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Nature Communications, ISSN 2041-1723, 06/2017, Volume 8, Issue 1, p. 15772
Journal Article
Journal Article
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, ISSN 1756-9966, 07/2019, Volume 38, Issue 1, pp. 313 - 23
BackgroundBreast cancer is the most common malignancy in women worldwide. Among the breast cancer subtypes, triple-negative breast cancer (TNBC) is the most... 
ZEBRAFISH | HMGA1 | VEGF EXPRESSION | MODEL | FOXM1 | MESENCHYMAL TRANSITION | SIGNATURE | Triple-negative breast cancer | VEGFA | Angiogenesis | OVEREXPRESSION | REGULATOR | GENE | ONCOLOGY | Gene network | PROGRESSION | BASAL | Polymerase chain reaction | Usage | Genetic aspects | Research | Zebra fish
Journal Article
Journal Article
Molecular Genetics and Metabolism Reports, ISSN 2214-4269, 2014, Volume 1, Issue C, pp. 477 - 482
The clinical phenotype of Pseudoxanthoma elasticum (PXE) affected patients, although progressive with age, is very heterogeneous, even in the presence of... 
Pseudoxanthoma elasticum | Methylenetetrahydrofolate reductase | Apolipoprotein E | Cardiovascular | Skin-disease
Journal Article
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 2011, Volume 1812, Issue 7, pp. 782 - 790
Journal Article
Neuro-Oncology, ISSN 1522-8517, 05/2018, Volume 20, Issue 6, pp. 776 - 787
Journal Article
by Jaeger, Veronika K and Tikly, Mohammed and Xu, Dong and Siegert, Elise and Hachulla, Eric and Airò, Paolo and Valentini, Gabriele and Matucci Cerinic, Marco and Distler, Oliver and Cozzi, Franco and Carreira, Patricia and Allanore, Yannick and Müller-Ladner, Ulf and Ananieva, Lidia P and Balbir-Gurman, Alexandra and Distler, Jörg H W and Czirják, Laszlo and Li, Mengtao and Henes, Jörg and Jimenez, Sergio A and Smith, Vanessa and Damjanov, Nemanja and Denton, Christopher P and DelGaldo, Francesco and Saketkoo, Lesley Ann and Walker, Ulrich A and Randone, Silvia Bellando and Bannert, Bettina and Iannone, Florenzo and Maurer, Britta and Jordan, Suzana and Dobrota, Rucsandra and Becker, Mike and Mihai, Carina and Becvarare, Radim and Tomčík, Michal and Bielecka, Otylia Kowal and Gindzienska-Sieskiewicz, Ewa and Karaszewska, Katarzyna and Cutolo, Maurizio and Pizzorni, Carmen and Paolino, Sabrina and Sulli, Alberto and Ruaro, Barbara and Alessandri, Elisa and Riccardi, Antonella and Giacco, Veronica and Messitini, Valentina and Irace, Rosaria and Kedor, Claudia and Casteleyn, Vincent and Hilger, Julia and Hoeppner, Jakob and Rednic, Simona and Szabo, Iulia and Petcu, Ana and Avouac, Jérome and Camelia, Frantz and Desbas, Carole and Vlachoyiannopoulos, P and Montecucco, C and Caporali, Roberto and Cavagna, Lorenzo and Stork, Jiri and Inanc, Murat and Joven, Beatriz E and Novak, Srdan and Anic, Felina and Varju, Cecilia and Minier, Tunde and Chizzolini, Carlo and Allai, Daniela and Kucharz, Eugene J and Kotulska, Anna and Kopec-Medrek, Magdalena and Widuchowska, Malgorzata and Dolnicar, Alenka Sipek and Coleiro, Bernard and Gabrielli, Armando and Manfredi, Lucia and Benfaremo, Devis and Ferrarini, Alessia and Bancel, Dominique Farge and Hij, Adrian and Lansiaux, Pauline and Lazzaroni, Maria Grazia and Hesselstrand, Roger and Wuttge, Dirk and Andréasson, ristofer and Martinovic, Duska and Bozic, Ivona and Radic, Mislav and Braun-Moscovici, Yolanda and Monaco, Andrea Lo and Furini, Federica and Hunzelmann, Nicolas and Moinzadeh, Pia and Pellerito, Raffaele and Caimmi, Cristian and Bertoldo, Eugenia and ... and EUSTAR co-authors
Rheumatology, ISSN 1462-0324, 11/2019
Abstract Objectives Racial factors play a significant role in SSc. We evaluated differences in SSc presentations between white patients (WP), Asian patients... 
Journal Article
2011, First, JIMD Reports, ISBN 9783642177071, Volume 1
Tyrosinemia type I is a genetic disorder characterized by accumulation in the blood and urine of the toxic metabolite succinylacetone (SUAC), not detectable in... 
Human Genetics | Pediatrics | Biomedicine | Human Physiology | Metabolic Diseases | Newborn screening | Tyrosinemiatype I | Succynilacetone
Book Chapter
Astrophysical Journal Letters, ISSN 2041-8205, 2017, Volume 850, Issue 2, pp. 1 - 18
The Advanced LIGO and Advanced Virgo observatories recently discovered gravitational waves from a binary neutron star inspiral. A short gamma-ray burst (GRB)... 
Fysik | Subatomär fysik | Physical Sciences | Subatomic Physics | Naturvetenskap | Natural Sciences
Journal Article
Atherosclerosis, ISSN 0021-9150, 2005, Volume 183, Issue 2, pp. 322 - 328
Oxidized-low density lipoproteins (ox-LDL) and the specific receptor LOX-1 are involved in atherogenesis and atherothrombosis. LOX-1 downregulation is... 
Platelets | Statins | LOX-1 polymorphisms | Oxidized-LDL | oxidized-LDL | CARDIAC & CARDIOVASCULAR SYSTEMS | PLATELET-FUNCTION | RISK | LOX-1 | polymorphisms | platelets | GENE | LDL | statins | NITRIC-OXIDE | OLR1 | PERIPHERAL VASCULAR DISEASE | EXPRESSION
Journal Article
Biochimica et Biophysica Acta - Molecular Basis of Disease, ISSN 0925-4439, 05/2011
GM1 gangliosidosis and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence... 
Life Sciences | Biochemistry, Molecular Biology
Journal Article
Biochimica et Biophysica Acta - Molecular Basis of Disease, ISSN 0925-4439, 05/2011
GM1 gangliosidosis and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence... 
Life Sciences | Biochemistry, Molecular Biology
Journal Article
Biochimica et Biophysica Acta - Molecular Basis of Disease, ISSN 0925-4439, 05/2011
GM1 gangliosidosis and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence... 
Life Sciences | Biochemistry, Molecular Biology
Journal Article
Journal Article