Citation Impact
Citing Papers
Hypoxia-inducible factors enhance glutamate signaling in cancer cells
2014 StandoutNobel
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families
1991
Molecular and cellular biology of cholinesterases
1993
Interleukin-17 Family Members and Inflammation
2004 Standout
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31‐q14.3
2010 StandoutNobel
From Monocytes to M1/M2 Macrophages: Phenotypical vs. Functional Differentiation
2014 Standout
Huntington's disease
2007 Standout
Charcot-Marie-Tooth disease type 1A: mutational mechanisms and candidate gene
1993
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
2004 StandoutNature
Genetic instabilities in human cancers
1998 StandoutNature
Parkinson's disease: clinical features and diagnosis
2008 Standout
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease
1992
Ursolic acid: An anti‐ and pro‐inflammatory triterpenoid
2008 Standout
Aberrant methylation of N-methyl-D-aspartate receptor type 2B (NMDAR2B) in non-small cell carcinoma
2011
Nab proteins are essential for peripheral nervous system myelination
2005
Glucose-6-Phosphate Dehydrogenase Deficiency
1991
The molecular control of cell division, differentiation commitment and maturation in haemopoietic cells
1989 StandoutNature
Heat Shock Protein A12B Protects Vascular Endothelial Cells Against Sepsis-Induced Acute Lung Injury in Mice
2017 Standout
Association of the glutamate receptor subunit gene GRIN2B with attention‐deficit/hyperactivity disorder
2006
Concurrent expression of erythroid and renal aquaporin CHIP and appearance of water channel activity in perinatal rats.
1993 StandoutNobel
Molecular Genetics of Huntington’s Disease
1998
Expression of IL-17B in neurons and evaluation of its possible role in the chromosome 5q-linked form of Charcot–Marie–Tooth disease
2002
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
1997 Standout
The p53 tumour suppressor gene
1991 StandoutNature
Methemoglobinemia: Etiology, Pharmacology, and Clinical Management
1999 Standout
Active Gene Repression by the Egr2·NAB Complex during Peripheral Nerve Myelination
2008
Antibodies to myelin protein zero (P0) protein as markers of auto-immune inner ear diseases
2007 StandoutNobel
Primary vs. secondary neoplasia-associated chromosomal abnormalities—balanced rearrangements vs. genomic imbalances?
1996
NF-κB activation
2000
Acetylcholinesterase Inhibitors: Pharmacology and Toxicology
2013 Standout
Tau protein isoforms, phosphorylation and role in neurodegenerative disorders11These authors contributed equally to this work.
2000 Standout
Reduced Penetrance of the Huntington's Disease Mutation
1997
Mesenchymal stem cells as trophic mediators
2006 Standout
Connections with Connexins: the Molecular Basis of Direct Intercellular Signaling
1996 Standout
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
2000
Family history and DNA analysis in patients with suspected Huntington's disease
2000
Six important themes in amyotrophic lateral sclerosis (ALS) research, 1999
2000
Amyotrophic Lateral Sclerosis
2001 Standout
Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q
1993
The N-methyl-D-aspartate receptor type 2A is frequently methylated in human colorectal carcinoma and suppresses cell growth
2007
A Gain-of-Function Mutation of JAK2 in Myeloproliferative Disorders
2005 Standout
Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene
1993
Crystal Structures of a Complexed and Peptide-Free Membrane Protein–Binding Domain: Molecular Basis of Peptide Recognition by PDZ
1996 StandoutNobel
Landscape genetics: combining landscape ecology and population genetics
2003 Standout
Mesenchymal cell-based repair of large, full-thickness defects of articular cartilage.
1994 Standout
Adipocytic cells cultured from marrow have osteogenic potential
1991
Osteogenic differentiation of purified, culture-expanded human mesenchymal stem cells in vitro
1997 Standout
Clustering of aberrations to specific chromosomes in human neoplasms
2009
Clustering of aberrations to specific chromosomes in human neoplasms
2009
Neurodegenerative Tauopathies
2001 Standout
Copper Active Sites in Biology
2014 Standout
Characterization of ameboid microglia isolated from developing mammalian brain
1986 Standout
The Neandertal Progesterone Receptor
2020 StandoutNobel
Therapeutic Benefit of Intravenous Administration of Bone Marrow Stromal Cells After Cerebral Ischemia in Rats
2001 Standout
The Membrane of the Human Neonatal Red Cell
1985
A Century of Alzheimer's Disease
2006 StandoutScience
Platelet-derived growth factor promotes proliferation of erythropoietic progenitor cells in vitro.
