Citation Impact
Citing Papers
Suppression of Aging in Mice by the Hormone Klotho
2005 StandoutScience
Localization and activity of the SNARE Ykt6 determined by its regulatory domain and palmitoylation
2004 StandoutNobel
TRAPP complexes in membrane traffic: convergence through a common Rab
2010
Selective Uptake of Cytosolic, Peroxisomal, and Plasma Membrane Proteins into the Yeast Lysosome for Degradation
1996 StandoutNobel
Internal protein sequence analysis: Enzymatic digestion for less than 10 μg of protein bound to polyvinylidene difluoride or nitrocellulose membranes
1992
A bit of give and take: the relationship between the extracellular matrix and the developing chondrocyte
2003
Conserved synteny between the Fugu and human PTEN locus and the evolutionary conservation of vertebrate PTEN function
2001 StandoutNobel
Association of klotho gene polymorphism with bone density and spondylosis of the lumbar spine in postmenopausal women
2002
Glycosylation in Cellular Mechanisms of Health and Disease
2006 Standout
Ykt6p, a Prenylated SNARE Essential for Endoplasmic Reticulum-Golgi Transport
1997 StandoutNobel
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development
1997 Standout
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder
2004
Nup358, a Cytoplasmically Exposed Nucleoporin with Peptide Repeats, Ran-GTP Binding Sites, Zinc Fingers, a Cyclophilin A Homologous Domain, and a Leucine-rich Region
1995 StandoutNobel
TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
2003 Standout
Ubiquitin-dependent regulation of COPII coat size and function
2012 StandoutNatureNobel
A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)
2006
TANGO1 Facilitates Cargo Loading at Endoplasmic Reticulum Exit Sites
2009 StandoutNobel
The Adaptor Function of TRAPPC2 in Mammalian TRAPPs Explains TRAPPC2-Associated SEDT and TRAPPC9-Associated Congenital Intellectual Disability
2011
The Novel Zinc Finger-Containing Transcription Factor Osterix Is Required for Osteoblast Differentiation and Bone Formation
2002 Standout
Toward a molecular understanding of skeletal development
1995
Cell Adhesion: The Molecular Basis of Tissue Architecture and Morphogenesis
1996 Standout
The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex
1995 StandoutNobel
The Human ATP-Binding Cassette (ABC) Transporter Superfamily
2001
Fibulin-5/DANCE is essential for elastogenesis in vivo
2002 StandoutNatureNobel
New insights into the function of collagens from genetic analysis
1995
An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
1999
Genetic disorders of the elastic fiber system
2000
Asparagine and Aspartate Hydroxylation of the Cytoskeletal Ankyrin Family Is Catalyzed by Factor-inhibiting Hypoxia-inducible Factor
2010 StandoutNobel
Receptor-mediated protein transport in the early secretory pathway
2007
A MAP Kinase Targeted by Endotoxin and Hyperosmolarity in Mammalian Cells
1994 StandoutScience
Collagens and collagen-related diseases
2001
Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking
2006 StandoutNobel
Human White/Murine ABC8 mRNA Levels Are Highly Induced in Lipid-loaded Macrophages
2000
Lysosome-targeting chimaeras for degradation of extracellular proteins
2020 StandoutNatureNobel
[17] Isolation of integral membrane proteins by phase partitioning with triton X-114
1994
A ubiquitin-like system mediates protein lipidation
2000 StandoutNatureNobel
Protein therapeutics: a summary and pharmacological classification
2007 Standout
SEC23-SEC31 the Interface Plays Critical Role for Export of Procollagen from the Endoplasmic Reticulum
2012 StandoutNobel
Novel Mitochondrial Complex II Isolated from Trypanosoma cruzi Is Composed of 12 Peptides Including a Heterodimeric Ip Subunit
2009 StandoutNobel
Synthesis of Heterobifunctional Protein Fusions Using Copper‐Free Click Chemistry and the Aldehyde Tag
2012 StandoutNobel
Germ-Line Mutational Analysis of the TSC2 Gene in 90 Tuberous-Sclerosis Patients
1998
Atg9 Vesicles Recruit Vesicle-tethering Proteins Trs85 and Ypt1 to the Autophagosome Formation Site
2012 StandoutNobel
Coated pits, coated vesicles, and receptor-mediated endocytosis
1979 StandoutNatureNobel
Yeast α factor is processed from a larger precursor polypeptide: The essential role of a membrane-bound dipeptidyl aminopeptidase
1983 StandoutNobel
Role of Rab GTPases in Membrane Traffic and Cell Physiology
2011
Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin
2011 StandoutNobel
