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Myostatin promotes tenogenic differentiation of C2C12 myoblast cells through Smad3.

FEBS open bio

Uemura K, Hayashi M, Itsubo T, Oishi A, Iwakawa H, Komatsu M, Uchiyama S, Kato H.
PMID: 28396837
FEBS Open Bio. 2017 Feb 20;7(4):522-532. doi: 10.1002/2211-5463.12200. eCollection 2017 Apr.

Myostatin, a member of the transforming growth factor-β (TGF-β) superfamily, is expressed in developing and adult skeletal muscle and negatively regulates skeletal muscle growth. Recently, myostatin has been found to be expressed in tendons and increases tendon fibroblast proliferation...

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Uemura K, Hayashi M, Itsubo T, et al. Myostatin promotes tenogenic differentiation of C2C12 myoblast cells through Smad3. FEBS Open Bio. 2017;7(4):522-532doi: 10.1002/2211-5463.12200.
Uemura, K., Hayashi, M., Itsubo, T., Oishi, A., Iwakawa, H., Komatsu, M., Uchiyama, S., & Kato, H. (2017). Myostatin promotes tenogenic differentiation of C2C12 myoblast cells through Smad3. FEBS open bio, 7(4), 522-532. https://doi.org/10.1002/2211-5463.12200
Uemura, Kazutaka, et al. "Myostatin promotes tenogenic differentiation of C2C12 myoblast cells through Smad3." FEBS open bio vol. 7,4 (2017): 522-532. doi: https://doi.org/10.1002/2211-5463.12200
Uemura K, Hayashi M, Itsubo T, Oishi A, Iwakawa H, Komatsu M, Uchiyama S, Kato H. Myostatin promotes tenogenic differentiation of C2C12 myoblast cells through Smad3. FEBS Open Bio. 2017 Feb 20;7(4):522-532. doi: 10.1002/2211-5463.12200. eCollection 2017 Apr. PMID: 28396837; PMCID: PMC5377394.
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Technical feasibility of line-assisted complete closure technique for large mucosal defects after colorectal endoscopic submucosal dissection.

Endoscopy international open

Kato M, Takeuchi Y, Yamasaki Y, Arao M, Suzuki S, Iwatsubo T, Hamada K, Tonai Y, Shichijo S, Matsuura N, Nakahira H, Kanesaka T, Akasaka T, Hanaoka N, Higashino K, Uedo N, Ishihara R, Iishi H.
PMID: 28337479
Endosc Int Open. 2017 Jan;5(1):E11-E16. doi: 10.1055/s-0042-121002.

No abstract available.

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Kato M, Takeuchi Y, Yamasaki Y, et al. Technical feasibility of line-assisted complete closure technique for large mucosal defects after colorectal endoscopic submucosal dissection. Endosc Int Open. 2017;5(1):E11-E16doi: 10.1055/s-0042-121002.
Kato, M., Takeuchi, Y., Yamasaki, Y., Arao, M., Suzuki, S., Iwatsubo, T., Hamada, K., Tonai, Y., Shichijo, S., Matsuura, N., Nakahira, H., Kanesaka, T., Akasaka, T., Hanaoka, N., Higashino, K., Uedo, N., Ishihara, R., & Iishi, H. (2017). Technical feasibility of line-assisted complete closure technique for large mucosal defects after colorectal endoscopic submucosal dissection. Endoscopy international open, 5(1), E11-E16. https://doi.org/10.1055/s-0042-121002
Kato, Minoru, et al. "Technical feasibility of line-assisted complete closure technique for large mucosal defects after colorectal endoscopic submucosal dissection." Endoscopy international open vol. 5,1 (2017): E11-E16. doi: https://doi.org/10.1055/s-0042-121002
Kato M, Takeuchi Y, Yamasaki Y, Arao M, Suzuki S, Iwatsubo T, Hamada K, Tonai Y, Shichijo S, Matsuura N, Nakahira H, Kanesaka T, Akasaka T, Hanaoka N, Higashino K, Uedo N, Ishihara R, Iishi H. Technical feasibility of line-assisted complete closure technique for large mucosal defects after colorectal endoscopic submucosal dissection. Endosc Int Open. 2017 Jan;5(1):E11-E16. doi: 10.1055/s-0042-121002. PMID: 28337479; PMCID: PMC5361877.
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Imago Mundi, Imago AD, Imago ADNI.

