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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

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