Citation Impact
Citing Papers
Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria
2006
The Molecular Genetics of Human Hemoglobin
1984
De novo design of allosterically switchable protein assemblies
2024 StandoutNatureNobel
Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in hominoidea
1989 Standout
Hemoglobin: Structure, Function and Allostery
2020
Porphyrias
2010 Standout
Structure and Function of Suppressor tRNAs in Higher Eukaryote
1990
Clinical application of therapeutic erythrocytapheresis (TEA)
2000
Degradation of the E7 human papillomavirus oncoprotein by the ubiquitin-proteasome system: targeting via ubiquitination of the N-terminal residue
2000 StandoutNobel
Reverse osmosis desalination: Water sources, technology, and today's challenges
2009 Standout
Sickle-cell disease
2010 Standout
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death
1994 Standout
Complementary DNA sequences of two 14.5 kDa subunits of NADH:ubiquinone oxidoreductase from bovine heart mitochondria Completion of the primary structure of the complex?
1992 StandoutNobel
Selenocysteine: the 21st amino acid
1991 Standout
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
Nuclear DNA amounts in angiosperms
1976 Standout
Enzymatic excision of DNA bases damaged by exposure to ionizing radiation or oxidizing agents
1985 StandoutNobel
Gene conversions and their relation to homologous chromosome pairing
1986 StandoutNobel
DNA sequence variation associated with elevated fetal G gamma globin production
1985
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
Demystifying Micro-Credit
2008 Standout
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
1986 StandoutNobel
Genetic Alterations at the Molecular Level in X-Ray Induced ad-3B Mutants of Neurospora crassa
1973
Degradation of Myogenic Transcription Factor MyoD by the Ubiquitin Pathway In Vivo and In Vitro: Regulation by Specific DNA Binding
1998 StandoutNobel
Sickle cell anemia as a syndrome: A review of diagnostic features
1979
Biotechnology of Forest Yield
1983 Science
Dose fractionation, dose rate and iso-effect relationships for normal tissue responses
1982 Standout
Through a Green Lens: The Construction of Customary Environmental Law and Community in Indonesia's Maluku Islands
1994 Standout
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
Nucleotide sequence of 16-kilobase pairs of DNA 5' to the human epsilon-globin gene.
1985 StandoutNobel
The contribution of biomass in the future global energy supply: a review of 17 studies
2003 Standout
The Shape of the Dose-Response Curve for Radiation Carcinogenesis: Extrapolation to Low Doses
1977
Insurgent Collective Action and Civil War in El Salvador
2003 Standout
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia
1984
[17] Construction of specific chromosomal rearrangements in yeast
1983 StandoutNobel
The Cytogenetics of Neurospora
1977
GAMMA-RAY MUTAGENESIS IN BACTERIOPHAGE T4
1976
Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients
1984
Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya
1987
The synthesis of the Gγ and Aγ chains of human fetal hemoglobin in erythroid colonies cultured from peripheral blood BFUe's of normal adults and newborn and of subjects with an Aγ or a Gγ chain abnormal fetal hemoglobin
1980
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
United States Agency for International Development
2011 Standout
The occurrence of different levels of Gγ chain and of the AγT variant of fetal hemoglobin in newborn babies from several countries
1983
Agency for International Development
1978 Standout
Two novel arrangements of the human fetal globin genes: Gγ-Gγand Aγ-Aγ
1984 StandoutNobel
Gene Deletion as the Molecular Basis for the Kenya-Gγ-Hpfh Condition
1983
Protein synthesis elongation factor EF-1 alpha is essential for ubiquitin-dependent degradation of certain N alpha-acetylated proteins and may be substituted for by the bacterial elongation factor EF-Tu.
