Citation Impact
Citing Papers
Tight and specific lanthanide binding in a de novo TIM barrel with a large internal cavity designed by symmetric domain fusion
2020 StandoutNobel
Structure of calmodulin refined at 2.2 Å resolution
1988 Standout
Molecular Basis of Oculocutaneous Albinism.
1994
Mammary gland Ca2+‐binding (‐dependent) proteins: Identification as calelectrins and calpactin I/p36
1988 StandoutNobel
Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism
2005 Standout
Melanin Pigmentation in Mammalian Skin and Its Hormonal Regulation
2004 Standout
1H nuclear‐magnetic‐resonance studies of the three‐dimensional structure of the cardiotoxin CTXIIb from Naja mossambica mossambica in aqueous solution and comparison with the crystal structures of homologous toxins
1988 StandoutNobel
The quantity of thyroid hormone in human milk is too low to influence plasma thyroid hormone levels in the very preterm infant
2002
Monitoring the purification by high‐performance liquid chromatography of cardiotoxins from Naja mossambica mossambica using phase‐sensitive two‐dimensional nuclear magnetic resonance
1987 StandoutNobel
Molecular Basis of Congenital Hypopigmentary Disorders in Humans: A Review
1997
Strong Amerind/White Sex Bias and a Possible Sephardic Contribution among the Founders of a Population in Northwest Colombia
2000 Standout
Identification of Novel Genes Involved in Congenital Hypothyroidism Using Serial Analysis of Gene Expression
2003
The Etiology of Oculocutaneous Albinism (OCA) Type II: The Pink Protein Modulates the Processing and Transport of Tyrosinase
2002
Balance Performance Among Noninstitutionalized Elderly Women
1989
Porphyrias
2010 Standout
A 122.5-Kilobase Deletion of the P Gene Underlies the High Prevalence of Oculocutaneous Albinism Type 2 in the Navajo Population
2003
Breastfeeding and maternal and infant iodine nutrition
2008
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
Determination of the nuclear‐magnetic‐resonance solution structure of cardiotoxin CTX IIb from Naja mossambica mossambica
1993 StandoutNobel
Strategies for Enhanced Photodynamic Therapy Effects†
2007
Two to Tango: Regulation of Mammalian Iron Metabolism
2010 Standout
Iodine and thyroid hormones during pregnancy and postpartum
2007
P gene mutations associated with oculocutaneous albinism type II (OCA2)
2005
What is the cause of the ageing atrophy?
1988 Standout
Ancestral Founder of Mutation W283X in the Porphobilinogen Deaminase Gene among Acute Intermittent Porphyria Patients
2002
Time-resolved europium(III) luminescence excitation spectroscopy: characterization of calcium-binding sites of calmodulin
1988
Thyroglobulin, the prothyroid hormone: chemistry, synthesis and degradation
1999
Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism
1999
Linkage disequilibrium mapping of complex disease: fantasy or reality?
1998
Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria
2005
Aberrant pH of Melanosomes in Pink-Eyed Dilution (p) Mutant Melanocytes
2000
The Activities-specific Balance Confidence (ABC) Scale
1995 Standout
Crystal structure of human homogentisate dioxygenase.
2000
The Loss of Skeletal Muscle Strength, Mass, and Quality in Older Adults: The Health, Aging and Body Composition Study
2006 Standout
[7] Expression and purification of recombinant adenylyl cyclases in Sf9 cells
1994 StandoutNobel
Human pigmentation genetics: the difference is only skin deep
1998
Complementation of Hypopigmentation in p-Mutant (Pink-Eyed Dilution) Mouse Melanocytes by Normal Human P cDNA, and Defective Complementation by OCA2 Mutant Sequences
1997
Fluorescent indicators for Ca2+based on green fluorescent proteins and calmodulin
1997 StandoutNatureNobel
Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease
2004
Analysis of HGD Gene Mutations in Patients with Alkaptonuria from the United Kingdom: Identification of Novel Mutations
2014
The physical activity scale for the elderly (PASE): Development and evaluation
1993 Standout
Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and Postpartum
2011 Standout
Hydrogen Peroxide: A Signaling Messenger
2006 Standout
Regulation of bovine kidney branched-chain 2-oxoacid dehydrogenase complex by reversible phosphorylation
1984 StandoutNobel
Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells
2010 StandoutNobel
Calmodulin: a versatile calcium mediator protein
1994
Exercise and Physical Activity for Older Adults
2009 Standout
pkCSM: Predicting Small-Molecule Pharmacokinetic and Toxicity Properties Using Graph-Based Signatures
2015 Standout
Multicopper Oxidases and Oxygenases
1996 Standout
Ca2+ binding and conformational change in two series of point mutations to the individual Ca(2+)-binding sites of calmodulin.
1992
Liver disease in erythropoietic protoporphyria: insights and implications for management
2007
The Chemistry of Lanthanides in Biology: Recent Discoveries, Emerging Principles, and Technological Applications
2019
Histochemical and Ultrastructural Changes in Senile Human Skeletal Muscle
1977
Muscle morphology, enzyme activity and muscle strength in elderly men and women
1981
Color and genomic ancestry in Brazilians
2002 Standout
Dynamic redistribution of calmodulin in HeLa cells during cell division as revealed by a GFP-calmodulin fusion protein technique
1999 StandoutNobel
Physiological changes in ageing muscles
1973
Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum
1983 Standout
The refined structure of vitamin D-dependent calcium-binding protein from bovine intestine. Molecular details, ion binding, and implications for the structure of other calcium-binding proteins.
