Pages that link to "Q60057884"
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The following pages link to Giovanna Cenacchi (Q60057884):
Displaying 50 items.
- TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation (Q28116046) (← links)
- A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function (Q28289677) (← links)
- Differentiation of mesenchymal stem cells derived from pancreatic islets and bone marrow into islet-like cell phenotype (Q28741267) (← links)
- Pituicytoma: Ultrastructural Evidence of a Possible Origin from Folliculo-Stellate Cells of the Adenohypophysis (Q29394674) (← links)
- Esophageal cell proliferation in gastroesophageal reflux disease: clinical-morphological data before and after pantoprazole (Q33413173) (← links)
- Liver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathy (Q33573502) (← links)
- Peripheral neuropathy associated with primary Sjögren's syndrome (Q33732941) (← links)
- Different renal phenotypes in related adult males with Fabry disease with the same classic genotype (Q33906945) (← links)
- A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates. (Q34254547) (← links)
- Molecular mechanisms of CD99-induced caspase-independent cell death and cell-cell adhesion in Ewing's sarcoma cells: actin and zyxin as key intracellular mediators. (Q34325539) (← links)
- Response of human chondrocytes and mesenchymal stromal cells to a decellularized human dermis (Q34538197) (← links)
- Medullocytoma (lipidized medulloblastoma). A cerebellar neoplasm of adults with favorable prognosis. (Q34733288) (← links)
- Medullospheres from DAOY, UW228 and ONS-76 cells: increased stem cell population and proteomic modifications (Q34744495) (← links)
- Effect of omeprazole on symptoms and ultrastructural esophageal damage in acid bile reflux. (Q35011174) (← links)
- Sclerosing paraganglioma of the carotid body: a potential pitfall of malignancy. (Q35582717) (← links)
- XAV939-mediated ARTD activity inhibition in human MB cell lines. (Q35593198) (← links)
- Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure (Q35602263) (← links)
- Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous. Report of nerve biopsy in four cases and review of the literature. (Q35972968) (← links)
- The empowerment of translational research: lessons from laminopathies. (Q36281672) (← links)
- Lipolysis and lipophagy in lipid storage myopathies. (Q36934756) (← links)
- Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. (Q36985097) (← links)
- Activity of synthetic peptides against Chlamydia. (Q37834070) (← links)
- In vitro activity of a partially purified and characterized bark extract of Castanea sativa Mill. (ENC®) against Chlamydia spp. (Q37834775) (← links)
- Bacteria sorting by field-flow fractionation. Application to whole-cell Escherichia coil vaccine strains. (Q38521840) (← links)
- Functional expression of calcium-permeable canonical transient receptor potential 4-containing channels promotes migration of medulloblastoma cells (Q38699927) (← links)
- Wnt activation affects proliferation, invasiveness and radiosensitivity in medulloblastoma. (Q38952766) (← links)
- CD99 suppresses osteosarcoma cell migration through inhibition of ROCK2 activity. (Q39156193) (← links)
- Radiobiologic response of medulloblastoma cell lines: involvement of beta-catenin? (Q39952719) (← links)
- Juvenile dermatomyositis: A report of three cases (Q39990391) (← links)
- Intracellular distribution of beta-catenin in human medulloblastoma cell lines with different degree of neuronal differentiation. (Q40141888) (← links)
- ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy. (Q40837097) (← links)
- Ultrastructural and immunohistochemical contribution to the histogenesis of human cardiac myxoma. (Q41436301) (← links)
- Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function. (Q41608018) (← links)
- A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype. (Q41930624) (← links)
- Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations (Q42449617) (← links)
- An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene. (Q42456828) (← links)
- Satellite cell characterization from aging human muscle. (Q42466179) (← links)
- Mixed tumors, myoepitheliomas, and oncocytomas of the soft tissues are likely members of the same family: a clinicopathologic and ultrastructural study. (Q42514866) (← links)
- Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy (Q42579948) (← links)
- Sleep and cardiovascular phenotype in middle-aged hypocretin-deficient narcoleptic mice. (Q43446139) (← links)
- Meningeal sarcoma with rhabdomyoblastic differentiation: case report (Q43829659) (← links)
- Renal calcium phosphate and oxalate deposition in prolonged vitamin B6 deficiency: studies on a rat model of urolithiasis. (Q43953677) (← links)
- Human immunodeficiency virus (HIV) infection of cell cultures. An ultrastructural and immunocytochemical approach. (Q45359427) (← links)
- The role of ultrastructural examination in storage diseases. (Q46118277) (← links)
- Early-onset dementia with prolonged occipital seizures: an atypical case of Kufs disease. (Q46241229) (← links)
- Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene. (Q46764037) (← links)
- Amyloid deposition as a cause of atrial remodelling in persistent valvular atrial fibrillation. (Q47217880) (← links)
- Sub-Populations of Dermal Skin Fibroblasts Secrete Distinct Extracellular Matrix: Implications for Using Skin Substitutes in the Clinic. (Q47229038) (← links)
- Histological and ultrastructural evaluation of human decellularized matrix as a hernia repair device (Q47296517) (← links)
- Magnetic Labelling of Mesenchymal Stem Cells with Iron-Doped Hydroxyapatite Nanoparticles as Tool for Cell Therapy (Q47420082) (← links)