Nennesmo相关文献与解析，生知库 | 链接生命科学的每一步

Gonzalez-Chapa, Jorge A; Horuluoglu, Begum; Notarnicola, Antonella; Rathee, Arpit; Kaur, Noor; Stultz, Ryan D; Christopher-Stine, Lisa; Albayda, Jemima; Nennesmo, Inger; Lundberg, Ingrid E; Lood, Christian

中性粒细胞

炎症/感染

细胞生物学

Acquired Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline in Sweden-A Nationwide Population-Based Study

瑞典一项基于全国人口的研究：舍曲林相关获得性多酰基辅酶A脱氢酶缺乏症

期刊:European Journal of Neurology

影响因子:3.9

doi:10.1111/ene.70555

Sunebo, Sofie; Nilsson, Emil; Engvall, Martin; Hedberg-Oldfors, Carola; Shen, Yan; Nennesmo, Inger; Danielsson, Olof; Oldfors, Anders; Appelqvist, Hanna; Lindgren, Ulrika

发表日期：2026

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The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

ZFHX3 GGC 重复序列扩增是 4 型脊髓小脑性共济失调的根本原因，它具有共同的祖先。

期刊:Movement Disorders

影响因子:7.6

doi:10.1002/mds.30077

Chen, Zhongbo; Alvarez Jerez, Pilar; Anderson, Claire; Paucar, Martin; Lee, Jasmaine; Nilsson, Daniel; Macpherson, Hannah; Scardamaglia, Annarita; Montgomery, Kylie; Hardy, John; Singleton, Andrew B; Tucci, Arianna; Mathews, Katherine D; Fu, Ying-Hui; Engvall, Martin; Laffita-Mesa, José; Nennesmo, Inger; Wedell, Anna; Ptáček, Louis J; Blauwendraat, Cornelis; Gustavsson, Emil K; Svenningsson, Per; Ryten, Mina; Houlden, Henry

神经科学

发表日期：2025

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Phenotypic variability in early-onset dementia segregating with a novel APP (p.I718M) variant

早发性痴呆的表型变异与一种新的APP（p.I718M）变异相关

期刊:Alzheimers Research & Therapy

影响因子:7.6

doi:10.1186/s13195-025-01890-9

Johansson, Charlotte; Rodriguez-Vieitez, Elena; Bluma, Marina; Nennesmo, Inger; Thonberg, Håkan; Ullgren, Abbe; Jelic, Vesna; Zetterberg, Henrik; Blennow, Kaj; Nordberg, Agneta; Graff, Caroline

APP

发表日期：2025

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Author Correction: A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

作者更正：一种新生、嵌合且复杂的21号染色体重排导致APP三倍体和家族性常染色体显性遗传早发性阿尔茨海默病。

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-025-94140-9

Ehn, Emma; Eisfeldt, Jesper; Laffita-Mesa, Jose M; Thonberg, Håkan; Schoumans, Jacqueline; Portaankorva, Anne M; Viitanen, Matti; Lindstrand, Anna; Nennesmo, Inger; Graff, Caroline

A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

一种新生、嵌合且复杂的21号染色体重排导致APP三倍体和家族性常染色体显性遗传早发性阿尔茨海默病。

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-025-86645-0

Ehn, Emma; Eisfeldt, Jesper; Laffita-Mesa, Jose M; Thonberg, Håkan; Schoumans, Jacqueline; Portaankorva, Anne M; Viitanen, Matti; Lindstrand, Anna; Nennesmo, Inger; Graff, Caroline

Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies.

越南特发性炎症性肌病患者队列的免疫特征分析

期刊:Muscle & Nerve

影响因子:3.1

doi:10.1002/mus.28455

Luo Yue-Bei, Nakazawa Maho, Minh Nham Pham Thi, Heinon LÃ©o, Nennesmo Inger, RÃ¶nnelid Johan, Lundberg Ingrid E, Phuong Thuy Nguyen Thi, Horuluoglu Begum

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues

在成年哺乳动物组织中，PARKIN 不是维持 OXPHOS 功能所必需的

期刊:Npj Parkinsons Disease

影响因子:6.7

doi:10.1038/s41531-024-00707-0

Roberta Filograna, Jule Gerlach, Hae-Na Choi, Giovanni Rigoni, Michela Barbaro, Mikael Oscarson, Seungmin Lee, Katarina Tiklova, Markus Ringnér, Camilla Koolmeister, Rolf Wibom, Sara Riggare, Inger Nennesmo, Thomas Perlmann, Anna Wredenberg, Anna Wedell, Elisa Motori, Per Svenningsson, Nils-Göran La

Single-cell profiling of muscle-infiltrating T cells in idiopathic inflammatory myopathies

特发性炎症性肌病中肌肉浸润 T 细胞的单细胞分析

期刊:EMBO Molecular Medicine

影响因子:9

doi:10.15252/emmm.202217240

Alexandra Argyriou #, Begum Horuluoglu #, Angeles Shunashy Galindo-Feria #, Juan Sebastian Diaz-Boada, Merel Sijbranda, Antonella Notarnicola, Lara Dani, Annika van Vollenhoven, Daniel Ramsköld, Inger Nennesmo, Maryam Dastmalchi, Ingrid E Lundberg, Lina-Marcela Diaz-Gallo #, Karine Chemin #

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3

与 XPNPEP3 基因中一种新的纯合变异相关的伴有听力丧失和肾痨的共济失调综合征

期刊:Neurology-Genetics

影响因子:3.7

doi:10.1212/NXG.0000000000200100

Ben-Shabat, Ilan; Kvarnung, Malin; Sperker, Wolfgang; Bruhn, Helene; Wredenberg, Anna; Wibom, Rolf; Nennesmo, Inger; Engvall, Martin; Paucar, Martin

发表日期：2023

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N-formyl methionine peptide-driven neutrophil activation in idiopathic inflammatory myopathies

N-甲酰甲硫氨酸肽驱动的中性粒细胞活化在特发性炎症性肌病中的作用

Acquired Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline in Sweden-A Nationwide Population-Based Study

瑞典一项基于全国人口的研究：舍曲林相关获得性多酰基辅酶A脱氢酶缺乏症

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

ZFHX3 GGC 重复序列扩增是 4 型脊髓小脑性共济失调的根本原因，它具有共同的祖先。

Phenotypic variability in early-onset dementia segregating with a novel APP (p.I718M) variant

早发性痴呆的表型变异与一种新的APP（p.I718M）变异相关

Author Correction: A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

作者更正：一种新生、嵌合且复杂的21号染色体重排导致APP三倍体和家族性常染色体显性遗传早发性阿尔茨海默病。

A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

一种新生、嵌合且复杂的21号染色体重排导致APP三倍体和家族性常染色体显性遗传早发性阿尔茨海默病。

Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies.

越南特发性炎症性肌病患者队列的免疫特征分析

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues

在成年哺乳动物组织中，PARKIN 不是维持 OXPHOS 功能所必需的

Single-cell profiling of muscle-infiltrating T cells in idiopathic inflammatory myopathies

特发性炎症性肌病中肌肉浸润 T 细胞的单细胞分析

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3

与 XPNPEP3 基因中一种新的纯合变异相关的伴有听力丧失和肾痨的共济失调综合征