Alzheimer's research & therapy

Villemagne VL, Kim SY, Rowe CC, Iwatsubo T.
PMID: 25478022
Alzheimers Res Ther. 2014 Aug 29;6(5):62. doi: 10.1186/s13195-014-0062-5. eCollection 2014.

Since the launch in 2003 of the Alzheimer's Disease Neuroimaging Initiative (ADNI) in the USA, ever growing, similarly oriented consortia have been organized and assembled around the world. The various accomplishments of ADNI have contributed substantially to a better...

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Villemagne VL, Kim SY, Rowe CC, et al. Imago Mundi, Imago AD, Imago ADNI. Alzheimers Res Ther. 2014;6(5):62doi: 10.1186/s13195-014-0062-5.
Villemagne, V. L., Kim, S. Y., Rowe, C. C., & Iwatsubo, T. (2014). Imago Mundi, Imago AD, Imago ADNI. Alzheimer's research & therapy, 6(5), 62. https://doi.org/10.1186/s13195-014-0062-5
Villemagne, Victor L, et al. "Imago Mundi, Imago AD, Imago ADNI." Alzheimer's research & therapy vol. 6,5 (2014): 62. doi: https://doi.org/10.1186/s13195-014-0062-5
Villemagne VL, Kim SY, Rowe CC, Iwatsubo T. Imago Mundi, Imago AD, Imago ADNI. Alzheimers Res Ther. 2014 Aug 29;6(5):62. doi: 10.1186/s13195-014-0062-5. eCollection 2014. PMID: 25478022; PMCID: PMC4255533.
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Presenilin-dependent intramembrane cleavage of ephrin-B1.

Molecular neurodegeneration

Tomita T, Tanaka S, Morohashi Y, Iwatsubo T.
PMID: 16930449
Mol Neurodegener. 2006 Jun 12;1:2. doi: 10.1186/1750-1326-1-2.

BACKGROUND: Presenilin-dependent gamma-secretase cleavage of several transmembrane proteins, including amyloid-beta precursor protein and Notch, mediates the intramembrane proteolysis to liberate their intracellular domains that are involved in cellular signaling. Considering gamma-secretase inhibitors as therapeutics for Alzheimer's disease, understanding the...

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Tomita T, Tanaka S, Morohashi Y, et al. Presenilin-dependent intramembrane cleavage of ephrin-B1. Mol Neurodegener. 2006;1:2doi: 10.1186/1750-1326-1-2.
Tomita, T., Tanaka, S., Morohashi, Y., & Iwatsubo, T. (2006). Presenilin-dependent intramembrane cleavage of ephrin-B1. Molecular neurodegeneration, 12. https://doi.org/10.1186/1750-1326-1-2
Tomita, Taisuke, et al. "Presenilin-dependent intramembrane cleavage of ephrin-B1." Molecular neurodegeneration vol. 1 (2006): 2. doi: https://doi.org/10.1186/1750-1326-1-2
Tomita T, Tanaka S, Morohashi Y, Iwatsubo T. Presenilin-dependent intramembrane cleavage of ephrin-B1. Mol Neurodegener. 2006 Jun 12;1:2. doi: 10.1186/1750-1326-1-2. PMID: 16930449; PMCID: PMC1513130.
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Effects of sex, educational background, and chronic kidney disease grading on longitudinal cognitive and functional decline in patients in the Japanese Alzheimer's Disease Neuroimaging Initiative study.

Alzheimer's & dementia (New York, N. Y.)

Iwata A, Iwatsubo T, Ihara R, Suzuki K, Matsuyama Y, Tomita N, Arai H, Ishii K, Senda M, Ito K, Ikeuchi T, Kuwano R, Matsuda H.
PMID: 30662934
Alzheimers Dement (N Y). 2018 Jul 12;4:765-774. doi: 10.1016/j.trci.2018.06.008. eCollection 2018.

