Peter Maye
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Explore the profile of Peter Maye including associated specialties, affiliations and a list of published articles.
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40
Citations
1425
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Recent Articles
1.
Zhang C, Wang H, Chung Y, Hong S, Olmer M, Swahn H, et al.
Bioinformatics
. 2024 Oct;
40(10).
PMID: 39363499
Summary: vSPACE is a web-based application presenting a spatial representation of scRNAseq data obtained from human articular cartilage by emulating the concept of spatial transcriptomics technology, but virtually. This virtual...
2.
McMullan P, Maye P, Root S, Yang Q, Edie S, Rowe D, et al.
bioRxiv
. 2024 Jul;
PMID: 38948860
Heterotopic ossifications (HOs) are the pathologic process by which bone inappropriately forms outside of the skeletal system. Despite HOs being a persistent clinical problem in the general population, there are...
3.
Zhang C, Wang H, Hong S, Olmer M, Swahn H, Lotz M, et al.
bioRxiv
. 2024 Feb;
PMID: 38370845
Single cell RNA sequencing technology has been dramatically changing how gene expression studies are performed. However, its use has been limited to identifying subtypes of cells by comparing cells' gene...
4.
Wang H, Zhang C, Hong S, Maye P, Rowe D, Shin D
bioRxiv
. 2023 Nov;
PMID: 38014057
Cell-cell communication is crucial in maintaining cellular homeostasis, cell survival and various regulatory relationships among interacting cells. Thanks to recent advances of spatial transcriptomics technologies, we can now explore if...
5.
Moses M, Mullen R, Idowu D, Maye P, Jamin S, Behringer R
Front Cell Dev Biol
. 2022 Oct;
10:1006087.
PMID: 36313563
A transgenic mouse approach using bacterial artificial chromosomes (BAC) was used to identify regulatory regions that direct Müllerian duct expression for and (, also known as ). encodes the receptor...
6.
McMullan P, Maye P, Yang Q, Rowe D, Germain-Lee E
JBMR Plus
. 2022 Jan;
6(1):e10570.
PMID: 35079678
Albright hereditary osteodystrophy (AHO) is caused by heterozygous inactivation of , a complex locus that encodes the alpha-stimulatory subunit of heterotrimeric G proteins (Gsα) in addition to and α due...
7.
Rowe D, Hong S, Zhang C, Shin D, Adams D, Youngstrom D, et al.
Bone
. 2020 Oct;
144:115688.
PMID: 33065355
The IMPC/KOMP program provides the opportunity to screen mice harboring well defined gene-inactivation mutations in a uniform genetic background. The program performs a global tissue phenotyping survey that includes skeletal...
8.
Sharma T, Cotney J, Singh V, Sanjay A, Reichenberger E, Ueki Y, et al.
Bone
. 2020 Mar;
135:115315.
PMID: 32165349
Cherubism is a rare genetic disorder caused primarily by mutations in SH3BP2 resulting in excessive bone resorption and fibrous tissue overgrowth in the lower portions of the face. Bone marrow...
9.
Sinder B, Novak S, Wee N, Basile M, Maye P, Matthews B, et al.
Stem Cells
. 2019 Dec;
38(4):530-541.
PMID: 31859429
Osteogenesis imperfecta (OI) is a genetic disorder most commonly caused by mutations associated with type I collagen, resulting in a defective collagen bone matrix. Current treatments for OI focus on...
10.
Diaz-Hernandez M, Khan N, Trochez C, Yoon T, Maye P, Presciutti S, et al.
J Cell Physiol
. 2019 Dec;
235(6):5241-5255.
PMID: 31840817
Intervertebral disc degeneration (IDD) is a public health dilemma as it is associated with low back and neck pain, a frequent reason for patients to visit the physician. During IDD,...