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

Dysregulated skeletal muscle myosin super-relaxation and energetics in male participants with type 2 diabetes mellitus.

2 型糖尿病男性患者骨骼肌肌球蛋白超松弛和能量代谢失调

Lewis Christopher T A, Moreno-Justicia Roger, Savoure Lola, Calvo Enrique, Bak Agata, Laitila Jenni, Seaborne Robert A E, Larsen Steen, Iwamoto Hiroyuki, Cefis Marina, Morais Jose A, Gouspillou Gilles, Alegre-Cebollada Jorge, Hawke Thomas J, Vazquez Jesús, Adrover Miquel, Marcangeli Vincent, Hammad Rami, Granet Jordan, Gaudreau Pierrette, Aubertin-Leheudre Mylène, Bélanger Marc, Robitaille Richard, Deshmukh Atul S, Ochala Julien

Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy

肌球蛋白抑制可部分挽救X连锁肌管性肌病中的肌纤维蛋白质组。

Gerlach Melhedegaard, Elise; Rostedt, Fanny; Gineste, Charlotte; Seaborne, Robert Ae; Dugdale, Hannah F; Belhac, Vladimir; Zanoteli, Edmar; Lawlor, Michael W; Mack, David L; Wallgren-Pettersson, Carina; Hessel, Anthony L; Jungbluth, Heinz; Laporte, Jocelyn; Saito, Yoshihiko; Nishino, Ichizo; Ochala, Julien; Laitila, Jenni

Pathogenic TNNT1 variants are associated with aberrant thin filament compliance and myofibre hyper-contractility.

致病性 TNNT1 变异与细丝顺应性异常和肌纤维过度收缩有关

Laitila Jenni, Lewis Christopher T A, Hessel Anthony L, Primiano Guido, Hernandez-Lain Aurelio, Fiorillo Chiara, Lawlor Michael W, Ottenheijm Coen A C, Jungbluth Heinz, Man Ka Fu, Fornili Arianna, Ochala Julien

Remodeling of skeletal muscle myosin metabolic states in hibernating mammals

冬眠哺乳动物骨骼肌肌球蛋白代谢状态的重塑

Lewis, Christopher T A; Melhedegaard, Elise G; Ognjanovic, Marija M; Olsen, Mathilde S; Laitila, Jenni; Seaborne, Robert A E; Gronset, Magnus; Zhang, Changxin; Iwamoto, Hiroyuki; Hessel, Anthony L; Kuehn, Michel N; Merino, Carla; Amigo, Nuria; Frobert, Ole; Giroud, Sylvain; Staples, James F; Goropashnaya, Anna V; Fedorov, Vadim B; Barnes, Brian; Toien, Oivind; Drew, Kelly; Sprenger, Ryan J; Ochala, Julien

Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb.

在具有 Neb 基因错义突变和无义突变的复合杂合子小鼠模型中,Nebulin 线粒体肌病得以重现

Laitila Jenni M, McNamara Elyshia L, Wingate Catherine D, Goullee Hayley, Ross Jacob A, Taylor Rhonda L, van der Pijl Robbert, Griffiths Lisa M, Harries Rachel, Ravenscroft Gianina, Clayton Joshua S, Sewry Caroline, Lawlor Michael W, Ottenheijm Coen A C, Bakker Anthony J, Ochala Julien, Laing Nigel G, Wallgren-Pettersson Carina, Pelin Katarina, Nowak Kristen J

Nemaline myopathies: a current view

线状肌病:当前观点

Sewry, Caroline A; Laitila, Jenni M; Wallgren-Pettersson, Carina

Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulation

两种通过选择性剪接产生的人类Nebulin亚型,分别包含外显子143或外显子144,及其发育调控

Lam, Le Thanh; Holt, Ian; Laitila, Jenni; Hanif, Mubashir; Pelin, Katarina; Wallgren-Pettersson, Carina; Sewry, Caroline A; Morris, Glenn E