INTRODUCTION: The objective of this study was to determine whether sex or education level affects the longitudinal rate of cognitive decline in Japanese patients in the Alzheimer's disease Neuroimaging Initiative study with defined mild cognitive impairment (MCI).METHODS: We accessed...

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Iwata A, Iwatsubo T, Ihara R, et al. Effects of sex, educational background, and chronic kidney disease grading on longitudinal cognitive and functional decline in patients in the Japanese Alzheimer's Disease Neuroimaging Initiative study. Alzheimers Dement (N Y). 2018;4:765-774doi: 10.1016/j.trci.2018.06.008.
Iwata, A., Iwatsubo, T., Ihara, R., Suzuki, K., Matsuyama, Y., Tomita, N., Arai, H., Ishii, K., Senda, M., Ito, K., Ikeuchi, T., Kuwano, R., Matsuda, H. (2018). Effects of sex, educational background, and chronic kidney disease grading on longitudinal cognitive and functional decline in patients in the Japanese Alzheimer's Disease Neuroimaging Initiative study. Alzheimer's & dementia (New York, N. Y.), 4765-774. https://doi.org/10.1016/j.trci.2018.06.008
Iwata, Atsushi, et al. "Effects of sex, educational background, and chronic kidney disease grading on longitudinal cognitive and functional decline in patients in the Japanese Alzheimer's Disease Neuroimaging Initiative study." Alzheimer's & dementia (New York, N. Y.) vol. 4 (2018): 765-774. doi: https://doi.org/10.1016/j.trci.2018.06.008
Iwata A, Iwatsubo T, Ihara R, Suzuki K, Matsuyama Y, Tomita N, Arai H, Ishii K, Senda M, Ito K, Ikeuchi T, Kuwano R, Matsuda H. Effects of sex, educational background, and chronic kidney disease grading on longitudinal cognitive and functional decline in patients in the Japanese Alzheimer's Disease Neuroimaging Initiative study. Alzheimers Dement (N Y). 2018 Jul 12;4:765-774. doi: 10.1016/j.trci.2018.06.008. eCollection 2018. PMID: 30662934; PMCID: PMC6324255.
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Endoscopic appearance of esophageal xanthoma.

Endoscopy international open

Hamada K, Uedo N, Kubo C, Tomita Y, Ishihara R, Yamasaki Y, Omori M, Arao M, Suzuki S, Iwatsubo T, Kato M, Tonai Y, Shichijo S, Matsuura N, Nakahira H, Kanesaka T, Yamamoto S, Akasaka T, Hanaoka N, Takeuchi Y, Higashino K, Okada H, Iishi H.
PMID: 31579702
Endosc Int Open. 2019 Oct;7(10):E1214-E1220. doi: 10.1055/a-0966-8544. Epub 2019 Oct 01.

No abstract available.

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Hamada K, Uedo N, Kubo C, et al. Endoscopic appearance of esophageal xanthoma. Endosc Int Open. 2019;7(10):E1214-E1220doi: 10.1055/a-0966-8544.
Hamada, K., Uedo, N., Kubo, C., Tomita, Y., Ishihara, R., Yamasaki, Y., Omori, M., Arao, M., Suzuki, S., Iwatsubo, T., Kato, M., Tonai, Y., Shichijo, S., Matsuura, N., Nakahira, H., Kanesaka, T., Yamamoto, S., Akasaka, T., Hanaoka, N., Takeuchi, Y., Higashino, K., Okada, H., & Iishi, H. (2019). Endoscopic appearance of esophageal xanthoma. Endoscopy international open, 7(10), E1214-E1220. https://doi.org/10.1055/a-0966-8544
Hamada, Kenta, et al. "Endoscopic appearance of esophageal xanthoma." Endoscopy international open vol. 7,10 (2019): E1214-E1220. doi: https://doi.org/10.1055/a-0966-8544
Hamada K, Uedo N, Kubo C, Tomita Y, Ishihara R, Yamasaki Y, Omori M, Arao M, Suzuki S, Iwatsubo T, Kato M, Tonai Y, Shichijo S, Matsuura N, Nakahira H, Kanesaka T, Yamamoto S, Akasaka T, Hanaoka N, Takeuchi Y, Higashino K, Okada H, Iishi H. Endoscopic appearance of esophageal xanthoma. Endosc Int Open. 2019 Oct;7(10):E1214-E1220. doi: 10.1055/a-0966-8544. Epub 2019 Oct 01. PMID: 31579702; PMCID: PMC6773585.
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Impact of electrosurgical unit mode on post esophageal endoscopic submucosal dissection stricture in an in vivo porcine model.

