Dr. Fulvia Ferrazzi



Organisationseinheit


Nephropathologische Abteilung im Pathologischen Institut
Humangenetisches Institut


Publikationen (Download BibTeX)

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Hauer, N., Popp, B., Taher, L., Vogl, C., Dhandapany, P.S., Büttner, C.,... Thiel, C. (2019). Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature. European journal of human genetics. https://dx.doi.org/10.1038/s41431-019-0362-0
Culemann, S., Grüneboom, A., Nicolás-Ávila, J., Weidner, D., Lämmle, K.F., Rothe, T.,... Krönke, G. (2019). Locally renewing resident synovial macrophages provide a protective barrier for the joint. Nature. https://dx.doi.org/10.1038/s41586-019-1471-1
Hauer, N., Popp, B., Schoeller, E., Schuhmann, S., Heath, K.E., Hisado-Oliva, A.,... Thiel, C. (2018). Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature. Genetics in Medicine, 20(6), 630-638. https://dx.doi.org/10.1038/gim.2017.159
Rath, T., Billmeier, U., Ferrazzi, F., Vieth, M., Ekici, A.B., Neurath, M., & Atreya, R. (2018). Effects of Anti-Integrin Treatment With Vedolizumab on Immune Pathways and Cytokines in Inflammatory Bowel Diseases. Frontiers in Immunology, 9. https://dx.doi.org/10.3389/fimmu.2018.01700
Scheller, U., Pfisterer, K., Uebe, S., Ekici, A.B., Reis, A., Jamra, R., & Ferrazzi, F. (2018). Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability. Bmc Medical Genomics, 11(1). https://dx.doi.org/10.1186/s12920-018-0358-6
Schwab, A., Siddiqui, A., Vazakidou, M.E., Napoli, F., Böttcher, M., Menchicchi, B.,... Ceppi, P. (2018). Polyol pathway links glucose metabolism to the aggressiveness of cancer cells. Cancer Research. https://dx.doi.org/10.1158/0008-5472.CAN-17-2834
Zebrowski, D., Jensen, C.H., Becker, R., Ferrazzi, F., Baun, C., Hvidsten, S.,... Engel, F. (2017). Cardiac injury of the newborn mammalian heart accelerates cardiomyocyte terminal differentiation. Scientific Reports, 7(1), 8362. https://dx.doi.org/10.1038/s41598-017-08947-2
Eisenhut, F., Heim, L., Trump, S., Mittler, S., Sopel, N., Andreev, K.,... Finotto, S. (2017). FAM13A is associated with non-small cell lung cancer (NSCLC) progression and controls tumor cell proliferation and survival. OncoImmunology, 6(1), e1256526. https://dx.doi.org/10.1080/2162402X.2016.1256526
Tawamie, H., Martianov, I., Wohlfahrt, N., Buchert, R., Mengus, G., Uebe, S.,... Abou Jamral, R. (2017). Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly. American Journal of Human Genetics, 100(3), 555-561. https://dx.doi.org/10.1016/j.ajhg.2017.01.032
Klinger, P., Lukassen, S., Ferrazzi, F., Ekici, A.B., Hotfiel, T., Swoboda, B.,... Gelse, K. (2017). PEDF Is Associated with the Termination of Chondrocyte Phenotype and Catabolism of Cartilage Tissue. BioMed Research International, 2017, 7183516. https://dx.doi.org/10.1155/2017/7183516

Zuletzt aktualisiert 2017-15-05 um 05:14