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David C. Page

Researcher at Massachusetts Institute of Technology

Publications -  523
Citations -  47344

David C. Page is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Y chromosome & X chromosome. The author has an hindex of 110, co-authored 509 publications receiving 44119 citations. Previous affiliations of David C. Page include Hennepin County Medical Center & University of California, Los Angeles.

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Mouse Autosomal Homolog of DAZ, a Candidate Male Sterility Gene in Humans, Is Expressed in Male Germ Cells before and after Puberty

TL;DR: In testes of wildtype mice, Dazh transcription is detectable 1 day after birth, increases steadily as spermatogonial stem cells appear, plateaus as the first wave of sperMatogenic cells enters meiosis, and is sustained at this level thereafter, suggesting that DazH participates in differentiation, proliferation, or maintenance of germ cell founder populations before, during, and after the pubertal onset of sPermatogenesis.
Journal ArticleDOI

Periodic retinoic acid-STRA8 signaling intersects with periodic germ-cell competencies to regulate spermatogenesis.

TL;DR: It is demonstrated that periodic RA–STRA8 signaling intersects with periodic germ-cell competencies to regulate two distinct, cell-type-specific responses: spermatogonial differentiation and meiotic initiation, and contributes to the prodigious output of spermatozoa and to the elaborate organization of sperMatogenesis.
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Meiotic failure in male mice lacking an X-linked factor

TL;DR: The identification of TEX11 as the first X-encoded meiosis-specific factor in mice is reported, which promotes initiation and/or maintenance of synapsis and formation of crossovers, and may provide a physical link between these two meiotic processes.
Proceedings Article

Multiple Instance Regression

Soumya Ray, +1 more
TL;DR: The goals of this work are to understand the computational complexity of the multiple instance regression task and develop an efficient algorithm that is superior to ordinary multiple regression when applied to multiple instance data sets.
Journal ArticleDOI

Direct reprogramming of fibroblasts into embryonic Sertoli-like cells by defined factors.

TL;DR: The generation of induced embryonic Sertoli-like cells (ieSCs) by ectopic expression of five transcription factors is demonstrated and the role of specific transcription factor combinations in the transition from fibroblasts to ieSCs is characterized and key steps in the process are identified.