| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Francesca De Lorenzo, Patrick Lüningschrör, Jinhan Nam, Liam Beckett, Federica Pilotto, Emilia Galli, Päivi Lindholm, Cora Rüdt von Collenberg, Simon Tii Mungwa, Sibylle Jablonka, Julia Kauder, Nadine Thau-Habermann, Susanne Petri, Dan Lindholm, Smita Saxena, Michael Sendtner, Mart Saarma, Merja H Voutilaine. CDNF rescues motor neurons in models of amyotrophic lateral sclerosis by targeting endoplasmic reticulum stress. Brain : a journal of neurology. 2023-03-17. PMID:36928391. |
amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects motor neurons (mns) in the spinal cord, brainstem, and motor cortex, leading to paralysis and eventually to death within 3 to 5 years of symptom onset. |
2023-03-17 |
2023-08-14 |
mouse |
| Hankui Liu, Liping Guan, Min Deng, Lars Bolund, Karsten Kristiansen, Jianguo Zhang, Yonglun Luo, Zhanchi Zhan. Integrative genetic and single cell RNA sequencing analysis provides new clues to the amyotrophic lateral sclerosis neurodegeneration. Frontiers in neuroscience. vol 17. 2023-03-06. PMID:36875658. |
the gradual loss of motor neurons (mns) in the brain and spinal cord is a hallmark of amyotrophic lateral sclerosis (als), but the mechanisms underlying neurodegeneration in als are still not fully understood. |
2023-03-06 |
2023-08-14 |
Not clear |
| b' Maru\\xc5\\xa1a Barbo, Metka Ravnik-Glava\\xc4\\x8. Extracellular Vesicles as Potential Biomarkers in Amyotrophic Lateral Sclerosis. Genes. vol 14. issue 2. 2023-02-25. PMID:36833252.' |
amyotrophic lateral sclerosis (als) is described as a fatal and rapidly progressive neurodegenerative disorder caused by the degeneration of upper motor neurons in the primary motor cortex and lower motor neurons of the brainstem and spinal cord. |
2023-02-25 |
2023-08-14 |
Not clear |
| Yousra El Ouaamari, Jasper Van den Bos, Barbara Willekens, Nathalie Cools, Inez Wen. Neurotrophic Factors as Regenerative Therapy for Neurodegenerative Diseases: Current Status, Challenges and Future Perspectives. International journal of molecular sciences. vol 24. issue 4. 2023-02-25. PMID:36835277. |
neurodegenerative diseases, including alzheimer's disease (ad), parkinson's disease (pd), huntington's disease (hd), multiple sclerosis (ms), spinal cord injury (sci), and amyotrophic lateral sclerosis (als), are characterized by acute or chronic progressive loss of one or several neuronal subtypes. |
2023-02-25 |
2023-08-14 |
Not clear |
| Yaning Zang, Xigui Lai, Conghui Li, Dongfang Ding, Ying Wang, Yi Zh. The Role of Gut Microbiota in Various Neurological and Psychiatric Disorders-An Evidence Mapping Based on Quantified Evidence. Mediators of inflammation. vol 2023. 2023-02-23. PMID:36816743. |
we searched for neurological diseases and psychiatric disorders, including alzheimer's disease (ad), attention deficit hyperactivity disorder (adhd), amyotrophic lateral sclerosis (als), autism spectrum disorder (asd), anorexia nervosa (an), bipolar disorder (bd), eating disorder (ed), generalized anxiety disorder (gad), major depressive disorder (mdd), multiple sclerosis (ms), obsessive compulsive disorder (ocd), parkinson's disease (pd), posttraumatic stress disorder (ptsd), spinal cord injury (sci), schizophrenia, and stroke. |
2023-02-23 |
2023-08-14 |
Not clear |
| Yoshitaka Tamaki, Jay P Ross, Paria Alipour, Charles-Étienne Castonguay, Boting Li, Helene Catoire, Daniel Rochefort, Makoto Urushitani, Ryosuke Takahashi, Joshua A Sonnen, Stefano Stifani, Patrick A Dion, Guy A Roulea. Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids. PLoS genetics. vol 19. issue 2. 2023-02-06. PMID:36745687. |
spinal cord extracts of amyotrophic lateral sclerosis spread tdp-43 pathology in cerebral organoids. |
