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Journal Article
Italian Journal of Pediatrics, ISSN 1824-7288, 12/2015, Volume 41, Issue S2
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 12/2015, Volume 290, Issue 50, pp. 29769 - 29780
Journal Article
IOP Conference Series: Materials Science and Engineering, ISSN 1757-8981, 02/2019, Volume 471, Issue 9, p. 92063
Conference Proceeding
The FASEB Journal, ISSN 0892-6638, 05/2017, Volume 31, Issue 5, pp. 1856 - 1866
The proresolution lipid mediator lipoxin (LX)A4 bestows protective bioactions on endothelial cells. We examined the impact of LXA4 on transcellular endothelial... 
Signaling | Vascular cell adhesion molecule 1 | Lipoxin A4 | MiRNA | Wounds | Packaging | Tumor necrosis factor-α | Ribonucleic acid--RNA | Endothelial cells | Index Medicus
Journal Article
Clinical Dysmorphology, ISSN 0962-8827, 01/2019, p. 1
Journal Article
Journal of Pediatric Neurosciences, ISSN 1817-1745, 01/2019, Volume 14, Issue 1, pp. 38 - 41
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 12/2017, Volume 1863, Issue 12, pp. 3243 - 3253
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2017, Volume 173, Issue 2, pp. 546 - 549
Baraitser-Winter malformation syndrome (BWMS), Fryns-Aftimos syndrome (FA), and craniofrontofacial syndromes (CFFs) have all been recently proposed to be part... 
acute myeloid leukemia | gene | Baraitser–Winter malformation syndrome | craniofrontofacial syndromes | Fryns–Aftimos syndrome | ACTB | ACTG1 | ACTB gene | ACTG1 gene | Fryns-Aftimos syndrome | FRONTO-FACIAL SYNDROME | CANCER | Baraitser-Winter malformation syndrome | RETARDATION | MALFORMATIONS | COLOBOMA | COSTELLO-SYNDROME | GENETICS & HEREDITY | PTOSIS | MUTATIONS | Translocation, Genetic | Lissencephaly - diagnosis | Genetic Testing | Humans | Intellectual Disability - complications | Leukemia, Myeloid, Acute - etiology | Brain - abnormalities | Intellectual Disability - genetics | Young Adult | Facies | Electrocardiography | Leukemia, Myeloid, Acute - drug therapy | Epilepsy - genetics | Female | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - complications | Craniofacial Abnormalities - genetics | Lissencephaly - complications | Treatment Outcome | Bone Marrow Examination | Epilepsy - complications | Epilepsy - diagnosis | Magnetic Resonance Imaging | Leukemia, Myeloid, Acute - diagnosis | Comparative Genomic Hybridization | Craniofacial Abnormalities - diagnosis | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Abnormalities, Multiple - diagnosis | Intellectual Disability - diagnosis | Lissencephaly - genetics | Mutation | Lymphomas | Missense mutation | Winter | Myeloid leukemia | Leukemia | Chromosome 7 | Lymphatic leukemia | Acute myeloid leukemia | Lymphoma | Mental retardation | Cancer | Index Medicus
Journal Article
ISSN 1083-351X, 2015
Transthyretin (TTR) is an amyloidogenic protein, the amyloidogenic potential of which is enhanced by a number of specific point mutations. The ability to... 
Journal Article
Journal of immunology research, ISSN 2314-8861, 2014, Volume 2014, pp. 696812 - 11
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 06/2019, Volume 34, Issue Supplement_1
Journal Article
Clinical and Translational Gastroenterology, ISSN 2155-384X, 2012, Volume 3, pp. e28 - e28
The role of T lymphocytes in the pathogenesis of Celiac disease (CD) is well established. However, the mechanisms of T-cell involvement remain elusive. Little... 
Journal Article
Brain & Development, ISSN 0387-7604, 2014, Volume 37, Issue 5, pp. 527 - 536
Journal Article
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