1986
Purification and expression of gCap39. An intracellular and secreted Ca2(+)-dependent actin-binding protein enriched in mononuclear phagocytes.
1990 StandoutNobel
Does mental practice enhance performance?
1994 Standout
Optimization of the Additive CHARMM All-Atom Protein Force Field Targeting Improved Sampling of the Backbone ϕ, ψ and Side-Chain χ1 and χ2 Dihedral Angles
2012 Standout
Purification and properties of pyruvate dehydrogenase phosphatase from bovine heart and kidney
1982
Characterization of Calelectrin, a Ca2+‐Binding Protein Isolated from the Electric Organ of Torpedo marmorata
1985 StandoutNobel
Strong Amerind/White Sex Bias and a Possible Sephardic Contribution among the Founders of a Population in Northwest Colombia
2000 Standout
Pink-eyed Dilution Protein Controls the Processing of Tyrosinase
2002
ACSM Position Stand: Exercise and Physical Activity for Older Adults
1998 Standout
Dioxygen Activation at Mononuclear Nonheme Iron Active Sites: Enzymes, Models, and Intermediates
2004 Standout
Human 67-kDa calelectrin contains a duplication of four repeats found in 35-kDa lipocortins.
1988 StandoutNobel
1H‐NMR studies of calmodulin
1984
Histochemical aspects of five limb muscles in old age An autopsy study
1971
Cadmium-113 nuclear magnetic resonance studies of proteolytic fragments of calmodulin: assignment of strong and weak cation binding sites
1983
Interpretation of europium(III) spectra
2015 Standout
ACSM Position Stand: The Recommended Quantity and Quality of Exercise for Developing and Maintaining Cardiorespiratory and Muscular Fitness, and Flexibility in Healthy Adults
1998 Standout
Three-dimensional structure of calmodulin
1985 StandoutNature
Activatable Photosensitizers for Imaging and Therapy
2010 Standout
Effects of cations on affinity of calmodulin for calcium: ordered binding of calcium ions allows the specific activation of calmodulin-stimulated enzymes. Theoretical approach to study of multiple ligand binding to a macromolecule
1981
Imaging and Photodynamic Therapy: Mechanisms, Monitoring, and Optimization
2010 Standout
Morphology and enzymatic capacity in arm and leg muscles in 78–81 year old men and women
1982
Falls in the elderly.
1988
Human skin pigmentation: melanocytes modulate skin color in response to stress
2007 Standout
Size and strength of the quadriceps muscles of old and young women*
1984
Distinct patterns of bidirectional regulation of mammalian adenylyl cyclases.
1994 StandoutNobel
Two novel annexins from Drosophila melanogaster. Cloning, characterization, and differential expression in development.
1990 StandoutNobel
Management of Thyroid Dysfunction during Pregnancy and Postpartum: An Endocrine Society Clinical Practice Guideline
2012 Standout
Calelectrins are a ubiquitous family of Ca2+-binding proteins purified by Ca2+-dependent hydrophobic affinity chromatography by a mechanism distinct from that of calmodulin
1984 StandoutNobel
The effects of ageing and of cachexia upon skeletal muscle A histopathological study
1969
The Effects of Mental Practice on Walking Balance in an Elderly Population
1989
Are interactions with phospholipids responsible for pharmacological activities of cardiotoxins?
1983
Nuclear magnetic resonance studies on calmodulin: calcium-induced conformational change
1983
Spectroscopic Evidence for the Control of Respiration Prior to Phosphorylation in Hamster Brown Fat Cells
1970 StandoutNobel
[3] Purification of calelectrins
1987 StandoutNobel
Acides ribonucléiques messagers de la glande thyroïde
1968
Inheritance in Erythropoietic Protoporphyria: A Common Wild-Type Ferrochelatase Allelic Variant With Low Expression Accounts for Clinical Manifestation
1999
The Caenorhabditis elegans cell death gene ced-4 encodes a novel protein and is expressed during the period of extensive programmed cell death
1992 StandoutNobel
Works of R Aquaron being referenced
Endemic goiter in Morocco (Skoura-Toundoute areas in the high atlas)
1993
Mutation and Polymorphism Analysis of the Human Homogentisate 1,2-Dioxygenase Gene in Alkaptonuria Patients
1998
Identification of 11 Novel Homogentisate 1,2 Dioxygenase Variants in Alkaptonuria Patients and Establishment of a Novel LOVD-Based HGD Mutation Database
2011
Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic Protoporphyria
1998
Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P gene
1997
Analysis of Alkaptonuria (AKU) Mutations and Polymorphisms Reveals that the CCC Sequence Motif Is a Mutational Hot Spot in the Homogentisate 1,2 Dioxygenase Gene (HGO)
1999
Porphobilinogen deaminase gene in African and Afro-Caribbean ethnic groups: mutations causing acute intermittent porphyria and specific intragenic polymorphisms
2000
African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism
1994
[Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. I. 4 new cases].
1971
Simple, reliable and fast spectrofluorometric method for determination of plasma Verteporfin (Visudyne) levels during photodynamic therapy for choroidal neovascularization.
2002
Thyroglobulin iodoamino acids estimation after digestion with pronase and leucylaminopeptidase
1970
Bioavailability of seaweed iodine in human beings.
2002
Proximal muscular weakness in elderly subjects
1968
Ligand binding to macromolecules: Determination of binding parameters by combined use of ligand buffers and flow dialysis; application to calcium-binding proteins
1980
Metal‐Binding Properties of Calmodulin
1982
Acides ribonucléiques messagers de la glande thyroïde de mouton
1968