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Cindy R. Eide

Researcher at University of Minnesota

Publications -  25
Citations -  2031

Cindy R. Eide is an academic researcher from University of Minnesota. The author has contributed to research in topics: Induced pluripotent stem cell & Medicine. The author has an hindex of 13, co-authored 21 publications receiving 1881 citations. Previous affiliations of Cindy R. Eide include Macalester College.

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Transplantation of unrelated donor umbilical cord blood in 102 patients with malignant and nonmalignant diseases: influence of CD34 cell dose and HLA disparity on treatment-related mortality and survival.

TL;DR: There is a high probability of survival in recipients of UCB grafts that are disparate in no more than 2 human leukocyte antigens when the grafts contain at least 1.7 x 10(5) CD34(+) cells per kilogram of recipient's body weight, and graft selection should be based principally on CD34 cell dose when multiple UCB units exist with an HLA disparity of 2 or less.
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Somatic mosaicism in Fanconi anemia: Evidence of genotypic reversion in lymphohematopoietic stem cells

TL;DR: The spontaneous genotypic reversion in a lymphohematopoietic stem cell is demonstrated and the subsequent development of a clonal cytogenetic abnormality in nonrevertant cells suggests that ex vivo correction of hematopoetic stem cells by gene transfer may not be sufficient for providing life-long stable hematOPoiesis in patients with FA.
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Induced Pluripotent Stem Cells from Individuals with Recessive Dystrophic Epidermolysis Bullosa

TL;DR: The potential of RDEB iPS cells to generate autologous hematopoietic grafts and skin cells with the inherent capacity to treat skin and mucosal erosions that typify this genodermatosis is identified.

Blood: Original Article Hematopoietic differentiation of induced pluripotent stem cells from patients with mucopolysaccharidosis type I (Hurler syndrome)

TL;DR: It was found that α-L-iduronidase was not required for stem cell renewal, and that MPS-iPS cells showed lysosomal storage characteristic of MPS IH and could be differentiated to both hematopoietic and nonhematopoetic cells.