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Mark D. Rollag

Researcher at Thomas Jefferson University

Publications -  60
Citations -  9114

Mark D. Rollag is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Melatonin & Pineal gland. The author has an hindex of 31, co-authored 60 publications receiving 8444 citations. Previous affiliations of Mark D. Rollag include Uniformed Services University of the Health Sciences.

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Action Spectrum for Melatonin Regulation in Humans: Evidence for a Novel Circadian Photoreceptor

TL;DR: The results suggest that, in humans, a single photopigment may be primarily responsible for melatonin suppression, and its peak absorbance appears to be distinct from that of rod and cone cellphotopigments for vision.
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A Novel Human Opsin in the Inner Retina

TL;DR: The unique inner retinal localization of melanopsin suggests that it is not involved in image formation but rather may mediate nonvisual photoreceptive tasks, such as the regulation of circadian rhythms and the acute suppression of pineal melatonin.
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Melanopsin: An opsin in melanophores, brain, and eye.

TL;DR: Melanopsin mRNA is expressed in hypothalamic sites thought to contain deep brain photoreceptors and in the iris, a structure known to be directly photosensitive in amphibians, and expression in retinal and nonretinal tissues suggests a role in vision and nonvisual photoreceptive tasks.
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Melanopsin (Opn4) Requirement for Normal Light-Induced Circadian Phase Shifting

TL;DR: These mice display severely attenuated phase resetting in response to brief pulses of monochromatic light, highlighting the critical role of melanopsin in circadian photoentrainment in mammals.
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Melanopsin Is Required for Non-Image-Forming Photic Responses in Blind Mice

TL;DR: It is observed that mice with both outer-retinal degeneration and a deficiency in melanopsin exhibited complete loss of photoentrainment of the circadian oscillator, pupillary light responses, photic suppression of arylalkylamine-N-acetyltransferase transcript, and acute suppression of locomotor activity by light, indicating the importance of both nonvisual and classical visual photoreceptor systems for nonvisual photic responses in mammals.