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The American Journal of Surgical Pathology, ISSN 0147-5185, 04/2018, Volume 42, Issue 4, pp. 553 - 560
Journal Article
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 12/2018, Volume 42, Issue 12, pp. 1653 - 1661
Pseudomyogenic hemangioendothelioma (PHE) is an uncommon, rarely metastasizing vascular neoplasm with predilection to affect young adults. The tumors often... 
FOSB | pseudomyogenic hemangioendothelioma | ACTB | SERPINE1 | SURGERY | NEOPLASM | HEMANGIOMA | HYBRIDIZATION | PATHOLOGY | REARRANGEMENTS | SUBSET | SARCOMA-LIKE HEMANGIOENDOTHELIOMA | T(7/12) | EPITHELIOID SARCOMA | BONE | PERICYTOMA | Hemangioendothelioma | Usage | Young adults | Analysis | Fluorescence in situ hybridization | Genetic aspects | Health aspects | Gene fusion | Index Medicus
Journal Article
American Journal of Surgical Pathology, ISSN 0147-5185, 2018, Volume 42, Issue 4, pp. 553 - 560
Journal Article
Autophagy, ISSN 1554-8627, 06/2015, Volume 11, Issue 6, pp. 881 - 890
WDR45/WIPI4, encoding a WD40 repeat-containing PtdIns(3)P binding protein, is essential for the basal autophagy pathway. Mutations in WDR45 cause the... 
fEPSP, field excitatory postsynaptic potential | SQSTM1, sequestosome-1 | epg, ectopic P granule | neurodegeneration | SENDA, static encephalopathy of childhood with neurodegeneration in adulthood | BPAN, β-propeller protein-associated neurodegeneration | axon swelling | H&E, hematoxylin and eosin | AMC, aminomethylcoumarin | LC3, microtubule-associated protein 1 light chain 3 | NBIA, neurodegeneration with brain iron accumulation | Atg, autophagy-related | rpm, rotations per min | autophagy | ACTB, β-actin | CALB, calbindin | WT, wild type | LTP, long-term potentiation | GFAP, glial fibrillary acid protein | CNS, central nervous system | Ei24, etoposide-induced gene 24 | MBP, myelin basic protein | learning and memory | KO, knockout | RBFOX3, RNA binding protein, fox-1 homolog (C. elegans) 3 | Wdr45/Wipi4 | WDR5/WIPI4, WD repeat domain 45 | DCN, deep cerebellar nuclei | Learning and memory | Axon swelling | Neurodegeneration | Autophagy | BRAIN IRON ACCUMULATION | DEGENERATION | CELL BIOLOGY | TRANSPORT | DISEASE | BASAL AUTOPHAGY | MICE | MUTATIONS | Carrier Proteins - genetics | Learning - physiology | Animals | Axons - metabolism | Mice, Transgenic | Autophagy - physiology | Autophagy - genetics | Neurodegenerative Diseases - metabolism | Mutation - genetics | Homeostasis - genetics | Memory - physiology | Index Medicus
Journal Article
Czech Journal of Animal Science, ISSN 1212-1819, 2017, Volume 62, Issue 10, pp. 426 - 434
Reverse transcription quantitative real-time PCR (RT-qPCR) is widely used to study the relative abundance of mRNA transcripts because of its sensitivity and... 
ACTB gene | RT-qPCR | TBP gene | Transcription stability | AGRICULTURE, DAIRY & ANIMAL SCIENCE | transcription stability | MOUSE | QUANTITATIVE RT-PCR | POLYMERASE-II TRANSCRIPTION | REAL-TIME PCR | QPCR ANALYSIS | NORMALIZATION | SELECTION | HOUSEKEEPING GENES | DATA SETS
Journal Article
The American journal of surgical pathology, ISSN 0147-5185, 4/2018, Volume 42, Issue 4, pp. 553 - 560
ACTB1-GLI1 fusions have been reported as the pathognomonic genetic abnormality defining an unusual subset of actin-positive, perivascular myoid tumors, known... 
SHH | S100 protein | pericytoma | PTCH1 | gastroblastoma | MALAT1 | GLI1 | ACTB
Journal Article
Journal Article
Molecular Pain, ISSN 1744-8069, 9/2014, Volume 10, Issue 1, pp. 55 - 55
Journal Article
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 04/2010, Volume 31, Issue 4, pp. 654 - 664
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