess A, Lopez-Gonzalez V, Lüttgen S, Aydin H, von Deimling F, Evers C, Hahn A, Hempel M, Issa U, Kahlert AK, Lieb A, Villavicencio-Lorini P, Ballesta-Martinez MJ, Nampoothiri S, Ovens-Raeder A, Puchmajerová A, Satanovskij R, Seidel H, Unkelbach S, Zabel B, Kutsche K, Zenker M (2016) Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation. GENETICS IN MEDICINE, 18: 1226-1234
Job F, Mizumoto S, Smith L, Couser N, Brazil A, Saal H, Patterson M, Gibson MI, Soden S, Miller N, Thiffault I, Saunders C, Yamada S, Hoffmann K, Sugahara K, Farrow E (2016) Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype. BMC Medical Genetics, 17: 86
Foja S, Hoffmann K, Auw-Haedrich C, Reinhard T, Rupprecht A, Gruenauer-Kloevekorn C (2016) Identification of two novel mutations in the cornea-specific TGFBI gene causing unique phenotypes in patients with corneal dystrophies. INTERNATIONAL OPHTHALMOLOGY, 36: 867-873
Wege N, Schutkowski A, Boenn M, Bialek J, Schlitt A, Noack F, Grosse I, Stangl GI (2015) Men and women differ in their diurnal expression of monocyte peroxisome proliferator-activated receptor-α in the fed but not in the fasted state. FASEB JOURNAL, 29: 2905-11
Sauer SW, Opp S, Komatsuzaki S, Blank AE, Mittelbronn M, Burgard P, Koeller DM, Okun JG, Kölker S (2015) Multifactorial modulation of susceptibility to l-lysine in an animal model of glutaric aciduria type I. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1852: 768-77
Pfirrmann T, Villavicencio-Lorini P, Subudhi AK, Menssen R, Wolf DH, Hollemann T (2015) RMND5 from Xenopus laevis is an E3 ubiquitin-ligase and functions in early embryonic forebrain development. PLoS One, 10: e0120342
Pfirrmann T, Emmerich D, Ruokonen P, Quandt D, Buchen R, Fischer-Zirnsak B, Hecht J, Krawitz P, Meyer P, Klopocki E, Stricker S, Lausch E, Seliger B, Hollemann T, Reinhard T, Auw-Haedrich C, Zabel B, Hoffmann K, Villavicencio-Lorini P (2015) Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model. HUMAN MOLECULAR GENETICS, 24: 3119-32
Luetzkendorf J, Nerger K, Hering J, Moegel A, Hoffmann K, Hoefers C, Mueller-Tidow C, Mueller LP (2015) Cryopreservation does not alter main characteristics of Good Manufacturing Process-grade human multipotent mesenchymal stromal cells including immunomodulating potential and lack of malignant transformation. CYTOTHERAPY, 17: 186-98
Liu X, Weidle K, Schröck K, Tönjes A, Schleinitz D, Breitfeld J, Stumvoll M, Böttcher Y, Schöneberg T, Kovacs P (2015) Signatures of natural selection at the FTO (fat mass and obesity associated) locus in human populations. PLoS One, 10: e0117093
Kumar R, Corbett MA, van Bon BWM, Woenig JA, Weir L, Douglas E, Friend KL, Gardner A, Shaw M, Jolly LA, Tan C, Hunter MF, Hackett A, Field M, Palmer EE, Leffler M, Rogers C, Boyle J, Bienek M, Jensen C, Van Buggenhout G, Van Esch H, Hoffmann K, Raynaud M, Zhao H, Reed R, Hu H, Haas SA, Haan E, Kalscheuer VM, Gecz J (2015) THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability. AMERICAN JOURNAL OF HUMAN GENETICS, 97: 302-10
Komatsuzaki S, Ogawa E, Shimozawa N, Sakamoto O, Haginoya K, Uematsu M, Hasegawa Y, Matsubara Y, Ohura T (2015) First Japanese case of Zellweger syndrome with a mutation in PEX14. PEDIATRICS INTERNATIONAL, 57: 1189-92