Endoscopy international open

Tonai Y, Ishihara R, Yamasaki Y, Arao M, Iwatsubo T, Kato M, Suzuki S, Hamada K, Shichijo S, Matsuura N, Kanesaka T, Nakahira H, Yamamoto S, Akasaka T, Hanaoka N, Takeuchi Y, Higashino K, Uedo N, Tomita Y, Iishi H.
PMID: 29527561
Endosc Int Open. 2018 Mar;6(3):E376-E381. doi: 10.1055/s-0043-122883. Epub 2018 Mar 07.

BACKGROUND AND AIM:  Strictures are a major complication of esophageal endoscopic submucosal dissection (ESD) for superficial esophageal carcinoma. Post ESD, stricture develops during the process of scar formation, which is related to inflammation caused by ESD. We planned a...

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Tonai Y, Ishihara R, Yamasaki Y, et al. Impact of electrosurgical unit mode on post esophageal endoscopic submucosal dissection stricture in an in vivo porcine model. Endosc Int Open. 2018;6(3):E376-E381doi: 10.1055/s-0043-122883.
Tonai, Y., Ishihara, R., Yamasaki, Y., Arao, M., Iwatsubo, T., Kato, M., Suzuki, S., Hamada, K., Shichijo, S., Matsuura, N., Kanesaka, T., Nakahira, H., Yamamoto, S., Akasaka, T., Hanaoka, N., Takeuchi, Y., Higashino, K., Uedo, N., Tomita, Y., & Iishi, H. (2018). Impact of electrosurgical unit mode on post esophageal endoscopic submucosal dissection stricture in an in vivo porcine model. Endoscopy international open, 6(3), E376-E381. https://doi.org/10.1055/s-0043-122883
Tonai, Yusuke, et al. "Impact of electrosurgical unit mode on post esophageal endoscopic submucosal dissection stricture in an in vivo porcine model." Endoscopy international open vol. 6,3 (2018): E376-E381. doi: https://doi.org/10.1055/s-0043-122883
Tonai Y, Ishihara R, Yamasaki Y, Arao M, Iwatsubo T, Kato M, Suzuki S, Hamada K, Shichijo S, Matsuura N, Kanesaka T, Nakahira H, Yamamoto S, Akasaka T, Hanaoka N, Takeuchi Y, Higashino K, Uedo N, Tomita Y, Iishi H. Impact of electrosurgical unit mode on post esophageal endoscopic submucosal dissection stricture in an in vivo porcine model. Endosc Int Open. 2018 Mar;6(3):E376-E381. doi: 10.1055/s-0043-122883. Epub 2018 Mar 07. PMID: 29527561; PMCID: PMC5842068.
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Relations Among Reinvestment, Self-Regulation, and Perception of Choking Under Pressure.

Journal of human kinetics

Iwatsuki T, Raalte JLV, Brewer BW, Petitpas A, Takahashi M.
PMID: 30687439
J Hum Kinet. 2018 Dec 31;65:281-290. doi: 10.2478/hukin-2018-0042. eCollection 2018 Dec.

The purpose of this study was to examine relations among reinvestment, self-regulation, and perception of choking under pressure in skilled tennis players. Participants were 160 collegiate players from the NCAA Division I in the U.S. and the 1st League...

