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Research library — page 60

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RPEP-05521 · 2021

Self-Assembling Peptides: How They're Designed and Used in Medicine

Self-assembling peptides form a diverse range of micro- and nanostructures — including nanofibers, hydrogels, and nanotubes — that serve as platforms for tissue regeneration and drug delivery. By modifying amino acid composition, researchers can mimic biological functions, load both hydrophobic and hydrophilic drugs, and engineer stimuli-responsive release at targeted disease sites. The review highlights that biocompatibility and molecular recognition targeting are among their most significant advantages over conventional delivery systems.

La Manna, Sara; Di Natale, Concetta; Onesto, Valentina; Marasco, Daniela · Review

RPEP-05523 · 2021

IL-4 Makes Immune Cells Release Natural Opioids at Injury Sites for Local Pain Relief

IL-4 via IL-4Rα triggered dose-dependent release of Met-enkephalin, β-endorphin, and dynorphin A from M1 macrophages at injured nerves. Release was Ca2+-dependent via PKA, PI3K, and ryanodine receptors. Pain relief blocked by antibodies to each opioid peptide and all three opioid receptor antagonists.

Labuz, Dominika; Celik, Melih Ö; Seitz, Viola; Machelska, Halina · Animal

RPEP-05525 · 2021

ATLAS Bioassay Discovers Tumor Neoantigens That Help AND Hurt — Critical for Cancer Vaccine Safety

ATLAS identified both stimulatory and inhibitory neoantigens. In B16F10 melanoma, stimulatory neoantigens protected while inhibitory ones accelerated tumor growth and abolished protective vaccine efficacy. Clinical trial: personalized vaccine well-tolerated, 99% antigen immune response rate.

Lam, Hubert; McNeil, Lisa K; Starobinets, Hanna; DeVault, Victoria L; Cohen, Roger B; Twardowski, Przemyslaw; Johnson, Melissa L; Gillison, Maura L; Stein, Mark N; Vaishampayan, Ulka N; DeCillis, Arthur P; Foti, James J; Vemulapalli, Vijetha; Tjon, Emily; Ferber, Kyle; DeOliveira, Daniel B; Broom, Wendy; Agnihotri, Parul; Jaffee, Elizabeth M; Wong, Kwok-Kin; Drake, Charles G; Carroll, Pamela M; Davis, Thomas A; Flechtner, Jessica Baker · Clinical Preclinical

RPEP-05528 · 2021

Anti-Tau Antibody Protects Both Brain and Eyes in Alzheimer's Mouse Model

12A12mAb targeting pathological tau N-terminal fragment improved retinal pathology (APP/Aβ processing, tau phosphorylation, inflammation, synaptic proteins, mitochondrial function, neuronal death) in parallel with hippocampal improvements in Tg2576 AD mice after IV administration.

Latina, Valentina; Giacovazzo, Giacomo; Cordella, Federica; Balzamino, Bijorn Omar; Micera, Alessandra; Varano, Monica; Marchetti, Cristina; Malerba, Francesca; Florio, Rita; Ercole, Bruno Bruni; La Regina, Federico; Atlante, Anna; Coccurello, Roberto; Di Angelantonio, Silvia; Calissano, Pietro; Amadoro, Giuseppina · Animal

RPEP-05533 · 2021

Cyclosporin Peptide Derivatives Reveal How Conformation Controls Membrane Permeability

Cyclosporin O derivatives demonstrated that intramolecular hydrogen bonds and conformational chameleonicity determine membrane permeability and cyclophilin A binding. Conformation-permeability-binding relationships were mapped with PK profiling.

Lee, Dongjae; Lee, Sungjin; Choi, Jieun; Song, Yoo-Kyung; Kim, Min Ju; Shin, Dae-Seop; Bae, Myung Ae; Kim, Yong-Chul; Park, Chin-Ju; Lee, Kyeong-Ryoon; Choi, Jun-Ho; Seo, Jiwon · Preclinical

RPEP-05537 · 2021

Substance P Drives Abnormal Lymphatic Vessel Growth in Dry Eye Disease

SP/NK1R system promotes corneal lymphangiogenesis in DED by upregulating VEGFR3 expression on HDLECs. DED mouse model confirmed NK1R-dependent lymphatic vessel invasion. NK1R antagonism could inhibit pathologic lymphangiogenesis.