2023-02-06 |
2023-08-14 |
human |
| Deepti Katiyar, Shipra Singhal, Priya Bansal, K Nagarajan, Parul Grove. Nutraceuticals and phytotherapeutics for holistic management of amyotrophic lateral sclerosis. 3 Biotech. vol 13. issue 2. 2023-01-30. PMID:36714551. |
amyotrophic lateral sclerosis" (als) is a progressive neuronal disorder that affects sensory neurons in the brain and spinal cord, causing loss of muscle control. |
2023-01-30 |
2023-08-14 |
Not clear |
| Ceri Houldsworth, Krishnan Padmakumari Sivaraman Nair, Ram Pankajam Harihara. Cognition and Quality of Life of People with Spinal Cord Injury. Progress in rehabilitation medicine. vol 8. 2023-01-27. PMID:36703799. |
the aim of this study was to assess the cognitive abilities of people with spinal cord injury (sci) using the edinburgh cognitive and behavior amyotrophic lateral sclerosis screen (ecas), a tool designed for testing cognition in individuals with limited hand motor function. |
2023-01-27 |
2023-08-14 |
Not clear |
| Elisa Duranti, Chiara Vill. Molecular Investigations of Protein Aggregation in the Pathogenesis of Amyotrophic Lateral Sclerosis. International journal of molecular sciences. vol 24. issue 1. 2023-01-08. PMID:36614144. |
amyotrophic lateral sclerosis (als) is a devastating progressive neurodegenerative disorder characterized by selective loss of lower and upper motor neurons (mns) in the brain and spinal cord, resulting in paralysis and eventually death due to respiratory insufficiency. |
2023-01-08 |
2023-08-14 |
Not clear |
| Anna Nigri, Eleonora Dalla Bella, Stefania Ferraro, Jean Paul Medina Carrion, Greta Demichelis, Enrica Bersano, Monica Consonni, Antje Bischof, Mario Stanziano, Sara Palermo, Giuseppe Lauria, Maria Grazia Bruzzone, Nico Papinutt. Cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. Annals of clinical and translational neurology. 2023-01-04. PMID:36599092. |
cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. |
2023-01-04 |
2023-08-14 |
Not clear |
| Anna Nigri, Eleonora Dalla Bella, Stefania Ferraro, Jean Paul Medina Carrion, Greta Demichelis, Enrica Bersano, Monica Consonni, Antje Bischof, Mario Stanziano, Sara Palermo, Giuseppe Lauria, Maria Grazia Bruzzone, Nico Papinutt. Cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. Annals of clinical and translational neurology. 2023-01-04. PMID:36599092. |
spinal cord degeneration is a hallmark of amyotrophic lateral sclerosis. |
2023-01-04 |
2023-08-14 |
Not clear |
| Anna Nigri, Eleonora Dalla Bella, Stefania Ferraro, Jean Paul Medina Carrion, Greta Demichelis, Enrica Bersano, Monica Consonni, Antje Bischof, Mario Stanziano, Sara Palermo, Giuseppe Lauria, Maria Grazia Bruzzone, Nico Papinutt. Cervical spinal cord atrophy in amyotrophic lateral sclerosis across disease stages. Annals of clinical and translational neurology. 2023-01-04. PMID:36599092. |
the assessment of gray matter and white matter cervical spinal cord atrophy across clinical stages defined using the king's staging system could advance the understanding of amyotrophic lateral sclerosis progression. |
2023-01-04 |
2023-08-14 |
Not clear |
| Prasamsa Pudasaini, Shashank Neupane, Bishal Dhakal, Abilasha Rana, Bishnu Deep Pathak, Sagun Dawad. Bulbar onset amyotrophic lateral sclerosis: A case report. Annals of medicine and surgery (2012). vol 84. 2022-12-30. PMID:36582871. |
amyotrophic lateral sclerosis is a rare progressive neurodegenerative disease that affects the brain and spinal cord nerve cells. |
2022-12-30 |
2023-08-14 |
Not clear |
