Citation Impact
Citing Papers
Gating the Selectivity Filter in ClC Chloride Channels
2003 StandoutScienceNobel
Differential Gene Up-Regulation by Hypoxia-Inducible Factor-1α and Hypoxia-Inducible Factor-2α in HEK293T Cells
2005
Concordant Regulation of Gene Expression by Hypoxia and 2-Oxoglutarate-dependent Dioxygenase Inhibition
2006 StandoutNobel
Genome-wide Association of Hypoxia-inducible Factor (HIF)-1α and HIF-2α DNA Binding with Expression Profiling of Hypoxia-inducible Transcripts
2009 StandoutNobel
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
1992 StandoutNatureNobel
The DNA-damage response in human biology and disease
2009 StandoutNature
Human prion diseases with variant prion protein
1994
Molecular biology and genetics of prion diseases
1994 StandoutNobel
Transgenetic investigations of prion diseases of humans and animals
1993 StandoutNobel
NMR structure of the mouse prion protein domain PrP(121–231)
1996 StandoutNatureNobel
The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist
1991 Nobel
Familial Creutzfeldt-Jakob Disease: Codon 200 Prion Disease in Libyan Jews
1997 StandoutNobel
A new inherited prion disease (PrP‐P105L mutation) showing spastic paraparesis
1993
BIOLOGY AND GENETICS OF PRION DISEASES
1994
A 'unified theory' of prion propagation
1991 Nature
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Expression of Vascular Endothelial Growth Factor Receptor 1 in Bone Marrow-derived Mesenchymal Cells Is Dependent on Hypoxia-inducible Factor 1
2006 StandoutNobel
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome
1989 StandoutNatureNobel
Prion Protein Isoforms, a Convergence of Biological and Structural Investigations
1995 StandoutNobel
Gerstmann‐Sträussler‐Scheinker Disease and the Indiana Kindred
1995
Structural Clues to Prion Replication
1994 StandoutScienceNobel
Genetic and Infectious Prion Diseases
1993
The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
1991 Nobel
Molecular Biology and Genetics of Neurodegenerative Diseases Caused By Prions
1992 StandoutNobel
Pharmacologic and Therapeutic Applications of alpha2-Adrenoceptor Subtypes
1993
Human prion diseases
1994 StandoutNobel
Inherited Prion Diseases and Transmission to Rodents
1995
Asparaginyl Hydroxylation of the Notch Ankyrin Repeat Domain by Factor Inhibiting Hypoxia-inducible Factor
2007 StandoutNobel
SWELL1, a Plasma Membrane Protein, Is an Essential Component of Volume-Regulated Anion Channel
2014 StandoutNobel
Single-strand break repair and genetic disease
2008
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Creutzfeldt‐Jakob disease cosegregates with the codon 178AsnPRNP mutation in families of European origin
1992 Nobel
Familial Creutzfeldt-Jakob disease in Finland: Epidemiological, clinical, pathological and molecular genetic studies
1991 Nobel
Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein.
1996 StandoutNobel
Structure and polymorphism of the mouse prion protein gene.
1994 StandoutNobel
Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments
1997 StandoutNobel
Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.
1994 StandoutNobel
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.
1993 StandoutNobel
Prion protein NMR structure and familial human spongiform encephalopathies
1998 StandoutNobel
Regional mapping of prion proteins in brain.
1992 StandoutNobel
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
Proposed three-dimensional structure for the cellular prion protein.
1994 StandoutNobel
Prion Diseases and Neurodegeneration
1994 StandoutNobel
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.
1991 Nobel
Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus.
1996 StandoutNobel
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform.
1995 StandoutNobel
Cardiovascular Regulation in Mice Lacking α 2 -Adrenergic Receptor Subtypes b and c
1996 StandoutScienceNobel
Molecular Structure and Physiological Function of Chloride Channels
2002
Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease
1997 StandoutNobel
A Transmembrane Form of the Prion Protein in Neurodegenerative Disease
1998 ScienceNobel
Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States
1991
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
Prions
1998 StandoutNobel
Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid.
1992 StandoutNobel
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
Structure of the recombinant full-length hamster prion protein PrP(29–231): The N terminus is highly flexible
1997 StandoutNobel
Molecular cloning of a candidate chicken prion protein.
1992 StandoutNobel
Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains
1996 StandoutNobel
Evidence for synthesis of scrapie prion proteins in the endocytic pathway.
1992 StandoutNobel
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
Experimental transmission of human subacute spongiform encephalopathy to small rodents
1984
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform
1997 StandoutNobel
Inherited prion diseases.
1994 StandoutNobel
Recombinant scrapie-like prion protein of 106 amino acids is soluble
1996 StandoutNobel
Prion protein NMR structure and species barrier for prion diseases
1997 StandoutNobel
Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells.
1993 StandoutNobel
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
1992 StandoutNobel
Determinants of carboxyl-terminal domain translocation during prion protein biogenesis
1994 StandoutNobel
Works of J Warter being referenced
Démence pré-sénile familiale: syndrome de Gerstmann-Sträussler-Scheinker.
1982
Multi-centre, double-blind trial of a novel antispastic agent, tizanidine, in spasticity associated with multiple sclerosis
1988
Gerstmann-Straussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
1992
[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease].
1991
Phenotypic variability of aprataxin gene mutations
2003
Novel muscle chloride channel ( CLCN1 ) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance
1998
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
1999
Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann‐Straussler‐Scheinker syndrome
1990