1983
IL-17 Family Cytokines and the Expanding Diversity of Effector T Cell Lineages
2007 Standout
Mice Deficient in Cellular Glutathione Peroxidase Show Increased Vulnerability to Malonate, 3-Nitropropionic Acid, and 1-Methyl-4-Phenyl-1,2,5,6-Tetrahydropyridine
2000 Standout
PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein
1996 StandoutScience
The Clonal Evolution of Tumor Cell Populations
1976 StandoutScience
Fused transcript of abl and bcr genes in chronic myelogenous leukaemia
1985 StandoutNature
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
2000
A chromosomal profile of polycythemia vera
1987
Molecular Characterization of Novel Reciprocal Translocation t(6;14) in an Epstein-Barr Virus-Transformed B Cell Precursor
1987 StandoutNobel
Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo
2000 Standout
Exploring the relationship between essential tremor and Parkinson's disease
2006
The Granulocyte-Macrophage Colony-Stimulating Factors
1985 Science
Birth and Death of Bone Cells: Basic Regulatory Mechanisms and Implications for the Pathogenesis and Treatment of Osteoporosis*
2000 Standout
Binding of Neuroligins to PSD-95
1997 StandoutScienceNobel
Platelet-derived growth factor enhances in vitro erythropoiesis via stimulation of mesenchymal cells.
1985
The novel triterpenoid 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid induces apoptosis of human myeloid leukemia cells by a caspase-8-dependent mechanism.
2000
Genetic Dissection of Complex Traits
1994 StandoutScience
The nature and action of granulocyte-macrophage colony stimulating factors
1980
Human Adipose Tissue Is a Source of Multipotent Stem Cells
2002 Standout
The Genetic Defect Causing Huntington’s Disease: Repeated in Other Contexts?
1997
Molecular identification of a major palmitoylated erythrocyte membrane protein containing the src homology 3 motif.
1991
A Germline Variation in the Progesterone Receptor Gene Increases Transcriptional Activity and May Modify Ovarian Cancer Risk
2004
Marrow Stromal Cells as Stem Cells for Nonhematopoietic Tissues
1997 StandoutScience
Production of erythroid-potentiating activity by a human T-lymphoblast cell line.
1980
The Hemopoietic Colony-stimulating Factors
1995
Immature Copper-Zinc Superoxide Dismutase and Familial Amyotrophic Lateral Sclerosis
2009
Embryonic induction - molecular prospects
1987 StandoutNobel
Matrix Metalloproteinases: A Review
1993 Standout
Synthetic gene frequency maps of man and selective effects of climate
1981
Rearrangements in the p53 gene in Philadelphia chromosome positive chronic myelogenous leukemia [see comments]
1989
The biology of platelet-derived growth factor
1986 Standout
Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.
1995
THE BIOCHEMICAL BASIS FOR DISCOLORATION IN FRESH MEAT: A REVIEW
1990
Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
1993 StandoutScience
Potential of biobased materials for food packaging
1999 Standout
Bone Marrow Stromal Stem Cells: Nature, Biology, and Potential Applications
2001 Standout
Works of F. Ajmar being referenced
Effects of fibroblasts on the growth of erythroid progenitor cells in vitro.
1977
Cytogenetic follow-up after bone marrow transplantation for Philadelphia-positive chronic myeloid leukemia
1989
Molecular Analysis of the IT15 Gene in Patients with Apparently ‘Sporadic’ Huntington’s Disease
1996
Congenital hypomyelination due to myelin protein zero Q215X mutation
1999
Clinical and genetic study of essential tremor in the Italian population
2001
Molecular analysis of Philadelphia-negative myeloproliferative syndromes with i(17q)
1989
mRNA distribution in adult human brain of GRIN2B, a N-methyl-d-aspartate (NMDA) receptor subunit
1997
Autosomal dominant Polycystic Kidney Disease: A linkage evaluation of heterogeneity in Italy
1990
Forensic Applications of Molecular Genetic Analysis: An Italian Collaborative Study on Paternity Testing by the Determination of Variable Number of Tandem Repeat DNA Polymorphisms
1991
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant
1995
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease
1994
A Novel Mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease
1999
Fibroblastoid Colony-Forming Cells in Myeloproliferative Disorders
1983
Karyotype evolution in CML: High frequency of translocations other than the Ph
1987
A case of chronic myelogenous leukemia with unusual chromosomal abnormality
1979
Electrophoretic difference between fetal and adult acetylcholinesterase of human red cell membranes
1980
Methemoglobin reductase variability as related to NAD glycohydrolase activity
1974
Marrow colony stimulating activity in chronic myelogenous leukemia.
1981
Absence of haemolytic effects of L-DOPA on transfused G6PD-deficient erythrocytes
1970
Variability of acetylcholinesterase in adult and fetal red cell membranes.
1981
Coincidence between fragile site expression and interstitial deletion of chromosome 11 in a case of myelofibrosis
1983
A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease.
2004
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian families.
1992
Enzyme studies in glucose-6-phosphate dehydrogenase deficient erythrocytes from egyptians, italians, and american negroes (pyrophosphatase, 6-phosphogluconate dehydrogenase, glutamic-oxalacetic transaminase, acid phosphatase, catalase and superoxide dismutase assays)
1973
Influence of riboflavin and of erythrocyte stroma on glutathione reductase activity in normal, glucose 6 phosphate dehydrogenase deficient and low glutathione reductase individuals.
1973
Terminal erythroid differentiation in the K-562 cell line by 1-beta-D-arabinofuranosylcytosine: accompaniment by c-myc messenger RNA decrease.
1986
A SOD1 gene mutation in a patient with slowly progressing familial ALS
1999