Citation Impact
Citing Papers
Diversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome.
1993 StandoutNobel
Clonality of cell populations in refractory anaemia using combined approach of gene loss and X‐linked restriction fragment length polymorphism‐methylation analyses
1991
Prostaglandin synthase 1 gene disruption in mice reduces arachidonic acid-induced inflammation and indomethacin-induced gastric ulceration
1995 StandoutNobel
Locus control regions of mammalian β-globin gene clusters: combining phylogenetic analyses and experimental results to gain functional insights
1997
Stem cells, cancer, and cancer stem cells
2001 StandoutNature
Leukemia and the disruption of normal hematopoiesis
1991
AID Is Required for c-myc/IgH Chromosome Translocations In Vivo
2004 StandoutNobel
Heterogeneity of lineage involvement by trisomy 8 in myelodysplastic syndrome
1995
Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
1997 StandoutNobel
Clonal lymphocytes are detectable in only some cases of MDS
1992
Chromosomal translocations in human cancer
1994 Nature
The tyrosine kinase c-Abl regulates p73 in apoptotic response to cisplatin-induced DNA damage
1999 StandoutNatureNobel
E2F-1 Functions in Mice to Promote Apoptosis and Suppress Proliferation
1996 StandoutNobel
Male–female differences in fertility and blood pressure in ACE-deficient mice
1995 StandoutNatureNobel
X‐chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post‐chemotherapy females
1991
MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation
2002 StandoutNatureNobel
Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene
1991
Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes
1992
Cytogenetic clonality in myelodysplastic syndromes studied with fluorescence in situ hybridization: lineage, response to growth factor therapy, and clone expansion
1993
Thymocyte development is normal in CTLA-4-deficient mice
1997 StandoutNobel
Structure of human immunoglobulin gamma genes: implications for evolution of a gene family
1982 StandoutNobel
Variability of Interchain Binding of Immunoglobulins: Interchain Bridges of Mouse IgG2a and IgG2b
1970 StandoutNatureNobel
Fetal Hemoglobin Variants in Mice
1968 StandoutScienceNobel
Organization of Immunoglobulin Genes: Reiteration Frequency of the Mouse κ Chain Constant Region Gene
1974 StandoutNobel
Activation Of Cellular Oncogenes in Hemopoietic Cells by Chromosome Translocation
1986
Structural Basis for Antigen-Antibody Recognition
1986 StandoutScienceNobel
Die molekularen Grundlagen der Antik�rperbildung
1969
Pathways through Networks of Branched DNA
1970 StandoutScienceNobel
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
The Locus Control Region Is Necessary for Gene Expression in the Human β-Globin Locus but Not the Maintenance of an Open Chromatin Structure in Erythroid Cells
1998
Isolation and characterization of Caenorhabditis elegans DNA sequences homologous to the v-abl oncogene.
1986 StandoutNobel
Missing band 7 membrane protein in two patients with high Na, low K erythrocytes.
1982
Impaired Long-Term Potentiation, Spatial Learning, and Hippocampal Development in fyn Mutant Mice
1992 StandoutScienceNobel
Clonal studies in the myelodysplastic syndrome using X-linked restriction fragment length polymorphisms
1990
Gamma-Beta Thalassemia: A Cause of Hemolytic Disease of the Newborn
1972
A mouse α-globin-related pseudogene lacking intervening sequences
1980 StandoutNatureNobel
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
Mechanism of Antibody Diversity: Germ Line Basis for Variability
1970 Science
Nucleotide Sequences of Human Globin Messenger RNA
1974 StandoutNobel
Gamma thalassemia resulting from the deletion of a gamma-globin gene.
1983
Kit ligand improves in vitro erythropoiesis in myelodysplastic syndrome
1992
The occurrence of different levels of Gγ chain and of the AγT variant of fetal hemoglobin in newborn babies from several countries
1983
Haemoglobin Constant Spring—A Chain Termination Mutant ?
1971 Nature
Two novel arrangements of the human fetal globin genes: Gγ-Gγand Aγ-Aγ
1984 StandoutNobel
Globin Composition and Synthesis of Hemoglobins in Developing Fetal Mice Erythroid Cells
1967 Science
THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN β‐THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS*
1974
Evidence for somatic rearrangement of immunoglobulin genes coding for variable and constant regions.
1976 StandoutNobel
Identification of a human transcription unit affected by the variant chromosomal translocations 2;8 and 8;22 of Burkitt lymphoma.
1989 StandoutNobel
Inactivation of the human beta-globin gene by targeted insertion into the beta-globin locus control region.
1992
Analysis of the β-δ-globin gene loci in normal and hb lepore DNA: Direct determination of gene linkage and intergene distance
1978
The thalassemia syndromes
1978
Initiation of Protein Synthesis at an Unusual Position in an Immunoglobulin Gene?
1972 StandoutScienceNobel
Organization of immunoglobulin heavy chain genes and allelic deletion model.
