Citation Impact
Citing Papers
The Xenopus Oocyte as a Surrogate Secretory System The Specificity of Protein Export
1980 StandoutNobel
The lipid composition and biochemistry of freshwater fish
1987 Standout
The β-Thalassemias
1999 Standout
Identification and characterization of a spinal muscular atrophy-determining gene
1995 Standout
Genetic Analysis of Innate Immunity
2006 StandoutNobel
Predicting clinical severity in sickle cell anaemia
2005
The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, βS‐globin gene haplotype, co‐inherited α‐thalassemia trait and Hb F on steady‐state serum bilirubin levels in sickle cell anemia
2005
1 The population genetics of the haemoglobinopathies
1998
6 β-Thalassaemia
1993
The muscular dystrophies
2002 Standout
Phenotype—genotype relationships in monogenic disease: lessons from the thalassaemias
2001
Purification and characterization of a human recombinant T-cell protein-tyrosine-phosphatase from a baculovirus expression system
1991 StandoutNobel
Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia
1995
Regression of extramedullary haemopoiesis and augmentation of fetal haemoglobin concentration during hydroxyurea therapy in β thalassaemia
1998
8 The population genetics of the haemoglobinopathies
1993
Gene Defects in β‐Thalassemia and Their Prenatal Diagnosis
1990
Release of free, redox-active iron in the liver and DNA oxidative damage following phenylhydrazine intoxication
1997
Sickle-cell disease
2010 Standout
Nuclei of Adult Mammalian Somatic Cells Are Directly Reprogrammed to oct-4 Stem Cell Gene Expression by Amphibian Oocytes
2003 StandoutNobel
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
Modulation of the Phenotypic Diversity of Sickle Cell Anemia
1996
A Mild Thalassemia Major Resulting from a Compound Heterozygosity for the IVS-11-1 (G→A) Mutation and the Rare T→C Mutation at the Polyadenylation Site
1991
7 Increased HbF in adult life
1993
The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation
2002 Standout
World distribution of factor V Leiden
1995 Standout
Interpreting neural networks for biological sequences by learning stochastic masks
2022 StandoutNobel
Sickle cell disease in Africa: burden and research priorities
2007
Two different forms of homozygous sickle cell disease occur in Saudi Arabia
1991
Why are some genetic diseases common?
1993
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome
2001 StandoutNobel
8 Prenatal diagnosis and screening of the haemoglobinopathies
1998
The Croonian Lecture, 1976 - Egg cytoplasm and gene control in development
1977 StandoutNobel
Studies of the injection of poly(A)+ protamine mRNA into Xenopus laevis oocytes
1978 StandoutNobel
Chapter 7 Methods for Nuclear Transplantation in Amphibia
1977 StandoutNobel
Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL)
2006 Standout
Injected nuclei in frog oocytes: RNA synthesis and protein exchange
1976 StandoutNobel
Xenopusoocytes reactivate muscle gene transcription in transplanted somatic nuclei independently of myogenic factors
2009 StandoutNobel
The expression of the vitellogenin gene
1976
Vitellogenesis: A Versatile Model for Hormonal Regulation of Gene Expression
1979
Somatic nuclei in amphibian oocytes: evidence for selective gene expression
1977 StandoutNobel
The future of cloning
1999 StandoutNatureNobel
Gene activation in somatic nuclei after injection into amphibian oocytes.
1977 StandoutNobel
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations
1991
Nuclear reprogramming and stem cell creation
2003 StandoutNobel
Sequence analysis of the gamma-globin gene locus from a patient with the deletion form of hereditary persistence of fetal hemoglobin
1990
Purified DNAs are transcribed after microinjection into Xenopus oocytes.
1977 StandoutNobel
The reactivation of developmentally inert 5S genes in somatic nuclei injected into Xenopus oocytes
1981 StandoutNatureNobel
A comparison of Xenopus laevis oocyte and embryo mRNA
1981 StandoutNobel
A Common Human β Globin Splicing Mutation Modeled in Mice
1998 StandoutNobel
Glucocorticoid-stimulated accumulation of mouse mammary tumor virus RNA: increased rate of synthesis of viral RNA.
1977 StandoutNobel
In vitro translation and estradiol-17beta induction of Xenopus laevis vitellogenin messenger RNA.
1976
Nuclear Transplantation in Eggs and Oocytes
1986 StandoutNobel
Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene.
1993 StandoutNobel
Synthesis of Albumin and Malic Enzyme in Wheat‐Germ Lysates and Xenopus laevis Oocytes Programmed with Chicken‐Liver Messenger RNA
1979
Recent Advances in Petroleum Microbiology
2003 Standout
Injected nuclei in frog oocytes: fate, enlargement, and chromatin dispersal
1976 StandoutNobel
A mouse model for beta 0-thalassemia.
1995 StandoutNobel
GENE TRANSFER IN AMPHIBIAN EGGS AND OOCYTES
1981 StandoutNobel
Translation of Xenopus liver messenger RNA in Xenopus oocytes: Vitellogenin synthesis and conversion to yolk platelet proteins
1976
The β-δ crossover leading to the βδ hybrid gene of hemoglobin P-Nilotic is located within 54 base-pairs of the 5′ end of exon 2 or between codons 31 and 50
1987
Actin genes in Xenopus and their developmental control
1985 StandoutNobel
Vitellogenesis and the Vitellogenin Gene Family
1981 Science
The activation of RNA synthesis by somatic nuclei injected into amphibian oocytes
1983 StandoutNobel
Regulation of Oocyte Maturation
1980 StandoutNobel
A method for enucleating oocytes ofXenopus laevis
1977 StandoutNobel
Observations on the levels of Hb A2 in patients with different beta- thalassemia mutations and a delta chain variant
1990
Injected nuclei in frog oocytes provide a living cell system for the study of transcriptional control
1976 StandoutNatureNobel
Works of KD Lanclos being referenced
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
1988
Haplotypes in SS patients from Nigeria; characterization of one atypical βS haplotype no. 19 (Benin) associated with elevated HB F and highGγ levels
1992
Certain Mutations Observed in the 5´ Sequences of the <sup>G</sup>γ- and <sup>A</sup>γ-Globin Genes of β<sup>s</sup> Chromosomes Are Specific for Chromosomes with Major Haplotypes
1991
Haplotype-Specific Sequence Variations in the Locus Control Region (5′ Hypersensitive Sites 2, 3, 4) OF βSChrwosomes
1993
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
1988
Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes
1991
Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya
1987
Isolation of and ribonucleic acid synthesis in nuclei of rat fetal liver
1967
Identical nucleotide sequences of the 3'A gamma globin gene enhancer elements from four different chromosomes
1989
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene
1989
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia
1989
Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes
1991
Direct immunofluorescence and enzyme-linked immunosorbent assays for evaluating organic contaminant degrading bacteria
1998
The Effect of α-Thalassemia on the Level of Hybrid Hemoglobin Variants in Heterozygotes
1986
Translation of hormone-induced messenger RNA in amphibian oocytes: I. Induction by estrogen of messenger RNA encoded for vitellogenic protein in the liver of the male African clawed toad (Xenopus laevis).
1975
Haplotypes and α globin gene analyses in sickle cell anaemia patients from Kenya
1987
Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes
1992