Results 211 to 220 of about 1,078,640 (312)

MOESM1 of Plasmodium falciparum parasite population structure and gene flow associated to anti-malarial drugs resistance in Cambodia

, 2016
Ankit Dwivedi, Nimol Khim, Christelle Reynès, Patrice Ravel, Laurence Ma, Magali Tichit, Christiane Bourchier, Saorin Kim, Dany Dourng, Chanra Khean, Pheaktra Chim, Siv Sovannaroth, Roger Frutos, Dysoley Lek, Odile Mercereau‐Puijalon, FrĂŠdĂŠric Ariey, Didier Ménard, Emmanuel Cornillot   +17 more
openalex   +1 more source

Changes in Immune‐Inflammation Status and Acute Ischemic Stroke Prognosis in Prospective Cohort

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Inflammation is a critical risk factor for poor outcomes in cerebral infarction. Prior studies focused primarily on baseline inflammation status, neglecting dynamic longitudinal changes. We try to investigate the association between immune‐inflammation status alterations and stroke prognosis, and evaluated three systemic biomarkers'
Songfang Chen, Wenting Huang, Yitian Liu, Xuan Chen, Buyu Ke, Qian Shen, Hanyu Cai, Jing Sun, Yan Li, Yungang Cao, Beilei Hu, Keyang Chen   +11 more
wiley   +1 more source

3D Genome Constrains Breakpoints of Inversions That Can Act as Barriers to Gene Flow in the Stickleback. [PDF]

Mol Ecol
Yamasaki YY, Toyoda A, Kadota M, Kuraku S, Kitano J.   +4 more
europepmc   +1 more source

GENE FLOW IN NATURAL POPULATIONS OF CARICA PAPAYA IN THE FRAGMENTED LANDSCAPES OF COSTA RICA AND NICARAGUA

, 2016
Kel R Arlinghaus
openalex   +1 more source

Chronological and Spatial Distribution of Skeletal Muscle Fat Replacement in FHL1‐Related Myopathies

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives Variants in the FHL1 gene cause FHL1‐related myopathies (FHL1‐RMs), a group of neuromuscular disorders with diverse clinical presentations. This study aimed to comprehensively characterize the spatial and temporal patterns of skeletal muscle fat replacement throughout the whole body in FHL1‐RMs, to examine disease progression over ...
Rui Shimazaki, Satoru Noguchi, Hotake Takizawa, Yasushi Oya, Yuji Takahashi, Hirofumi Komaki, Hajime Arahata, Shinichiro Hayashi, Ichizo Nishino   +8 more
wiley   +1 more source

Evidence of high genetic differentiation driven by limited gene flow in a lower canopy African tropical rainforest tree species, Coula edulis Baill. (Coulaceae). [PDF]

BMC Ecol Evol
Kamdem NG, Sonké B, Sergeant S, Stevart T, Deblauwe V, Hardy OJ.   +5 more
europepmc   +1 more source

The T-786C and Glu298Asp polymorphisms of the endothelial nitric oxide gene affect the forearm blood flow responses of Caucasian hypertensive patients

, 2003
Gian Paolo Rossi, Stefano Taddei, Agostino Virdis, Martina Cavallin, Lorenzo Ghiadoni, Stefania Favilla, Daniele Versari, Isabella Sudano, Achille C. Pessina, Antonio Salvetti   +9 more
openalex   +2 more sources

Olink Proteomics Analysis Reveals Heterogeneous Responses to FcRn Blockade in Anti‐AChR Antibody‐Positive Myasthenia Gravis: FGF‐19 as a Novel Biomarker

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective This study aimed to systematically observe the clinical manifestations, immune cell subsets, and dynamic changes in serological indicators in patients with myasthenia gravis (MG) before and after efgartigimod (EFG) treatment. Methods We analyzed the baseline data, laboratory parameters, and lymphocyte subset proportions in MG ...
Tiancheng Luo, Deyou Peng, Zhouao Zhang, Mingjin Yang, Xinyan Guo, Tianyu Ma, Xiaoyu Huang, Mingming Xu, Linlin Fu, Yong Zhang   +9 more
wiley   +1 more source

Pervasive gene flow despite strong and varied reproductive barriers in swordtails. [PDF]

Nat Ecol Evol
Aguillon SM, Haase Cox SK, Langdon QK, Gunn TR, Baczenas JJ, Banerjee SM, Donny AE, Moran BM, Fascinetto-Zago P, Gutiérrez-Rodríguez C, Ríos-Cárdenas O, Morris MR, Powell DL, Schumer M.   +13 more
europepmc   +1 more source

Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian, Peter Auguste, Amy Grove, Anna Brown, Janette Parr, Mubarak Patel, Furqan Butt, Jeremiah Donoghue, Mehdi Yousefi, Jo Parsons   +9 more
wiley   +1 more source