Lee, Seok Jae; Im, Sang-Taek; Wu, Jun; Cho, Chang Sik; Jo, Dong Hyun; Chen, Yihe; Dana, Reza; Kim, Jeong Hun; Lee, Sang-Mok · Animal

RPEP-05540 · 2021

Parathyroid Hormone: How This Peptide Controls Calcium, Bone, and Why Testing It Is Tricky

Parathyroid hormone (PTH) is the master regulator of calcium and phosphate balance in the body, acting through three main pathways: increasing calcium reabsorption in the kidneys while blocking phosphate reabsorption, stimulating vitamin D activation to boost calcium absorption from food, and increasing bone resorption to release calcium and phosphate into the blood. Parathyroid diseases can arise from genetic mutations affecting gland formation, hormone synthesis or secretion, or gland destruction. Treatment options range from surgical removal of overactive parathyroid tissue to hormone replacement, vitamin D supplementation, phosphate binders, and receptor activators. The review also highlights that current lab tests for PTH can be inaccurate due to interference from hormone fragments, phosphorylation, and amino acid oxidation.

Leung, Edward Ki Yun · Review

RPEP-05548 · 2021

Dipeptide Hydrogels: The Simplest Self-Assembling Peptide Biomaterials

Dipeptides are the shortest self-assembling peptide motifs capable of hydrogel formation. They create diverse nanostructures with controllable properties and biocompatibility for biomedical applications despite minimal complexity.

Li, Liangchun; Xie, Li; Zheng, Renlin; Sun, Rongqin · Review

RPEP-05549 · 2021

Lipophilic Salts and Lipid Formulations Enable Oral Delivery of Peptide Drug Octreotide

Lipophilic salt forms of octreotide in lipid-based formulations improved enzymatic stability in GI lumen and intestinal membrane permeability, addressing both major barriers to oral peptide delivery.

Li, Peng; Ford, Leigh; Haque, Shadabul; McInerney, Mitchell P; Williams, Hywel D; Scammells, Peter J; Thompson, Philip E; Jannin, Vincent; Porter, Christopher J H; Benameur, Hassan; Pouton, Colin W · Preclinical

RPEP-05550 · 2021

Virus-Like Particles Deliver Peptide Antigens to Fight Cancer in Mice

P22 virus-like particles displaying B-cell epitope peptides (VLP-OVAB) induced antibody titers as high as 5.0 × 10⁵ against the peptide antigen. VLPs displaying T-cell epitope peptides (VLP-OVAT) induced highly effective cross-presentation and strongly activated cytotoxic T lymphocyte (CTL) responses. In mouse tumor models, VLP-OVAT significantly inhibited tumor growth by increasing proportions of CD4+ T cells, CD8+ T cells, and effector memory T cells (TEM) among tumor-infiltrating lymphocytes while lowering the proportion of myeloid-derived suppressor cells (MDSCs) that help tumors evade the immune system.

Li, Wenjing; Jing, Zhe; Wang, Shuqing; Li, Qiyu; Xing, Yutong; Shi, Haobo; Li, Shuang; Hong, Zhangyong · Animal

RPEP-05552 · 2021

Thymosin Alpha-1 Treatment for COVID-19 Shows Different Immune Responses in Men vs Women

Tα1 treatment (1.6 mg SC × 15 days) in 78 COVID-19 patients showed gender-dependent immune responses: males had higher CRP and IL-6 but lower PCT post-treatment. Significant variability in lymphocyte subpopulations between Tα1-treated males and females.

Li, Xin; Liu, Lancong; Yang, Yi; Yang, Xuefeng; Wang, Cencen; Li, Yan; Ge, Yanyan; Shi, Yuxin; Lv, Ping; Zhou, Hua; Luo, Pei; Huang, Shilong · Clinical Trial

RPEP-05555 · 2021

Peptide Neoantigen + TLR Agonist Nanocomplexes Boost Cancer Vaccine Immune Responses

Co-assembled nanocomplexes of neoantigen peptide Adpgk with TLR agonist overcame poor immunogenicity of free peptides, efficiently eliciting high-intensity CTL responses through simultaneous antigen-adjuvant delivery to immune cells.

Liang, Zhaoyuan; Cui, Xinyue; Yang, Liqun; Hu, Qin; Li, Danyang; Zhang, Xiaofei; Han, Lu; Shi, Siwei; Shen, Yurong; Zhao, Weijian; Ju, Qi; Deng, Xiongwei; Wu, Yan; Sheng, Wang · Animal Study

RPEP-05556 · 2021

Reversible Dibromomaleimide Peptide Stapling: Fine-Tuning Helical Peptide Drug Design

Optimized reversible dibromomaleimide stapling of peptides using native Cys/homoCys at i, i+4 positions. Structural analysis revealed conformation-activity relationships for α-helical peptide stabilization targeting protein-protein interactions.

Lindsey-Crosthwait, Ayanna; Rodriguez-Lema, Diana; Walko, Martin; Pask, Christopher M; Wilson, Andrew J · In Vitro

RPEP-05560 · 2021

How Well Can Computers Predict Peptide Binding? Not as Well as We'd Like

Traditional peptide QSAR (quantitative structure-activity relationship) methods can only predict domain-peptide binding affinities at a qualitative or semi-quantitative level — not with full quantitative precision. Using over 20,000 peptide segments interacting with SH3, PDZ, and 14-3-3 protein domains, the researchers found that the upper limit of prediction accuracy was R² = 0.7. Two key factors limit accuracy: the inherent flexibility of peptide structures makes them hard to model computationally, and the experimental affinity measurements themselves introduce significant noise.

Liu, Qian; Lin, Jing; Wen, Li; Wang, Shaozhou; Zhou, Peng; Mei, Li; Shang, Shuyong · Computational

RPEP-05561 · 2021

Peptide-Based Cancer Vaccines: Current Clinical Progress and Combination Strategies

Peptide cancer vaccines targeting TAAs or TSAs via CD8+/CD4+ epitopes have achieved clinical benefits. Adjuvants and nanomaterials improve immune responses. Combination with other therapies shows superior anti-cancer efficacy. Multiple candidates in advanced clinical development.

Liu, Wensi; Tang, Haichao; Li, Luanfeng; Wang, Xiangyi; Yu, Zhaojin; Li, Jianping · Review

RPEP-05562 · 2021

Ultrapotent Cyclic Peptide in Cyclotide Scaffold Blocks Blood Clotting Factor XIIa

Engineered cyclotide containing a Factor XIIa inhibitor loop achieved ultrapotent and selective inhibition of human β-Factor XIIa while maintaining the cyclotide scaffold's proteolytic stability and cell permeability.

Liu, Wenyu; de Veer, Simon J; Huang, Yen-Hua; Sengoku, Toru; Okada, Chikako; Ogata, Kazuhiro; Zdenek, Christina N; Fry, Bryan G; Swedberg, Joakim E; Passioura, Toby; Craik, David J; Suga, Hiroaki · In Vitro

RPEP-05564 · 2021

GLP-1 Drug Exenatide Reverses Liver Fibrosis Through Gene and miRNA Regulation in Gerbils

Exenatide reversed high-fat diet-induced liver fibrosis in gerbils. Integrated mRNA and miRNA expression profiling revealed specific gene and regulatory RNA networks modulated by exenatide, elucidating the molecular mechanisms of GLP-1RA hepatoprotection.

Liu, Yuehuan; Wu, Hongru; Wang, Zhiyuan; Wu, Jiusheng; Ying, Shibo; Huang, Minjie; Li, Youming · Animal Study

RPEP-05565 · 2021

GHRH Agonist MR-409 Protects Brain Cells and Promotes Recovery After Stroke in Mice

MR-409 (5-10 μg/mouse/day SC) reduced mortality, ischemic damage, and hippocampal atrophy in tMCAO stroke mice. Enhanced endogenous neurogenesis and neuroplasticity. Protected neural stem cells from oxygen-glucose deprivation. Mechanism: AKT/CREB and BDNF/TrkB activation.

Liu, Yueyang; Yang, Jingyu; Che, Xiaohang; Huang, Jianhua; Zhang, Xianyang; Fu, Xiaoxiao; Cai, Jialing; Yao, Yang; Zhang, Haotian; Cai, Ruiping; Su, Xiaomin; Xu, Qian; Ren, Fu; Cai, Renzhi; Schally, Andrew V; Zhou, Ming-Sheng · Animal Study

RPEP-05566 · 2021

Traditional Chinese Medicine Compound Treats Rosacea by Reducing LL-37 and Macrophage Inflammation

Paeoniflorin promoted SOCS3 expression and inhibited LPS-induced TLR2 and LL-37 expression through SOCS3-ASK1-p38 cascade in macrophages. Rosacea lesions showed increased LL-37 and CD68+ macrophage infiltration. SOCS3 siRNA reversed PF's effects, confirming the mechanism.

Liu, Zijing; Zhang, Jiawen; Jiang, Peiyu; Yin, Zhi; Liu, Yunyi; Liu, Yixuan; Wang, Xiaoyan; Hu, Liang; Xu, Yang; Liu, Wentao · In Vitro

RPEP-05567 · 2021

LEAP-2: The Body's Natural Ghrelin Blocker Emerges as a Promising Anti-Obesity Target

LEAP-2 acts as both competitive ghrelin antagonist and inverse agonist of constitutive GHS-R1a activity. LEAP-2 increases with feeding/obesity, decreases with fasting/weight loss — inverse to ghrelin. LEAP-2/ghrelin molar ratio fluctuates with energy status and modulates food intake.

Lu, Xuehan; Huang, Lili; Huang, Zhengxiang; Feng, Dandan; Clark, Richard J; Chen, Chen · Review

RPEP-05568 · 2021

Engineering Protease-Resistant Peptides for Better Drug Targeting and Delivery

Comprehensive review of strategies to enhance peptide proteolytic resistance for targeting and intracellular delivery: D-amino acids, cyclization, PEGylation, unnatural amino acids, backbone modifications, and hybrid approaches.

Lucana, Maria C; Arruga, Yolanda; Petrachi, Emilia; Roig, Albert; Lucchi, Roberta; Oller-Salvia, Benjamí · Review

RPEP-05569 · 2021

SGLT2 Inhibitors and GLP-1 Drugs Reduce Gout Risk in Danish Population Study

SGLT2 inhibitors associated with reduced gout risk compared to other antidiabetic medications in a Danish population-based cohort. GLP-1 peptides also showed potential gout risk reduction.

Lund, Lars Christian; Højlund, Mikkel; Henriksen, Daniel Pilsgaard; Hallas, Jesper; Kristensen, Kasper Bruun · Observational

RPEP-05570 · 2021

First Anionic Cathelicidin Discovered: Fights Inflammation and Heals Wounds Without Antimicrobial Activity

TK-CATH: first anionic cathelicidin (net charge -3). No direct antimicrobial activity. Potent anti-inflammatory (inhibited LPS-induced cytokines via MAPK). Promoted wound healing: cytokines, chemokines, growth factors, keratinocyte motility/proliferation, and accelerated full-thickness wound repair in mice.

Luo, Xuanjin; Ouyang, Jianhong; Wang, Yan; Zhang, Minghui; Fu, Lei; Xiao, Ning; Gao, Lianghui; Zhang, Peng; Zhou, Jiang; Wang, Yipeng · Animal Study

RPEP-05571 · 2021

Physical Methods to Boost Oral Peptide Drug Absorption Through the Gut

Physical enhancement methods for oral peptide absorption include ultrasound-mediated permeabilization, intestinal microneedle capsules, iontophoresis (electric field-driven transport), and mechanical mucosal disruption devices.

Luo, Zhi; Paunović, Nevena; Leroux, Jean-Christophe · Review

RPEP-05573 · 2021

GLP-1 Receptor Agonists: Cardiovascular Benefits and Therapeutic Potential Beyond Diabetes

GLP-1RAs provide cardiovascular benefits including atherosclerosis reduction, blood pressure lowering, heart failure protection, and anti-inflammatory effects. These benefits are partly independent of glucose control and weight loss.

Ma, Xiaoxuan; Liu, Zhenghong; Ilyas, Iqra; Little, Peter J; Kamato, Danielle; Sahebka, Amirhossein; Chen, Zhengfang; Luo, Sihui; Zheng, Xueying; Weng, Jianping; Xu, Suowen · Review

RPEP-05574 · 2021

Tumor-Targeting Peptide Helps Deliver Chemotherapy Drug Directly to Breast Cancer in Mice

The tLyP-1-functionalized ferritin nanoparticles (tLyP-1-HFtn-PTX) showed enhanced intracellular delivery and superior cytotoxicity against both SMMC-7721 liver cancer and MDA-MB-231 breast cancer cells compared to unmodified ferritin-PTX. The peptide-decorated nanoparticles also demonstrated better anti-invasion ability and deeper penetration into tumor spheroids. In live mice with breast cancer xenografts, tLyP-1-HFtn-PTX selectively accumulated at tumor sites and displayed higher therapeutic efficacy with lower systemic toxicity. Notably, the tLyP-1 peptide functioned effectively at the N-terminal of ferritin, contrary to the previous assumption that it only works at the C-terminus.

Ma, Yuanmeng; Li, Ruike; Dong, Yixin; You, Chaoqun; Huang, Shenlin; Li, Xun; Wang, Fei; Zhang, Yu · Animal Study

RPEP-05576 · 2021

Thymosin Beta-4: Using Embryonic Development Peptides to Reverse Aging in Adult Organs

TB4, a developmentally essential 43aa secreted peptide, demonstrates multiple cardiac regenerative capabilities via systemic administration in adult organisms. The concept proposes using developmental peptides to reactivate embryonic regenerative programs in aging organs.

Maar, Klaudia; Hetenyi, Roland; Maar, Szabolcs; Faskerti, Gabor; Hanna, Daniel; Lippai, Balint; Takatsy, Aniko; Bock-Marquette, Ildiko · Review

RPEP-05578 · 2021

RGD Peptide-Coated Liposomes Deliver Curcumin Directly to Breast Cancer Cells

RGD peptide-modified liposomes loaded with curcumin (RGD-Lip-Cur) demonstrated significantly greater cytotoxicity against MCF-7 breast cancer cells compared to both unmodified curcumin liposomes and free curcumin. At concentrations of 32, 16, and 4 μg/ml, the RGD-targeted version was significantly more toxic to cancer cells (p<0.05 vs plain liposomes, p<0.01 vs free curcumin). The apoptosis assay showed RGD-Lip-Cur induced 39.6% early apoptosis and 40.2% late apoptosis in cancer cells. The formulation also activated caspase 3/7 (cell death enzymes) significantly more than controls. Importantly, RGD-Lip-Cur showed no significant toxicity to normal cells.

Mahmoudi, Reza; Ashraf Mirahmadi-Babaheidri, Seyedeh; Delaviz, Hamdollah; Fouani, Mohamad Hassan; Alipour, Mohsen; Jafari Barmak, Mehrzad; Christiansen, Gunna; Bardania, Hassan ·

RPEP-05579 · 2021

Current and Emerging Treatments for Fatty Liver Disease Including GLP-1 Drugs

No approved NAFLD-specific pharmacotherapy. Current approaches: lifestyle modification, pioglitazone, vitamin E. Emerging: GLP-1RAs showing promise for liver fat reduction and inflammation. NAFLD affects ~30% of adults, up to 70% of T2DM patients.

Mantovani, Alessandro; Dalbeni, Andrea · Review

RPEP-05580 · 2021

GIP and GLP-1: How Your Gut's Incretin Hormones Control Blood Sugar, Weight, and Heart Health

GIP and GLP-1 have additive effects on insulin secretion, but they differ in key ways: GLP-1 suppresses glucagon and slows stomach emptying while GIP increases glucagon secretion and promotes fat storage in adipose tissue. In type 2 diabetes, GIP's ability to stimulate insulin is severely impaired for largely unknown reasons, while GLP-1's effect is only slightly reduced. Beyond glucose control, GLP-1 at pharmacological doses reduces appetite and body weight. GIP shows similar effects in animal studies but not yet convincingly in humans. Both hormones show beneficial effects on cardiovascular disease and neurodegenerative CNS disorders. The superior efficacy of the GIP/GLP-1 co-agonist tirzepatide over selective GLP-1 agonists has fundamentally changed the perception of GIP from a therapeutically useless hormone to a key drug target.

Nauck, Michael A; Quast, Daniel R; Wefers, Jakob; Pfeiffer, Andreas F H ·

RPEP-05581 · 2021

A Ghrelin Receptor Variant Promotes Fat Storage by Changing How Nutrients Are Partitioned

GhsrQ343X allele alters nutrient partitioning to favor fat storage through constitutive GHSR activity, independent of ghrelin-mediated effects. Demonstrates that GHSR baseline signaling independently regulates metabolic programming.

Marion, Candice; Zizzari, Philippe; Denis, Raphaël G P; Hassouna, Rim; Chebani, Yacine; Leste-Lasserre, Thierry; Doat, Hélène; Le Pen, Gwenaëlle; Cota, Daniela; Noble, Florence; Luquet, Serge; Pantel, Jacques · Animal Study

RPEP-05582 · 2021

PTH and PTHrP Peptide Hormones: Dual Roles in Bone Formation and Breakdown

PTH and PTHrP share amino-terminal domain identity and PTH1R receptor activation but have distinct physiological and pharmacological roles in bone. Intermittent PTH builds bone (anabolic) while continuous PTH breaks it down (catabolic). Genetic models clarify mechanism distinctions.

Martin, T John; Sims, Natalie A; Seeman, Ego · Review

RPEP-05584 · 2021

Why Migraine Drugs Stop Working: Anti-Drug Antibodies May Cause Treatment Resistance

Refractory migraine may result from anti-drug antibody development against biologic treatments including anti-CGRP monoclonal antibodies. Multiple mechanisms of pharmacological refractoriness discussed including immunogenicity, receptor changes, and metabolic tolerance.

Maselis, K; Žekevičiūtė, R; Vaitkus, A · Review

RPEP-05585 · 2021

How GLP-1 Drugs Slow Your Stomach — and Why That Effect Fades Over Time

GLP-1 agonists and analogs work in part by slowing gastric emptying — food stays in the stomach longer, which reduces post-meal blood sugar spikes. However, this gastric slowing effect diminishes with long-acting preparations and with long-term use of short-acting preparations through tachyphylaxis (the body adapts to continuous exposure). Key findings from the reviewed literature: endogenous GLP-1 has a half-life of only 2-3 minutes (destroyed by DPP-IV enzyme). GLP-1 infusion slows gastric emptying and increases gastric volumes. Dual GLP-1/GIP agonists (like tirzepatide) do not appear to retard gastric emptying based on reports at the time of review. The chapter also notes that most studies used the acetaminophen absorption test, which primarily measures liquid gastric emptying in the first hour, while scintigraphy provides more valid measurements.

Maselli, Daniel B; Camilleri, Michael · Review

RPEP-05586 · 2021

GLP-1 Drugs as Neuroprotective Agents for Ischemic Stroke: Evidence Review

GLP-1RAs demonstrate pre-clinical neuroprotective efficacy in multiple ischemic stroke models: reducing infarct size, inflammation, and improving functional outcomes. Established safety and availability position them as practical stroke neuroprotectant candidates.

Maskery, Mark P; Holscher, Christian; Jones, Stephanie P; Price, Christopher I; Strain, W David; Watkins, Caroline L; Werring, David J; Emsley, Hedley Ca · Systematic Review

RPEP-05587 · 2021

Network Meta-Analysis Ranks Anti-CGRP Migraine Drugs: Fremanezumab Best at 6 Weeks, Erenumab at 12

At 6 weeks: fremanezumab 900mg most effective (SMD=-0.55). At 8 weeks: erenumab 140mg most effective (SMD=-0.51). At 12 weeks: erenumab 140mg most effective (SMD=-0.48). For chronic migraine: fremanezumab 900mg best at 6 weeks, erenumab 140mg best at 8 and 12 weeks.

Masoud, Ahmed Taher; Hasan, Mohammed Tarek; Sayed, Ahmed; Edward, Harvey Nabil; Amer, Ahmed Mohamed; Naga, Abdelrahman Elshahat; Elfil, Mohamed; Alghamdi, Badrah S; Perveen, Asma; Ashraf, Ghulam Md; Bahbah, Eshak I · Meta Analysis

RPEP-05588 · 2021

Substance P From Pain Neurons Triggers Allergic IgE Antibody Production

Nociceptor ablation/silencing substantially reduced allergic inflammation and IgE production in airway and skin models. Substance P released from nociceptors promoted B cell antibody class switching to IgE and antibody-secreting cell formation. First evidence of nociceptor role in adaptive humoral immunity.

Mathur, Shreya; Wang, Jo-Chiao; Seehus, Corey R; Poirier, Florence; Crosson, Theo; Hsieh, Yu-Chen; Doyle, Benjamin; Lee, Seungkyu; Woolf, Clifford J; Foster, Simmie L; Talbot, Sebastien · Animal Study