• Publications
  • Influence
Defective mammopoiesis, but normal hematopoiesis, in mice with a targeted disruption of the prolactin gene
Prolactin (PRL) has been implicated in numerous physiological and developmental processes. The mouse PRL gene was disrupted by homologous recombination. The mutation caused infertility in femaleExpand
  • 592
  • 22
  • PDF
Identification of a B-1 B cell–specified progenitor
The B-1 subpopulation of B lymphocytes differs phenotypically and functionally from conventional B-2 B cells. B-1 B cells are proposed to derive from a distinct progenitor, but such a population hasExpand
  • 404
  • 18
Causes, consequences, and reversal of immune system aging.
The effects of aging on the immune system are manifest at multiple levels that include reduced production of B and T cells in bone marrow and thymus and diminished function of mature lymphocytes inExpand
  • 357
  • 14
  • PDF
Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta.
Duchenne muscular dystrophy (DMD) is an X-linked, degenerative muscle disease that is exacerbated by secondary inflammation. Here, we characterized the immunological milieu of dystrophic muscle inExpand
  • 220
  • 14
  • PDF
Reduction in the Developmental Potential of Intrathymic T Cell Progenitors with Age1
Current models of thymic involution propose that intrinsic developmental defects in intrathymic T cell precursors do not contribute to age-related declines in thymopoiesis. This premise wasExpand
  • 198
  • 14
B-1 B cell development in the fetus and adult.
Models of hematopoiesis often depict lymphocyte production as a uniform process in which a homogenous population of hematopoietic stem cells (HSCs) generates progenitors from which all types ofExpand
  • 239
  • 10
Helper (CD4(+)) and cytotoxic (CD8(+)) T cells promote the pathology of dystrophin-deficient muscle.
Duchenne muscular dystrophy (DMD) and mdx mouse dystrophy result from mutations in the dystrophin gene. Although these mutations are primarily responsible for the defects that underlie the pathologyExpand
  • 214
  • 9
The ageing immune system: is it ever too old to become young again?
Ageing is accompanied by a decline in the function of the immune system, which increases susceptibility to infections and can decrease the quality of life. The ability to rejuvenate the ageing immuneExpand
  • 348
  • 8
  • PDF
Embryonic day 9 yolk sac and intra-embryonic hemogenic endothelium independently generate a B-1 and marginal zone progenitor lacking B-2 potential
The majority of B lymphocytes in the adult mouse are generated in the bone marrow from hematopoietic stem cells (HSCs) that first appear in the aorta-gonado-mesonephros region of the fetus onExpand
  • 201
  • 7
Aging and cancer resistance in lymphoid progenitors are linked processes conferred by p16Ink4a and Arf.
Lymphoid progenitors exhibit severe growth defects during aging while myelopoiesis is relatively unperturbed. These effects are due in part to the preferential expression of p16(Ink4a) and Arf inExpand
  • 93
  • 7
...
1
2
3
4
5
...