Job F, Settele F, Lorey S, Rundfeldt C, Baumann L, Beck-Sickinger AG, Haupts U, Lilie H, Bosse-Doenecke E (2015) Ubiquitin is a versatile scaffold protein for the generation of molecules with de novo binding and advantageous drug-like properties. FEBS OPEN BIO, 5: 579-93
Grünert SC, Wehrle A, Villavicencio-Lorini P, Lausch E, Vetter B, Schwab KO, Tucci S, Spiekerkoetter U (2015) Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening. BMC Medical Genetics, 16: 56
Dutta UR, Hansmann I, Schlote D (2015) Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature. European Journal of Medical Genetics, 58: 154-9
Weber T, Wickenhauser C, Monecke A, Gläser C, Stadler M, Desole M, Ligeti K, Behrmann C, Müller-Tidow C, Müller LP (2014) Treatment of rare co-occurrence of Epstein-Barr virus-driven post-transplant lymphoproliferative disorder and hemophagocytic lymphohistiocytosis after allogeneic stem cell transplantation. Transplant Infectious Disease, 16: 988-92
Thieme T, Patzschke R, Job F, Liebold J, Seemann P, Lilie H, Balbach J, Schwarz E (2014) Biophysical and structural characterization of a folded core domain within the proregion of growth and differentiation factor-5. FEBS Journal, 281: 4866-77
Schulz S, Reichert S, Streetz K, Trautwein C, Reichert Y, Gläser C, Schaller HG, Stein JM (2014) Tumor necrosis factor-α and oral inflammation in patients with Crohn disease. JOURNAL OF PERIODONTOLOGY, 85: 1424-31
Hamann L, Glaeser C, Schulz S, Gross M, Franke A, Nöthlings U, Schumann RR (2014) A micro RNA-146a polymorphism is associated with coronary restenosis. International Journal of Immunogenetics, 41: 393-6
Ezgu F, Krejci P, Li S, de Sousa C, Graham JM, Hansmann I, He W, Porpora K, Wand D, Wertelecki W, Schneider A, Wilcox WR (2014) Phenotype-genotype correlations in patients with Marinesco-Sjögren syndrome. CLINICAL GENETICS, 86: 74-84
Zlomuzica A, Burghoff S, Schrader J, Dere E (2013) Superior working memory and behavioural habituation but diminished psychomotor coordination in mice lacking the ecto-5'-nucleotidase (CD73) gene. Purinergic Signalling, 9: 175-82
Villavicencio-Lorini P, Klopocki E, Trimborn M, Koll R, Mundlos S, Horn D (2013) Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4. EUROPEAN JOURNAL OF HUMAN GENETICS, 21: 743-8
Schulz S, Schlitt A, Lutze A, Lischewski S, Seifert T, Dudakliewa T, Gawe R, Werdan K, Hofmann B, Gläser C, Schaller HG, Reichert S (2013) Genetic variants in TNFα and the one-year cardiovascular outcome in patients with coronary heart disease. INTERNATIONAL JOURNAL OF CARDIOLOGY, 168: 1688-90
Krieger M, Roos A, Stendel C, Claeys KG, Sonmez FM, Baudis M, Bauer P, Bornemann A, de Goede C, Dufke A, Finkel RS, Goebel HH, Häussler M, Kingston H, Kirschner J, Medne L, Muschke P, Rivier F, Rudnik-Schöneborn S, Spengler S, Inzana F, Stanzial F, Benedicenti F, Synofzik M, Lia Taratuto A, Pirra L, Tay SKH, Topaloglu H, Uyanik G, Wand D, Williams D, Zerres K, Weis J, Senderek J (2013) SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome. BRAIN, 136: 3634-44
Heller R, Hoffmann K (2013) Genetische Diagnostik und Beratung bei Arthrogryposis. Medizinische Genetik, Medizinische Genetik (3): 358-364
Hamann L, Koch A, Sur S, Hoefer N, Glaeser C, Schulz S, Gross M, Franke A, Nöthlings U, Zacharowski K, Schumann RR (2013) Association of a common TLR-6 polymorphism with coronary artery disease - implications for healthy ageing? Immunity & Ageing, 10: 43
