S. Quirk

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Apoptosis of Bovine Granulosa Cells After Serum Withdrawal Is Mediated by Fas Antigen (CD95) and Fas Ligand1

R. Harman, C. L. Hu, R. Cowan, 2001, Biology of reproduction.

dGTP triphosphohydrolase, a unique enzyme confined to members of the family Enterobacteriaceae

S. Quirk, M. Bessman, 1991, Journal of bacteriology.

A site-specific endonuclease and co-conversion of flanking exons associated with the mobile td intron of phage T4.

M. Belfort, D. Bell-Pedersen, S. Quirk, 1989, Gene.

WNT4 is required for normal ovarian follicle development and female fertility

A. Boyer, D. Boerboom, J. Richards, 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Potentiation of Fas-Mediated Apoptosis of Murine Granulosa Cells by Interferon-g, Tumor Necrosis Factor- a, and Cycloheximide*

D. Porter, R. Cowan, S. Quirk, 1998 .

The regulation of uterine tissue factor by estrogen

N. Mackman, S. Quirk, D. Loskutoff, 1995, Endocrine.

Rat uterine stromal cells: thrombin receptor and growth stimulation by thrombin.

S. Quirk, K. Henrikson, Y. Zhang, 1996, Endocrinology.

Increased plasma leptin attenuates adaptive metabolism in early lactating dairy cows.

W. R. Butler, S. Quirk, S. Wesolowski, 2016, The Journal of endocrinology.

Dominant activation of the hedgehog signaling pathway alters development of the female reproductive tract

R. Harman, A. Nikitin, R. Cowan, 2012, Genesis.

Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract

R. Harman, R. Cowan, S. Quirk, 2010 .

Overactivation of hedgehog signaling in the developing Müllerian duct interferes with duct regression in males and causes subfertility.

R. Cowan, S. Quirk, V. Selvaraj, 2017, Reproduction.

The Hedgehog Signaling Pathway in the Mouse Ovary1

R. Harman, R. Cowan, S. Quirk, 2007, Biology of reproduction.

Reduced signaling through the hedgehog pathway in the uterine stroma causes deferred implantation and embryonic loss.

R. Harman, R. Cowan, S. Quirk, 2011, Reproduction.

In vivo imaging reveals an essential role of vasoconstriction in rupture of the ovarian follicle at ovulation

W. Zipfel, Rebecca M. Williams, R. Cowan, 2016, Proceedings of the National Academy of Sciences of the United States of America.

The inconsistent distribution of introns in the T-even phages indicates recent genetic exchanges.

M. Belfort, D. Bell-Pedersen, S. Quirk, 1989, Nucleic acids research.

Ovarian follicular growth and atresia: the relationship between cell proliferation and survival.

R. Harman, R. Cowan, D. A. Porter, 2004, Journal of animal science.

REGULATION OF STEROIDOGENESIS IN BOVINE PREOVULATORY FOLLICLES

S. Quirk, J. E. Fortune, 1988 .

Insulin regulates hepatic leptin receptor expression in early lactating dairy cows.

W. R. Butler, S. Quirk, S. R. Thorn, 2008, American journal of physiology. Regulatory, integrative and comparative physiology.

Apoptosis of bovine ovarian surface epithelial cells by Fas antigen/Fas ligand signaling.

R. Harman, R. Cowan, S. Quirk, 2005, Reproduction.

Progesterone receptor and the cell cycle modulate apoptosis in granulosa cells.

R. Harman, R. Cowan, S. Quirk, 2004, Endocrinology.

Expression and Activity of the Fas Antigen in Bovine Ovarian Follicle Cells1

D. Porter, R. Harman, R. Cowan, 2000, Biology of reproduction.

Relationship of Fas ligand expression and atresia during bovine follicle development.

R. Harman, R. Cowan, D. A. Porter, 2001, Reproduction.

Uterine steroid receptor changes associated with progesterone withdrawal during pregnancy and pseudopregnancy in rabbits.

S. Quirk, W. B. Currie, 1984, Endocrinology.

The growth and differentiation of ovarian follicles during the bovine estrous cycle

S. Quirk, J. E. Fortune, J. Sirois, 1988 .

Expression and Function of Fas Antigen Vary in Bovine Granulosa and Theca Cells During Ovarian Follicular Development and Atresia1

R. Cowan, D. A. Porter, S. Quirk, 2000, Biology of reproduction.

The susceptibility of granulosa cells to apoptosis is influenced by oestradiol and the cell cycle.

R. Harman, R. Cowan, S. Quirk, 2006, The Journal of endocrinology.

Growth and regression of ovarian follicles during the follicular phase of the oestrous cycle in heifers undergoing spontaneous and PGF-2 alpha-induced luteolysis.