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Iwatsuki T, Raalte JLV, Brewer BW, et al. Relations Among Reinvestment, Self-Regulation, and Perception of Choking Under Pressure. J Hum Kinet. 2018;65:281-290doi: 10.2478/hukin-2018-0042.
Iwatsuki, T., Raalte, J. L. V., Brewer, B. W., Petitpas, A., & Takahashi, M. (2018). Relations Among Reinvestment, Self-Regulation, and Perception of Choking Under Pressure. Journal of human kinetics, 65281-290. https://doi.org/10.2478/hukin-2018-0042
Iwatsuki, Takehiro, et al. "Relations Among Reinvestment, Self-Regulation, and Perception of Choking Under Pressure." Journal of human kinetics vol. 65 (2018): 281-290. doi: https://doi.org/10.2478/hukin-2018-0042
Iwatsuki T, Raalte JLV, Brewer BW, Petitpas A, Takahashi M. Relations Among Reinvestment, Self-Regulation, and Perception of Choking Under Pressure. J Hum Kinet. 2018 Dec 31;65:281-290. doi: 10.2478/hukin-2018-0042. eCollection 2018 Dec. PMID: 30687439; PMCID: PMC6341961.
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ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity.

Neurobiology of disease

An H, Litscher G, Watanabe N, Wei W, Hashimoto T, Iwatsubo T, Buchman VL, Shelkovnikova TA.
PMID: 34915152
Neurobiol Dis. 2022 Jan;162:105585. doi: 10.1016/j.nbd.2021.105585. Epub 2021 Dec 14.

Formation of cytoplasmic RNA-protein structures called stress granules (SGs) is a highly conserved cellular response to stress. Abnormal metabolism of SGs may contribute to the pathogenesis of (neuro)degenerative diseases such as amyotrophic lateral sclerosis (ALS). Many SG proteins are...

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An H, Litscher G, Watanabe N, et al. ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity. Neurobiol Dis. 2021;162:105585doi: 10.1016/j.nbd.2021.105585.
An, H., Litscher, G., Watanabe, N., Wei, W., Hashimoto, T., Iwatsubo, T., Buchman, V. L., & Shelkovnikova, T. A. (2022). ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity. Neurobiology of disease, 162105585. https://doi.org/10.1016/j.nbd.2021.105585
An, Haiyan, et al. "ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity." Neurobiology of disease vol. 162 (2022): 105585. doi: https://doi.org/10.1016/j.nbd.2021.105585
An H, Litscher G, Watanabe N, Wei W, Hashimoto T, Iwatsubo T, Buchman VL, Shelkovnikova TA. ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity. Neurobiol Dis. 2022 Jan;162:105585. doi: 10.1016/j.nbd.2021.105585. Epub 2021 Dec 14. PMID: 34915152.
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Underdiagnosis of obstructive lung disease: findings from the French CONSTANCES cohort.

BMC pulmonary medicine

Delmas MC, Bénézet L, Ribet C, Iwatsubo Y, Zins M, Nadif R, Roche N, Leynaert B.
PMID: 34649556
BMC Pulm Med. 2021 Oct 14;21(1):319. doi: 10.1186/s12890-021-01688-z.

BACKGROUND: The burden of undiagnosed obstructive lung disease (OLD) (mainly asthma and chronic obstructive pulmonary disease) is not fully established, and targets for corrective action are yet to be identified. We assessed the underdiagnosis of OLD and its determinants...

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Delmas MC, Bénézet L, Ribet C, et al. Underdiagnosis of obstructive lung disease: findings from the French CONSTANCES cohort. BMC Pulm Med. 2021;21(1):319doi: 10.1186/s12890-021-01688-z.
Delmas, M. C., Bénézet, L., Ribet, C., Iwatsubo, Y., Zins, M., Nadif, R., Roche, N., & Leynaert, B. (2021). Underdiagnosis of obstructive lung disease: findings from the French CONSTANCES cohort. BMC pulmonary medicine, 21(1), 319. https://doi.org/10.1186/s12890-021-01688-z
Delmas, Marie-Christine, et al. "Underdiagnosis of obstructive lung disease: findings from the French CONSTANCES cohort." BMC pulmonary medicine vol. 21,1 (2021): 319. doi: https://doi.org/10.1186/s12890-021-01688-z
Delmas MC, Bénézet L, Ribet C, Iwatsubo Y, Zins M, Nadif R, Roche N, Leynaert B. Underdiagnosis of obstructive lung disease: findings from the French CONSTANCES cohort. BMC Pulm Med. 2021 Oct 14;21(1):319. doi: 10.1186/s12890-021-01688-z. PMID: 34649556; PMCID: PMC8518215.
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Exacerbation of nontuberculous mycobacterial pulmonary disease in a patient with advanced non-small-cell lung cancer during treatment with PD-1 inhibitor and chemotherapy.

