Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

1992 • 1,686 citations

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

1994 • 1,053 citations

Autologous transplantation with peripheral blood mononuclear cells collected after administration of recombinant granulocyte stimulating factor

1993 • 382 citations

The Wiskott-Aldrich syndrome in the United States and Canada (1892–1979)

1980 • 238 citations

T cells of patients with the Wiskott-Aldrich syndrome have a restricted defect in proliferative responses.

1993 • 197 citations

Carrier Detection in X-Linked Agammaglobulinemia by Analysis of X-Chromosome Inactivation

1987 • 159 citations

T cell lines characterize events in the pathogenesis of the Wiskott-Aldrich syndrome.

1992 • 141 citations

Review Lecture: Mechanisms and evolutionary origins of variable X-chromosome activity in mammals

1974 • 140 citations

Molecular Approaches to Analysis of X-Linked Immunodeficiencies

1992 • 139 citations

Isolation and characterization of CD34⁺ hematopoietic stem cells from human peripheral blood by high‐gradient magnetic cell sorting

1993 • 125 citations

Carrier detection in the Wiskott Aldrich syndrome

1988 • 113 citations

Actin polymerization and pseudopod reorganization accompany anti-CD3-induced growth arrest in Jurkat T cells.

1993 • 112 citations

Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection

1980 • 96 citations

ALLELIC EXCLUSION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN PLATELETS AND T LYMPHOCYTES FROM A WISKOTT-ALDRICH SYNDROME CARRIER

1980 • 95 citations

X-Chromosome inactivation in the Wiskott-Aldrich syndrome: A marker for detection of the carrier state and identfication of cell lineages expressing the gene defect

1989 • 94 citations

Carrier detection in typical and atypical X-linked agammaglobulinemia

1988 • 90 citations

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.

1987 • 77 citations

Clonal evolution in acute myeloid leukemia [editorial; comment]

1993 • 73 citations

Nonrandom X chromosome inactivation in natural killer cells from obligate carriers of X-linked severe combined immunodeficiency.

1993 • 61 citations

Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome

1988 • 60 citations

Recombinant human stem cell factor enhances myeloid colony growth from human peripheral blood progenitors

1993 • 23 citations

The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1

1992 • 16 citations

Identification and positive selection of human progenitor/stem cells for bone marrow transplantation.

1992 • 16 citations