Grünert SC, Villavicencio-Lorini P, Wermuth B, Lehnert W, Sass JO, Schwab KO (2013) Ornithine transcarbamylase deficiency combined with type 1 diabetes mellitus - a challenge in clinical and dietary management. J Diabetes Metab Disord, 12: 37
Gisselbrecht SS, Barrera LA, Porsch M, Aboukhalil A, Estep PW, Vedenko A, Palagi A, Kim Y, Zhu X, Busser BW, Gamble CE, Iagovitina A, Singhania A, Michelson AM, Bulyk ML (2013) Highly parallel assays of tissue-specific enhancers in whole Drosophila embryos. NATURE METHODS, 10: 774-80
Foja S, Jung M, Harwardt B, Riemann D, Pelz-Ackermann O, Schroeder IS (2013) Hypoxia supports reprogramming of mesenchymal stromal cells via induction of embryonic stem cell-specific microRNA-302 cluster and pluripotency-associated genes. Cellular Reprogramming, 15: 68-79
Dutta UR, Pidugu VK, Goud CV, Hoefers C, Hagemann M, Dalal A (2013) Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development. GENE, 519: 374-80
Ding Z, Burghoff S, Buchheiser A, Kögler G, Schrader J (2013) Survival, integration, and differentiation of unrestricted somatic stem cells in the heart. CELL TRANSPLANTATION, 22: 15-27
De Summa S, Pinto R, Sambiasi D, Petriella D, Paradiso V, Paradiso A, Tommasi S (2013) BRCAness: a deeper insight into basal-like breast tumors. ANNALS OF ONCOLOGY, 24 Suppl 8: viii13-viii21
Burghoff S, Flögel U, Bongardt S, Burkart V, Sell H, Tucci S, Ikels K, Eberhard D, Kern M, Klöting N, Eckel J, Schrader J (2013) Deletion of CD73 promotes dyslipidemia and intramyocellular lipid accumulation in muscle of mice. ARCHIVES OF PHYSIOLOGY AND BIOCHEMISTRY, 119: 39-51
Arélin M, Schulze B, Müller-Myhsok B, Horn D, Diers A, Uhlenberg B, Nürnberg P, Nürnberg G, Becker C, Mundlos S, Lindner TH, Sperling K, Hoffmann K (2013) Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects. EUROPEAN JOURNAL OF HUMAN GENETICS, 21: 367-72
Thomssen C, Wand D (2012) Hereditärer Brustkrebs. ONKOLOGE, 18: 216–223
Schulz S, Schlitt A, Lutze A, Lischewski S, Seifert T, Dudakliewa T, Gawe R, Werdan K, Hofmann B, Gläser C, Schaller HG, Reichert S (2012) The importance of genetic variants in TNFα for periodontal disease in a cohort of coronary patients. JOURNAL OF CLINICAL PERIODONTOLOGY, 39: 699-706
Parthey K, Kornhuber M, Kunze C, Wand D, Nolte KW, Nikolin S, Weis J, Schröder JM (2012) SOX10 mutation with peripheral amyelination and developmental disturbance of axons. MUSCLE & NERVE, 45: 284-90
Ott CE, Hein H, Lohan S, Hoogeboom J, Foulds N, Grünhagen J, Stricker S, Villavicencio-Lorini P, Klopocki E, Mundlos S (2012) Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia. JOURNAL OF MEDICAL GENETICS, 49: 437-41
Morimoto M, Yu Z, Stenzel P, Clewing JM, Najafian B, Mayfield C, Hendson G, Weinkauf JG, Gormley AK, Parham DM, Ponniah U, André JL, Asakura Y, Basiratnia M, Bogdanović R, Bokenkamp A, Bonneau D, Buck A, Charrow J, Cochat P, Cordeiro I, Deschenes G, Fenkçi MS, Frange P, Fründ S, Fryssira H, Guillen-Navarro E, Keller K, Kirmani S, Kobelka C, Lamfers P, Levtchenko E, Lewis DB, Massella L, McLeod DR, Milford DV, Nobili F, Saraiva JM, Semerci CN, Shoemaker L, Stajić N, Stein A, Taha D, Wand D, Zonana J, Lücke T, Boerkoel CF (2012) Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia? Orphanet Journal of Rare Diseases, 7: 70