Respiratory medicine case reports

Okamoto M, Kim YH, Ouchi A, Yamaoka T, Iwamoto N, Iwatsubo S, Matsumura K, Nakamura M, Kin Y, Shiina Y, Funada Y.
PMID: 34745866
Respir Med Case Rep. 2021 Oct 21;34:101529. doi: 10.1016/j.rmcr.2021.101529. eCollection 2021.

A 69-year-old man visited our hospital due to an abnormal shadow on a chest X-ray. Chest CT showed a mass shadow in his left lower lobe accompanied by an infiltrative shadow in the right upper lobe. Thorough examination led...

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Okamoto M, Kim YH, Ouchi A, et al. Exacerbation of nontuberculous mycobacterial pulmonary disease in a patient with advanced non-small-cell lung cancer during treatment with PD-1 inhibitor and chemotherapy. Respir Med Case Rep. 2021;34:101529doi: 10.1016/j.rmcr.2021.101529.
Okamoto, M., Kim, Y. H., Ouchi, A., Yamaoka, T., Iwamoto, N., Iwatsubo, S., Matsumura, K., Nakamura, M., Kin, Y., Shiina, Y., & Funada, Y. (2021). Exacerbation of nontuberculous mycobacterial pulmonary disease in a patient with advanced non-small-cell lung cancer during treatment with PD-1 inhibitor and chemotherapy. Respiratory medicine case reports, 34101529. https://doi.org/10.1016/j.rmcr.2021.101529
Okamoto, Mariko, et al. "Exacerbation of nontuberculous mycobacterial pulmonary disease in a patient with advanced non-small-cell lung cancer during treatment with PD-1 inhibitor and chemotherapy." Respiratory medicine case reports vol. 34 (2021): 101529. doi: https://doi.org/10.1016/j.rmcr.2021.101529
Okamoto M, Kim YH, Ouchi A, Yamaoka T, Iwamoto N, Iwatsubo S, Matsumura K, Nakamura M, Kin Y, Shiina Y, Funada Y. Exacerbation of nontuberculous mycobacterial pulmonary disease in a patient with advanced non-small-cell lung cancer during treatment with PD-1 inhibitor and chemotherapy. Respir Med Case Rep. 2021 Oct 21;34:101529. doi: 10.1016/j.rmcr.2021.101529. eCollection 2021. PMID: 34745866; PMCID: PMC8555433.
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ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity.

Neurobiology of disease

An H, Litscher G, Watanabe N, Wei W, Hashimoto T, Iwatsubo T, Buchman VL, Shelkovnikova TA.
PMID: 34915152
Neurobiol Dis. 2021 Dec 14;162:105585. doi: 10.1016/j.nbd.2021.105585. Epub 2021 Dec 14.

Formation of cytoplasmic RNA-protein structures called stress granules (SGs) is a highly conserved cellular response to stress. Abnormal metabolism of SGs may contribute to the pathogenesis of (neuro)degenerative diseases such as amyotrophic lateral sclerosis (ALS). Many SG proteins are...

Cite
An H, Litscher G, Watanabe N, et al. ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity. Neurobiol Dis. 2021;162:105585doi: 10.1016/j.nbd.2021.105585.
An, H., Litscher, G., Watanabe, N., Wei, W., Hashimoto, T., Iwatsubo, T., Buchman, V. L., & Shelkovnikova, T. A. (2021). ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity. Neurobiology of disease, 162105585. https://doi.org/10.1016/j.nbd.2021.105585
An, Haiyan, et al. "ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity." Neurobiology of disease vol. 162 (2021): 105585. doi: https://doi.org/10.1016/j.nbd.2021.105585
An H, Litscher G, Watanabe N, Wei W, Hashimoto T, Iwatsubo T, Buchman VL, Shelkovnikova TA. ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity. Neurobiol Dis. 2021 Dec 14;162:105585. doi: 10.1016/j.nbd.2021.105585. Epub 2021 Dec 14. PMID: 34915152.
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