1978 StandoutNobel
Human immunoglobulin subclasses. Partial amino acid sequence of the constant region of a γ4 chain
1970 StandoutNobel
Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment length polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene
1992
Deletion of immunoglobulin heavy chain genes from expressed allelic chromosome
1980 StandoutNatureNobel
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 Molecular Genetics of Cancer
1987 StandoutScienceNobel
Anomaly in the γ chain heterogeneity of the newborn
1977 Nature
Angiotensin-converting enzyme and male fertility
1998 StandoutNobel
Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene.
1993 StandoutNobel
Evidence for nonclonal hematopoietic progenitor cell populations in bone marrow of patients with myelodysplastic syndromes
1994 StandoutNobel
Evidence of a New Chimericbcr/c-ablmRNA in Patients with Chronic Myelocytic Leukemia and the Philadelphia Chromosome
1985
The chemical heterogeneity of the fetal hemoglobin of black newborn babies and adults: a reevaluation
1981
Correction of a human beta S-globin gene by gene targeting.
1991 StandoutNobel
Cloning Human Fetal γ Globin and Mouse α-Type Globin DNA: Characterization and Partial Sequencing
1978 StandoutScienceNobel
A mouse model for beta 0-thalassemia.
1995 StandoutNobel
Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes.
1986 StandoutNobel
Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction.
1991
Transformation of retinal glia cells into lens phenotype: expression of MP26, a lens plasma membrane antigen.
1983 StandoutNobel
Molecular analysis of spontaneous somatic mutants
1977 StandoutNatureNobel
A Genetic Marker in the Variable Region of Light Chains of Mouse Immunoglobulins
1970 StandoutNobel
High rate of CAD gene amplification in human cells deficient in MLH1 or MSH6
2001 StandoutNobel
Structural organization of the bcr gene and its role in the Ph′ translocation
1985 Nature
Gene Selection in Hemoglobin and in Antibody-Synthesizing Cells
1972 Science
The Heterogeneity of Normal Hb A2‐β Thalassaemia in Greece
1979
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Chromosomes with one, two, three, and four fetal globin genes: molecular and hematologic analysis
1986
The Primary Immunodeficiencies
1984
Variability of Interchain Binding of Immunoglobulins: Interchain Bridges of Mouse IgG1
1970 StandoutNatureNobel
Chapter 5 Problems of Differentiation in the Vertebrate Lens
1970
Somatic generation of antibody diversity
1983 StandoutNatureNobel
The Silent Carrier of Beta Thalassemia
1969
Hemoglobin casper: β 106 (G8) Leu→Pro
1973
Differential control of the synthesis of two hemoglobin β chains in normal mice
1977
Monoclonal antibodies specific for globin chains
1983
Unexpected relationships between four large deletions in the human β-globin gene cluster
1983 StandoutNobel
Elevated blood pressures in mice lacking endothelial nitric oxide synthase
1996 StandoutNobel
Haemoglobin F Port Royal (α2Gγ2, 125Glu → Ala)
1974
A Second Type of Hereditary Persistence of Foetal Haemoglobin in India
1973
Conservation of sequence and structure flanking the mouse and human β-globin loci: The β-globin genes are embedded within an array of odorant receptor genes
1999 StandoutNobel
Is terminal deoxynucleotidyl transferase a somatic mutagen in lymphocytes?
1974 StandoutNatureNobel
Cloning Human Fetal γ Globin and Mouse α-Type Globin DNA: Preparation and Screening of Shotgun Collections
1978 StandoutScienceNobel
Defective Lymphoid Development in Mice Lacking Jak3
1995 StandoutScienceNobel
Nucleotide sequence divergence of mouse immunoglobulin gamma 1 and gamma 2b chain genes and the hypothesis of intervening sequence-mediated domain transfer.
1980 StandoutNobel
Works of E. Kleihauer being referenced
Fetaler und bleibender Blutfarbstoff in Erythrozyten und Erythroblasten von menschlichen Feten und Neugeborenen
1958
The proximal element of the beta globin locus control region is not functionally required in vivo.
1991
bcr rearrangement and translocation of the c-abl oncogene in Philadelphia positive acute lymphoblastic leukemia
1986
Hemoglobin Freiburg: Abnormal Hemoglobin Due to Deletion of a Single Amino Acid Residue
1966 Science
CONGENITAL IMMUNODEFICIENCY AND AGRANULOCYTOSIS (RETICULAR DYSGENESIA)
1977
C-abl and bcr are rearranged in a Ph1-negative CML patient.
1985
Clonal analysis of myelodysplastic syndromes: evidence of multipotent stem cell origin
1989
HemoglobinBibba or α2136Proβ2, an unstable α chain abnormal hemoglobin
1968
[Hemoglobin anomalies in the German population].
1962
Abnormality of erythrocyte membrane protein in a case of congenital stomatocytosis
1977
Studies on the heterogeneity of hemoglobin
1968
Demonstration von fetalem H�moglobin in den Erythrocyten eines Blutausstrichs
1957
Haemoglobins of Adult and Foetal African Elephants
1965 Nature
Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.
1968
Severe combined immunodeficiency (SCID) in man: B cell-negative (B-) SCID patients exhibit an irregular recombination pattern at the JH locus.
1991