1994 StandoutNobel
Genetic toxicity of some important epoxides
1981 Standout
Organization of ?-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, ?-thalassemia, and ?-thalassemia-2
1982
Youth Employment in Sub-Saharan Africa: Challenges, Constraints and Opportunities
2016 Standout
Ethnobiology, socio-economics and management of mangrove forests: A review
2008 Standout
Genetic Dissection of Complex Traits
1994 StandoutScience
Monoclonal antibodies and cell surface antigens
1979 StandoutNobel
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G? and A? types of ? chain
1984
The Ratio of the Gγ and Aγ Chains: Variations due to Anomalies at the Molecular Level
1985
(Aγδβ)°‐Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA
1985 StandoutNobel
The chemical heterogeneity of the fetal hemoglobin of black newborn babies and adults: a reevaluation
1981
Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes.
1986 StandoutNobel
Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns.
1986
Degradation of the tumor suppressor protein p53 by the ubiquitin-mediated proteolytic system requires a novel species of ubiquitin-carrier protein, E2
1994 StandoutNobel
Basal and human papillomavirus E6 oncoprotein-induced degradation of Myc proteins by the ubiquitin pathway
1998 StandoutNobel
Clinical diversity of sickle cell anemia: Genetic and cellular modulation of disease severity
1983
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Affinity purification of ubiquitin-protein ligase on immobilized protein substrates. Evidence for the existence of separate NH2-terminal binding sites on a single enzyme.
1990 StandoutNobel
Uniformity of Radiation-induced Mutation Rates among Different Species
1973 Nature
The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease
1982
Alpha chain and gamma chain abnormal hemoglobins in newborn babies: Structural and genetic aspects
1983
Cotranslational amino-terminal processing of cytosolic proteins. Cell-free expression of site-directed mutants of human hemoglobin.
1988
Evergreen Agriculture: a robust approach to sustainable food security in Africa
2010 Standout
A Public Economy Approach to Education: Choice and Co-Production
1991 StandoutNobel
Works of B. B. Webber being referenced
Genetics in Plant Breeding.
1957
Hb CAPA OR α294(G1)ASP→GLYβ2, A Mildly Unstable Variant with an A↠G (Gac↠Ggc) Mutation in Cown 94 of the α1-Globin Gene
1994
Hb Natal or α2(minus Tyr-Arg)β2: A high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr → terminating codon) mutation in codon α140
1988
HB P-Nilotic or α2(βδ)2in a Turkish Family
1987
DOSE-RATE EFFECTS ON INACTIVATION AND MUTATION-INDUCTION IN NEUROSPORA CRASSA.
1967
Hb Cheverly or α2β245(CD4)Phe à Ser in an Elderly Italian Male
1982
Hb Doha or α2β2[X-N-Met-1-(NA1)Val → Glu]; a new β-chain abnormal hemoglobin observed in a Qatari female
1985
Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition
1981
The Identification of Five Rare β-Chain Abnormal Hemoglobins by High Performance Liquid Chromatographic Procedures
1986
?-Thalassemia and the production of different ? chain variants in heterozygotes
1981
Hb S, Hb G-PHILADELPHIA AND α-THALASSEMIA-2 IN A BLACK FAMILY
1980
Hb Chicago or α2136(H19)LEU+METβ2 and A-Gγ-GGMGlobin GWE Arrangewznt in a Black Family
1986
GENETICAL AND BIOCHEMICAL STUDIES OF HISTIDINE-REQUIRING MUTANTS OF NEUROSPORA CRASSA. IV. LINKAGE RELATIONSHIPS OF hist-3 MUTANTS
1965
The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis
1979
The separation of human hemoglobin chains by high pressure liquid chromatography.
1981
Hb F-Tokyo or α2GΓ234(B16) Val→Ile, A Silent Γ Chain Variant Detected by Reverse Phase high Performance Liquid Chromatography
1985
The gamma chain heterogeneity of fetal hemoglobin in black beta- thalassemia and HPFH heterozygotes
1981
The Frequency of theAγTGene in the Presence and Absence of the βsor βCGene in the Black Poplilation of the Southeastern USA
1981
INDUCTION KINETICS AND GENETIC ANALYSIS OF X-RAY-INDUCED MUTATIONS IN THE AD-3 REGION OF NEUROSPORA CRASSA
1965