| Long-Fang Tu, Tian-Ze Zhang, Yang-Fan Zhou, Qing-Qing Zhou, Hai-Biao Gong, Lei Liang, Lin-Na Hai, Nan-Xin You, Yang Su, Yong-Jun Chen, Xu-Kai Mo, Chang-Zheng Shi, Liang-Ping Luo, Wan-Yang Sun, Wen-Jun Duan, Hiroshi Kurihara, Yi-Fang Li, Rong-Rong H. GPX4 deficiency-dependent phospholipid peroxidation drives motor deficits of ALS. Journal of advanced research. vol 43. 2022-12-30. PMID:36585109. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease characterized by oxidative stress that triggers motor neurons loss in the brain and spinal cord. |
2022-12-30 |
2023-08-14 |
mouse |
| Fang Yang, Wen-Zhi Chen, Shi-Shi Jiang, Xiao-Hua Wang, Ren-Shi X. A candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein G. Neural regeneration research. vol 18. issue 7. 2022-12-26. PMID:36571358. |
a candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein g. heterogenous nuclear ribonucleoprotein g is down-regulated in the spinal cord of the tg(sod1*g93a)1gur (tg) amyotrophic lateral sclerosis mouse model. |
2022-12-26 |
2023-08-14 |
mouse |
| Fang Yang, Wen-Zhi Chen, Shi-Shi Jiang, Xiao-Hua Wang, Ren-Shi X. A candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein G. Neural regeneration research. vol 18. issue 7. 2022-12-26. PMID:36571358. |
we analyzed heterogenous nuclear ribonucleoprotein g distribution in spinal cord in the amyotrophic lateral sclerosis model at various time points and the expressions of apoptosis and proliferation-related proteins. |
2022-12-26 |
2023-08-14 |
mouse |
| Fang Yang, Wen-Zhi Chen, Shi-Shi Jiang, Xiao-Hua Wang, Ren-Shi X. A candidate protective factor in amyotrophic lateral sclerosis: heterogenous nuclear ribonucleoprotein G. Neural regeneration research. vol 18. issue 7. 2022-12-26. PMID:36571358. |
our study suggests that abnormal distribution and expression of heterogenous nuclear ribonucleoprotein g might play a protective effect in amyotrophic lateral sclerosis development via preventing neuronal death by reducing abnormal tar dna binding protein 43 generation in the spinal cord. |
2022-12-26 |
2023-08-14 |
mouse |
| Winanto Ng, Shi-Yan N. Remodeling of astrocyte secretome in amyotrophic lateral sclerosis: uncovering novel targets to combat astrocyte-mediated toxicity. Translational neurodegeneration. vol 11. issue 1. 2022-12-25. PMID:36567359. |
amyotrophic lateral sclerosis (als) is an adult-onset paralytic disease characterized by progressive degeneration of upper and lower motor neurons in the motor cortex, brainstem and spinal cord. |
2022-12-25 |
2023-08-14 |
Not clear |
| Yu Hashimoto, Ryo Yamasaki, Senri Ko, Eriko Matsuo, Yuko Kobayakawa, Katsuhisa Masaki, Dai Matsuse, Noriko Isob. Connexin 30 Deficiency Ameliorates Disease Progression at the Early Phase in a Mouse Model of Amyotrophic Lateral Sclerosis by Suppressing Glial Inflammation. International journal of molecular sciences. vol 23. issue 24. 2022-12-23. PMID:36555685. |
cx30 is upregulated on activated astroglia in central nervous system inflammatory lesions, including spinal cord lesions in mutant superoxide dismutase 1 (msod1) transgenic amyotrophic lateral sclerosis (als) model mice. |
2022-12-23 |
2023-08-14 |
mouse |
| Jennifer L Sippel, Jennifer E Daly, Linda Poggensee, Kim D Ristau, Adam C Eberhart, Katharine Tam, Charlesnika T Evans, Betsy Lancaster, I Manosha Wickremasinghe, Stephen P Burns, Barry Goldstein, Bridget M Smit. Modernization of a Large Spinal Cord Injuries and Disorders Registry: The Veterans Administration Experience. Archives of rehabilitation research and clinical translation. vol 4. issue 4. 2022-12-22. PMID:36545529. |
the vsr also comprises one of the only registries for individuals with non-traumatic sci/ds and holds potential to advance research and treatment for multiple sclerosis (ms), amyotrophic lateral sclerosis (als), and other motor neuron disorders with spinal cord involvement. |
2022-12-22 |
2023-08-14 |
Not clear |