RanGTP-mediated nuclear export of karyopherin α involves its interaction with the nucleoporin Nup153
1997 StandoutNobel
Identification of Two GTP-Binding Proteins in the Chloroplast Protein Import Machinery
1994 StandoutScienceNobel
Nuclear Receptors and Lipid Physiology: Opening the X-Files
2001 StandoutScience
Binding of the von Hippel-Lindau Tumor Suppressor Protein to Elongin B and C
1995 StandoutScienceNobel
Atomic Structure of Acetylcholinesterase from Torpedo californica : A Prototypic Acetylcholine-Binding Protein
1991 StandoutScience
C4orf41 and TTC-15 are mammalian TRAPP components with a role at an early stage in ER-to-Golgi trafficking
2011
Intracellular protein topogenesis
1980 StandoutNobel
The transport of lysosomal enzymes
1977
Bone Development
2000
DAF-16 Target Genes That Control C. elegans Life-Span and Metabolism
2003 StandoutScienceNobel
mRNA binding protein mrnp 41 localizes to both nucleus and cytoplasm
1997 StandoutNobel
A Receptor-Mediated Pathway for Cholesterol Homeostasis
1986 StandoutScienceNobel
Early stages in the yeast secretory pathway are required for transport of carboxypeptidase Y to the vacuole
1982 StandoutNobel
Exploring and Engineering the Cell Surface Interface
2005 StandoutScience
Yeast global transcriptional regulators Sin4 and Rgr1 are components of mediator complex/RNA polymerase II holoenzyme.
1995 StandoutNobel
Mutant defective in processing of an enzyme located in the lysosome-like vacuole of Saccharomyces cerevisiae.
1981
Acetylcholinesterase: inhibition by tetranitromethane and arsenite. Binding of arsenite by tyrosine residues.
1985
Site-specific chemical modification of recombinant proteins produced in mammalian cells by using the genetically encoded aldehyde tag
2009 StandoutNobel
Purification and characterization of a novel species of ubiquitin-carrier protein, E2, that is involved in degradation of non-“N-end rule” protein substrates
1994 StandoutNobel
The GTP-binding protein Ran/TC4 is required for protein import into the nucleus
1993 StandoutNatureNobel
Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation
2018 StandoutNobel
Biogenesis of vacuolar membrane glycoproteins of yeast Saccharomyces cerevisiae.
1990 StandoutNobel
Characterization of an In Vitro Model of Elastic Fiber Assembly
1999
Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis
2018
Isolation of Components of the Chloroplast Protein Import Machinery
1994 StandoutScienceNobel
Enzyme therapy in mannose receptor-null mucopolysaccharidosis VII mice defines roles for the mannose 6-phosphate and mannose receptors
2006
Regulation of Rate of Cartilage Differentiation by Indian Hedgehog and PTH-Related Protein
1996 StandoutScience
Aquaporins in the Kidney: From Molecules to Medicine
2002 StandoutNobel
Crystal and Molecular Structure of a Collagen-Like Peptide at 1.9 Å Resolution
1994 StandoutScience
Solubilization and purification of alpha-mannosidase, a marker enzyme of vacuolar membranes in Saccharomyces cerevisiae.
1988 StandoutNobel
Works of George E. Tiller being referenced
Isolation and characterization of a mammalian homolog of the Drosophila white gene
1997
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
1999
A Recurrent RNA-Splicing Mutation in the SEDL Gene Causes X-Linked Spondyloepiphyseal Dysplasia Tarda
2001
Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3
2017
The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda
2001
Multiple Inositol Polyphosphate Phosphatase: Evolution as a Distinct Group within the Histidine Phosphatase Family and Chromosomal Localization of the Human and Mouse Genes to Chromosomes 10q23 and 19
1999
Marshall Syndrome Associated with a Splicing Defect at the COL11A1 Locus
1998
Enzyme-Replacement Therapy in Mucopolysaccharidosis I
2001
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
1995
Cutis Laxa Arising from Frameshift Mutations in Exon 30 of the Elastin Gene (ELN)
1999
Hydrogenation of Triton X-100 eliminates its fluorescence and ultraviolet light absorption while preserving its detergent properties
1984
An amino acid substitution (Gly853–>Glu) in the collagen alpha 1(II) chain produces hypochondrogenesis.
1992
Increased levels of sialic acid associated with a sialidase deficiency in I-cell disease (mucolipidosis II) fibroblasts
1976
Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia.
1990
9-(5-Carboxypentylamino)-acridine An affinity adsorbent ligand for electrophorus acetylcholinesterase
1980