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92 results

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Page 1
The Pathology of Amyloidosis in Classification: A Review.
Picken MM. Picken MM. Acta Haematol. 2020;143(4):322-334. doi: 10.1159/000506696. Epub 2020 May 11. Acta Haematol. 2020. PMID: 32392555 Free article. Review.
Other hereditary amyloidoses include AFib, several amyloidoses derived from apolipoproteins, AGel, ALys, etc. In a dialysis setting, systemic amyloid derived from beta2 microglobulin (Abeta2M) should be considered, although a very rare hereditary variant has also been repo …
Other hereditary amyloidoses include AFib, several amyloidoses derived from apolipoproteins, AGel, ALys, etc. In a dialysis setting, …
Characteristics and applications of alginate lyases: A review.
Cheng D, Jiang C, Xu J, Liu Z, Mao X. Cheng D, et al. Int J Biol Macromol. 2020 Dec 1;164:1304-1320. doi: 10.1016/j.ijbiomac.2020.07.199. Epub 2020 Jul 31. Int J Biol Macromol. 2020. PMID: 32745554 Review.
In view of their important functions, an increasing number of Alys have been isolated and characterized. For better application, a comprehensive understanding of Alys is essential. ...In addition, applications of Alys have been illustrated with examples. This …
In view of their important functions, an increasing number of Alys have been isolated and characterized. For better application, a co …
Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review.
Benyamine A, Bernard-Guervilly F, Tummino C, Macagno N, Daniel L, Valleix S, Granel B. Benyamine A, et al. Clin Rheumatol. 2017 Nov;36(11):2623-2628. doi: 10.1007/s10067-017-3839-7. Epub 2017 Sep 30. Clin Rheumatol. 2017. PMID: 28963698 Review.
In the present observation, we extend the phenotypic heterogeneity of ALys to the tracheobronchial tree with histologically proven bronchial ALys-amyloid deposits. ...Due to diffuse organs involvement related to ALys, it is important not to misdiagnose ALy …
In the present observation, we extend the phenotypic heterogeneity of ALys to the tracheobronchial tree with histologically proven br …
Computational modeling in pregnancy biomechanics research.
Clark AR, Yoshida K, Oyen ML. Clark AR, et al. J Mech Behav Biomed Mater. 2022 Apr;128:105099. doi: 10.1016/j.jmbbm.2022.105099. Epub 2022 Jan 24. J Mech Behav Biomed Mater. 2022. PMID: 35121424 Review.
Gastrointestinal amyloidosis: an often unexpected finding with systemic implications.
Hagen CE, Dasari S, Theis JD, Rech KL, Dao LN, Howard MT, Dispenzieri A, Chiu A, Dalland JC, Kurtin PJ, Gertz MA, Kourelis TV, Muchtar E, Vrana JA, McPhail ED. Hagen CE, et al. Hum Pathol. 2023 Sep;139:27-36. doi: 10.1016/j.humpath.2023.06.007. Epub 2023 Jun 28. Hum Pathol. 2023. PMID: 37390975
Twelve amyloid types were identified, including AL (77.9%), ATTR (11.3%), AA (6.6%), AH (1.1%), AApoAIV (1.1%), AEFEMP1 (0.7%), ALys (0.4%), AApoAI (0.4%), ALECT2 (0.2%), Abeta2M (0.1%), AGel (0.1%), and AFib (<0.1%). ...
Twelve amyloid types were identified, including AL (77.9%), ATTR (11.3%), AA (6.6%), AH (1.1%), AApoAIV (1.1%), AEFEMP1 (0.7%), ALys …
ALys amyloidosis caused by compound heterozygosity in exon 2 (Thr70Asn) and exon 4 (Trp112Arg) of the lysozyme gene.
Röcken C, Becker K, Fändrich M, