日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Brain-Region-Specific Differences in Protein Citrullination/Deimination in a Pre-Motor Parkinson's Disease Rat Model

运动前帕金森病大鼠模型中蛋白质瓜氨酸化/脱氨基化的脑区特异性差异

Audrey Mercer, Marco Sancandi, Amy Maclatchy, Sigrun Lange

Effects of a probiotic suspension Symprove™ on a rat early-stage Parkinson's disease model

益生菌悬浮液 Symprove™ 对大鼠早期帕金森病模型的影响

Marco Sancandi, Carmen De Caro, Neringa Cypaite, Nadia Marascio, Carmen Avagliano, Carmela De Marco, Emilio Russo, Andrew Constanti, Audrey Mercer

Protein Deimination Signatures in Plasma and Plasma-EVs and Protein Deimination in the Brain Vasculature in a Rat Model of Pre-Motor Parkinson's Disease

运动前帕金森病大鼠模型中血浆和血浆电动汽车中的蛋白质脱亚胺特征以及脑血管中的蛋白质脱亚胺

Marco Sancandi, Pinar Uysal-Onganer, Igor Kraev, Audrey Mercer, Sigrun Lange

Structural Changes Observed in the Piriform Cortex in a Rat Model of Pre-motor Parkinson's Disease

在运动前帕金森病大鼠模型中观察到的梨状皮质结构变化

Marco Sancandi, Emma Victoria Schul, Georgia Economides, Andrew Constanti, Audrey Mercer

Dopamine neuronal loss contributes to memory and reward dysfunction in a model of Alzheimer's disease

在阿尔茨海默病模型中,多巴胺神经元丢失会导致记忆和奖赏功能障碍。

Annalisa Nobili ,Emanuele Claudio Latagliata ,Maria Teresa Viscomi ,Virve Cavallucci ,Debora Cutuli ,Giacomo Giacovazzo ,Paraskevi Krashia ,Francesca Romana Rizzo ,Ramona Marino ,Mauro Federici ,Paola De Bartolo ,Daniela Aversa ,Maria Concetta Dell'Acqua ,Alberto Cordella ,Marco Sancandi ,Flavio Keller ,Laura Petrosini ,Stefano Puglisi-Allegra ,Nicola Biagio Mercuri ,Roberto Coccurello ,Nicola Berretta ,Marcello D'Amelio

Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease

RET原癌基因5'区域的单核苷酸多态性等位基因定义了先天性巨结肠症的风险单倍型。

Sancandi, M; Griseri, P; Pesce, B; Patrone, G; Puppo, F; Lerone, M; Martucciello, G; Romeo, G; Ravazzolo, R; Devoto, M; Ceccherini, I

A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease

RET原癌基因的一种罕见单倍型是先天性巨结肠症的风险修饰等位基因。

Griseri, Paola; Pesce, Barbara; Patrone, Giovanna; Osinga, Jan; Puppo, Francesca; Sancandi, Monica; Hofstra, Robert; Romeo, Giovanni; Ravazzolo, Roberto; Devoto, Marcella; Ceccherini, Isabella

A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?

Waardenburg-Hirschsprung 病中的内皮素 3 杂合突变:EDN3/EDNRB 基因突变对神经嵴病表型是否存在剂量效应?

Pingault, V; Bondurand, N; Lemort, N; Sancandi, M; Ceccherini, I; Hugot, J P; Jouk, P S; Goossens, M

Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

评估 HOX11L1 基因作为先天性肠道神经支配障碍候选基因的价值

Costa, M; Fava, M; Seri, M; Cusano, R; Sancandi, M; Forabosco, P; Lerone, M; Martucciello, G; Romeo, G; Ceccherini, I