Citation Impact
Citing Papers
Mangiferin: a natural miracle bioactive compound against lifestyle related disorders
2017 Standout
Targeting cell signaling pathways for drug discovery: An old lock needs a new key
2007
Lumacaftor–Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508delCFTR
2015 Standout
Role of ROS and RNS Sources in Physiological and Pathological Conditions
2016 Standout
Therapeutic Roles of Curcumin: Lessons Learned from Clinical Trials
2012 Standout
Rescue of ΔF508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules
2006
Genotype and Phenotype in Cystic Fibrosis
2000
Network pharmacology: the next paradigm in drug discovery
2008 Standout
The muscular dystrophies
2002 Standout
Curcumin as “Curecumin”: From kitchen to clinic
2007 Standout
An Insulin-like Signaling Pathway Affects Both Longevity and Reproduction in Caenorhabditis elegans
1998 StandoutNobel
Regulation of glutathione synthesis
2008 Standout
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
2002 StandoutNobel
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
1997 Standout
Glutaminolysis and Transferrin Regulate Ferroptosis
2015 Standout
Variations on an inhibitory theme: phasic and tonic activation of GABAA receptors
2005 Standout
Intestinal mucosal barrier function in health and disease
2009 Standout
Salacia root, a unique Ayurvedic medicine, meets multiple targets in diabetes and obesity
2008
Mechanisms of drug combinations: interaction and network perspectives
2009 Standout
The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands
1996
Cystic fibrosis genetics: from molecular understanding to clinical application
2014 Standout
Multiplex PCR: advantages, development, and applications.
1994
The role of the nuclear envelope in Emery–Dreifuss muscular dystrophy
2001
Localization studies of rare missense mutations in cystic fibrosis transmembrane conductance regulator (CFTR) facilitate interpretation of genotype-phenotype relationships
2008
Rhinosinusitis in cystic fibrosis: Not a simple story
2008
A Genetic Linkage Study of Bipolar Disorder and 13 Markers on Chromosome 11 Including the D2 Dopamine Receptor
1993
Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases
2008 Standout
Multi‐targeted therapy by curcumin: how spicy is it?
2008
Update on Key Emerging Challenges in Cystic Fibrosis
2014 Standout
Purified NADH-cytochrome b5 reductase is a novel superoxide anion source inhibited by apocynin: sensitivity to nitric oxide and peroxynitrite
2014
Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin
1990 StandoutNobel
The importance of glutathione in human disease
2003 Standout
Neurosteroids: Biosynthesis and Function of These Novel Neuromodulators
2000
Multicomponent therapeutics for networked systems
2005
Diagnosing the decline in pharmaceutical R&D efficiency
2012 Standout
How antibiotics kill bacteria: from targets to networks
2010 Standout
Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays
2000 Standout
Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens-new tools for genetic analysis
1978 Standout
The Drugs Don't Work
2003
Evidence for a Dystrophin Missense Mutation as a Cause of X-Linked Dilated Cardiomyopathy
1997
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
1980 Standout
Adhesion-dependent tyrosine phosphorylation of β-dystroglycan regulates its interaction with utrophin
2000
A Randomized, Pilot Study to Assess the Efficacy and Safety of Curcumin in Patients with Active Rheumatoid Arthritis
2012 Standout
Organization and chromosomal localization of the human platelet-derived endothelial cell growth factor gene.
1991
Containing the Atom: Sociotechnical Imaginaries and Nuclear Power in the United States and South Korea
2009 Standout
Linkage and gene localization of hereditary spherocytosis (HS)
1978
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
The sociology of expectations in science and technology
2006 Standout
Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p
1978
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
2000 Standout
Role of CFTR in Airway Disease
1999
Inflammatory Bowel Disease
2010 Standout
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
An analysis of vertebrate mRNA sequences: intimations of translational control.
1991 Standout
Point-of-Care Diagnostics for Global Health
2008 Standout
The Status of the Gene Map of the Human Chromosomes
1977 Science
The Genetic Defect Causing Huntington’s Disease: Repeated in Other Contexts?
1997
Distinct variants of erythrocyte protein 4.1 inherited in linkage with elliptocytosis and Rh type in three white families
1988 StandoutNobel
Reactive Oxygen Species in Metabolic and Inflammatory Signaling
2018 Standout
A novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemia
1996
Clinical Practice Guideline (Update): Adult Sinusitis
2015 Standout
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein
2001 StandoutNobel
Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family
1985 Standout
The Molecular Basis of a Case of γ-Glutamylcysteine Synthetase Deficiency
1999
Lung Infections Associated with Cystic Fibrosis
2002 Standout
Gene for Arrhythmogenic Right Ventricular Cardiomyopathy With Diffuse Nonepidermolytic Palmoplantar Keratoderma and Woolly Hair (Naxos Disease) Maps to 17q21
1998
Dopamine Receptors: From Structure to Function
1998 Standout
Biological activities of curcumin and its analogues (Congeners) made by man and Mother Nature
2008 Standout
Developing a framework for responsible innovation
2013 Standout
Works of Kaplan Jc being referenced
Rapid and direct detection of the most frequent Mediterranean beta-thalassemic mutations by multiplex allele-specific enzymatic amplification.
1992
Adhalin gene polymorphism
1994
Relationships between nasal potential difference and respiratory function in adults with cystic fibrosis
1998
Increased frequency of cystic fibrosis deltaF508 mutation in bronchiectasis associated with rheumatoid arthritis
1999
Genotype-phenotype relationships in a cohort of adult cystic fibrosis patients
1996
Genomics and medicine: an anticipation.
2000
Report of the committee on the genetic constitution of chromosome 22
1989
Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients.
1997
Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.
1993
[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12].
1976
Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
1993
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy.
2000
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.
1993
Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II
1995