S. Quirk, J. E. Fortune, G. Hickey, 1986, Journal of reproduction and fertility.

Fas antigen-mediated apoptosis in human granulosa/luteal cells.

R. Cowan, S. Quirk, S. Joshi, 1995, Biology of reproduction.

Cells responding to hedgehog signaling contribute to the theca of ovarian follicles.

R. Cowan, S. Quirk, 2021, Reproduction.

Cell cycle progression and activation of Akt kinase are required for insulin-like growth factor I-mediated suppression of apoptosis in granulosa cells.

R. Harman, R. Cowan, S. Quirk, 2004, Molecular endocrinology.

Regulation of the phosphoinositide pathway in cultured Sertoli cells from immature rats: effects of follicle-stimulating hormone and fluoride.

S. Quirk, L. Reichert, 1988, Endocrinology.

Role of the cell cycle in regression of the corpus luteum.

R. Harman, R. Cowan, S. Quirk, 2013, Reproduction.

Responsiveness of Mouse Corpora Luteal Cells to Fas Antigen (CD95)-Mediated Apoptosis1

R. Harman, R. Cowan, S. Quirk, 2000, Biology of reproduction.

Overactivation of Hedgehog Signaling Alters Development of the Ovarian Vasculature in Mice1

R. Cowan, S. Quirk, Yi Ren, 2012, Biology of reproduction.

Primary structure of the deoxyguanosine triphosphate triphosphohydrolase-encoding gene (dgt) of Escherichia coli.

S. Quirk, M. Bessman, S. Bhatnagar, 1990, Gene.

Location and molecular cloning of the structural gene for the deoxyguanosine triphosphate triphosphohydrolase of Escherichia coli

L. Gold, S. Bhatnagar, S. Quirk, 1989, Molecular microbiology.

Intron mobility in phage T4 is dependent upon a distinctive class of endonucleases and independent of DNA sequences encoding the intron core: mechanistic and evolutionary implications

D. Bell-Pedersen, S. Quirk, J. Clyman, 1990, Nucleic Acids Res..

Apoptosis : a technical overview.

S. Quirk, 2001, Methods in molecular medicine.

R. Cowan, S. Quirk, S. Huber, 2022 .

Dominant activation of the hedgehog signaling pathway in the ovary alters theca development and prevents ovulation.

R. Harman, R. Cowan, S. Quirk, 2009, Molecular endocrinology.

Multiphoton microscopy as a tool to study ovarian vasculature in vivo

W. Zipfel, Rebecca M. Williams, R. Cowan, 2013 .

Potentiation of Fas-mediated apoptosis of murine granulosa cells by interferon-gamma, tumor necrosis factor-alpha, and cycloheximide.

R. Cowan, D. A. Porter, S. Quirk, 1998, Endocrinology.

Regulation of Fas Antigen (Fas, CD95)-Mediated Apoptosis of Bovine Granulosa Cells by Serum and Growth Factors1

R. Harman, R. Cowan, S. Quirk, 2000, Biology of reproduction.

Plasma concentrations of gonadotrophins, preovulatory follicular development and luteal function associated with bovine follicular fluid-induced delay of oestrus in heifers.

S. Quirk, J. E. Fortune, 1986, Journal of reproduction and fertility.

Susceptibility of ovarian granulosa cells to apoptosis differs in cells isolated before or after the preovulatory LH surge

R. Harman, R. Cowan, D. A. Porter, 2001, Molecular and Cellular Endocrinology.

Commentary: Amhr2-Cre-Mediated Global Tspo Knockout

S. Quirk, D. Stocco, Kanako Morohaku, 2020, Frontiers in Endocrinology.

Intron mobility in the T-even phages: High frequency inheritance of group I introns promoted by intron open reading frames

M. Belfort, D. Bell-Pedersen, S. Quirk, 1989, Cell.

Potentiation of Fas-Mediated Apoptosis of Murine Granulosa Cells by Interferon-γ, Tumor Necrosis Factor-α, and Cycloheximide* * This work was supported by NIH Grant HD-32535.

R. Cowan, D. A. Porter, S. Quirk, 1998, Endocrinology.

Fas antigen-mediated apoptosis of ovarian surface epithelial cells.

R. Cowan, S. Quirk, Sarah H. Huber, 1997, Endocrinology.

Expression of rat thrombin receptor and mutants in the baculovirus-infected insect cell system.

S. Quirk, A. Restivo, K. Henrikson, 1997, Thrombosis research.

Progesterone secretion by granulosa cells from rats with four- or five-day estrous cycles: the development of responses to follicle-stimulating hormone, luteinizing hormone, and testosterone.

S. Quirk, J. E. Fortune, J. Hilbert, 1986, Endocrinology.