Graul-Neumann LM, Hoffmann K, Robinson P, Horn D (2012) Progeroide Variante eines Marfan-Syndroms-Eine neue Entität. Medizinische Genetik, 24: 279-283
Flögel U, Burghoff S, van Lent PLEM, Temme S, Galbarz L, Ding Z, El-Tayeb A, Huels S, Bönner F, Borg N, Jacoby C, Müller CE, van den Berg WB, Schrader J (2012) Selective activation of adenosine A2A receptors on immune cells by a CD73-dependent prodrug suppresses joint inflammation in experimental rheumatoid arthritis. Science Translational Medicine, 4: 146ra108
Bönner F, Borg N, Burghoff S, Schrader J (2012) Resident cardiac immune cells and expression of the ectonucleotidase enzymes CD39 and CD73 after ischemic injury. PLoS One, 7: e34730
Strotmann R, Schröck K, Böselt I, Stäubert C, Russ A, Schöneberg T (2011) Evolution of GPCR: change and continuity. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 331: 170-8
Schulz S, Stein JM, Altermann W, Klapproth J, Zimmermann U, Reichert Y, Gläser C, Schaller HG, Reichert S (2011) Single nucleotide polymorphisms in interleukin-1gene cluster and subgingival colonization with Aggregatibacter actinomycetemcomitans in patients with aggressive periodontitis. HUMAN IMMUNOLOGY, 72: 940-6
Romio M, Reinbeck B, Bongardt S, Hüls S, Burghoff S, Schrader J (2011) Extracellular purine metabolism and signaling of CD73-derived adenosine in murine Treg and Teff cells. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 301: C530-9
Reichert S, Stein JM, Klapproth J, Zimmermann U, Reichert Y, Gläser C, Schaller HG, Schulz S (2011) The genetic impact of the Q551R interleukin-4 receptor alpha polymorphism for aggressive or chronic periodontitis and the occurrence of periodontopathic bacteria. ARCHIVES OF ORAL BIOLOGY, 56: 1485-93
Horn P, Cortese-Krott MM, Keymel S, Kumara I, Burghoff S, Schrader J, Kelm M, Kleinbongard P (2011) Nitric oxide influences red blood cell velocity independently of changes in the vascular tone. FREE RADICAL RESEARCH, 45: 653-61
Hoffmann K, Heller R (2011) Uniparental disomies 7 and 14. BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 25: 77-100
Hagen A, Bigl A, Wand D, Klopocki E, Heller R, Siekmeyer M, Siekmeyer W, Kiess W, Merkenschlager A (2011) Combined partial trisomy 11q and partial monosomy 10p in a 19-year-old female patient: phenotypic and genotypic findings. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 155A: 3075-81
Engel KMY, Schröck K, Teupser D, Holdt LM, Tönjes A, Kern M, Dietrich K, Kovacs P, Krügel U, Scheidt HA, Schiller J, Huster D, Brockmann GA, Augustin M, Thiery J, Blüher M, Stumvoll M, Schöneberg T, Schulz A (2011) Reduced food intake and body weight in mice deficient for the G protein-coupled receptor GPR82. PLoS One, 6: e29400
Burghoff S, Schrader J (2011) Secretome of human endothelial cells under shear stress. JOURNAL OF PROTEOME RESEARCH, 10: 1160-9
Buchheiser A, Ebner A, Burghoff S, Ding Z, Romio M, Viethen C, Lindecke A, Köhrer K, Fischer JW, Schrader J (2011) Inactivation of CD73 promotes atherogenesis in apolipoprotein E-deficient mice. CARDIOVASCULAR RESEARCH, 92: 338-47
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 (2011) Faulty initiation of proteoglycan synthesis causes cardiac and joint defects. AMERICAN JOURNAL OF HUMAN GENETICS, 89: 15-27