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Richard V. Pearse

Brigham and Women's Hospital

ORCID: 0000-0003-3972-1457

Publishes on Alzheimer's disease research and treatments, Neuroinflammation and Neurodegeneration Mechanisms, Bioinformatics and Genomic Networks. 59 papers and 3.2k citations.

59Publications
3.2kTotal Citations

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Top publicationsby citations

A sauvagine/corticotropin-releasing factor receptor expressed in heart and skeletal muscle.
T Kishimoto, Richard V. Pearse, Chung‐Ren Lin et al.|Proceedings of the National Academy of Sciences|1995
Cited by 373Open Access

Corticotropin-releasing factor (CRF) mediates many critical aspects of the physiological response to stress. These effects are elicited by binding to specific high-affinity receptors, which are coupled to guanine nucleotide stimulatory factor (Gs)-response pathways. Recently, a gene encoding a receptor for CRF, expressed in pituitary and the central nervous system (PC-CRF receptor), was isolated and characterized. Here we report the identification and characterization of a second, distinct CRF receptor that is expressed primarily in heart and skeletal muscle and exhibits a specific ligand preference and antagonist sensitivity compared with the PC-CRF receptor. We refer to this second receptor as the heart/muscle (HM)-CRF receptor.

P-Lim, a LIM homeodomain factor, is expressed during pituitary organ and cell commitment and synergizes with Pit-1.
Ingolf Bach, Simon J. Rhodes, Richard V. Pearse et al.|Proceedings of the National Academy of Sciences|1995
Cited by 291Open Access

A pituitary LIM homeodomain factor, P-Lim, is expressed as Rathke's pouch forms and as specific pituitary cell phenotypes are established, suggesting functional roles throughout pituitary development. While selectively expressed in both anterior and intermediate pituitary in mature mice, P-Lim is also transiently expressed in the developing ventral neural cord and brainstem. P-Lim binds to and activates the promoter of the alpha-glycoprotein subunit gene, a marker of early pituitary development, and synergizes with Pit-1 in transcriptional activation of genes encoding terminal differentiation markers. The LIM domain of P-Lim specifically interacts with the Pit-1 POU domain and is required for synergistic interactions with Pit-1, but not for basal transcriptional activation events.