Andrea Ballabio professeur d'université italien
Ballabio, Andrea 1957-
Ballabio, Andrea
VIAF ID: 90357489 (Personal)
Permalink: http://viaf.org/viaf/90357489
Preferred Forms
- 100 0 _ ‡a Andrea Ballabio ‡c professeur d'université italien
- 200 _ 1 ‡a Ballabio ‡b , Andrea ‡f <1957- >
-
- 100 1 _ ‡a Ballabio, Andrea
- 100 1 _ ‡a Ballabio, Andrea ‡d 1957-
- 100 1 _ ‡a Ballabio, Andrea ‡d 1957-
4xx's: Alternate Name Forms (10)
5xx's: Related Names (2)
Works
Title | Sources |
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Dissolution of donor-vacancy clusters in heavily doped n-type germanium | |
Dynamics of Hole Singlet-Triplet Qubits with Large g-Factor Differences | |
Fifteenth IIGB meeting: from Genome sequence to funcional analysis and medical applications / organized by Andrea Ballabio and John Guardiola ; meeting coordinator M. Graziella Persico | |
Genetica / E. S. Curtoni ... \et al.! ; con la collaborazione di A. Ballabio e G. Novelli | |
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance | |
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis | |
Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family. | |
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia | |
Lysosomal adaptation: how the lysosome responds to external cues | |
Lysosomal calcium signalling regulates autophagy through calcineurin and TFEB. | |
Lysosomal disorders: from storage to cellular damage | |
Lysosomal fusion and SNARE function are impaired by cholesterol accumulation in lysosomal storage disorders | |
Lysosomal storage diseases: from pathophysiology to therapy. | |
The lysosome as a signaling control center of cellular homeostasis, 2014: | |
Lysosome: regulator of lipid degradation pathways | |
Lysosome signaling controls the migration of dendritic cells. | |
Lysosomes as dynamic regulators of cell and organismal homeostasis | |
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome | |
Mammalian X-chromosome inactivation and the XIST gene | |
Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1 | |
A method to direct sequence cosmid LAWRIST16 clones. | |
MicroRNA target prediction by expression analysis of host genes | |
MiT/TFE factors control ER-phagy via transcriptional regulation of FAM134B | |
Modelling TFE renal cell carcinoma in mice reveals a critical role of WNT signaling | |
Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) | |
Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency | |
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3) | |
Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients, at DNA and protein levels | |
The mouse iduronate sulfatase gene: identification of a novel transcript. | |
The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases | |
Multiple sulfatase deficiency in a Turkish family resulting from a novel mutation | |
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome | |
Napoli lettera a Francesco / Massimo Enrico Milone ; con un'intervista al cardinale Crescenzio Sepe ; e interventi di Andrea Ballabio ... [et al.] | |
Neuronal-Targeted TFEB Accelerates Lysosomal Degradation of APP, Reducing Aβ Generation and Amyloid Plaque Pathogenesis | |
New mutations identified in the ocular albinism type 1 gene | |
New targets for old diseases: lessons from mucolipidosis type II. | |
Nutrient-sensitive transcription factors TFEB and TFE3 couple autophagy and metabolism to the peripheral clock | |
The ocular albinism type 1 (OA1) gene controls melanosome maturation and size. | |
The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells | |
On the primary site of control in the spontaneous development of small-intestinal sucrase-isomaltase after birth | |
Pharmacological enhancement of mutated alpha-glucosidase activity in fibroblasts from patients with Pompe disease | |
Phosphorylation-regulated degradation of the tumor-suppressor form of PED by chaperone-mediated autophagy in lung cancer cells. | |
The phytoestrogen genistein modulates lysosomal metabolism and transcription factor EB (TFEB) activation | |
Principi interne medicine | |
Proteoglycan desulfation determines the efficiency of chondrocyte autophagy and the extent of FGF signaling during endochondral ossification | |
A RANKL-PKCβ-TFEB signaling cascade is necessary for lysosomal biogenesis in osteoclasts | |
The rise and fall of positional cloning? | |
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor. | |
Safety of arylsulfatase A overexpression for gene therapy of metachromatic leukodystrophy. | |
en scientific article | |
Second Harmonic Generation in Germanium Quantum Wells for Nonlinear Silicon Photonics | |
Selective clearance of aberrant tau proteins and rescue of neurotoxicity by transcription factor EB | |
Self-eating in skeletal development: implications for lysosomal storage disorders | |
Signals from the lysosome: a control centre for cellular clearance and energy metabolism | |
Slc7a7 disruption causes fetal growth retardation by downregulating Igf1 in the mouse model of lysinuric protein intolerance | |
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease | |
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics | |
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance | |
STUB1 regulates TFEB-induced autophagy-lysosome pathway. | |
Studies on cross-reacting material to steroid sulphatase in fibroblasts from patients affected by different types of steroid sulphatase deficiency | |
The sulfatase gene family: cross-species PCR cloning using the MOPAC technique | |
Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum | |
Sulfatases and human disease | |
Sulfatases and sulfatase modifying factors: an exclusive and promiscuous relationship | |
Sulfatases are determinants of alveolar formation | |
Sulphatase activities are regulated by the interaction of sulphatase-modifying factor 1 with SUMF2 | |
SUMF1 enhances sulfatase activities in vivo in five sulfatase deficiencies | |
Systemic inflammation and neurodegeneration in a mouse model of multiple sulfatase deficiency | |
Systems medicine and integrated care to combat chronic noncommunicable diseases | |
T. rex attacks the lysosome | |
Tabibi Sabbu | |
Tagging genes with cassette-exchange sites | |
TargetFinder: searching annotated sequence databases for target genes of transcription factors | |
Telencephalic embryonic subtractive sequences: a unique collection of neurodevelopmental genes. | |
TFE3 regulates whole-body energy metabolism in cooperation with TFEB. | |
TFEB at a glance | |
TFEB controls cellular lipid metabolism through a starvation-induced autoregulatory loop | |
TFEB controls vascular development by regulating the proliferation of endothelial cells | |
TFEB induces mitochondrial itaconate synthesis to suppress bacterial growth in macrophages | |
TFEB regulates autophagy: An integrated coordination of cellular degradation and recycling processes | |
TFEB regulates lysosomal exocytosis of tau and its loss of function exacerbates tau pathology and spreading | |
TFEB regulates murine liver cell fate during development and regeneration | |
Transcription factor EB (TFEB) is a new therapeutic target for Pompe disease | |
Transcriptional activation of lysosomal exocytosis promotes cellular clearance | |
Transcriptional and epigenetic regulation of autophagy in aging | |
A transcriptomic study of Williams-Beuren syndrome associated genes in mouse embryonic stem cells | |
TRIM9 is specifically expressed in the embryonic and adult nervous system | |
TRPML1 links lysosomal calcium to autophagosome biogenesis through the activation of the CaMKKβ/VPS34 pathway | |
Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene. | |
What else is in store for autophagy? Exocytosis of autolysosomes as a mechanism of TFEB-mediated cellular clearance in Pompe disease | |
Wilson disease protein ATP7B utilizes lysosomal exocytosis to maintain copper homeostasis. | |
A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm. |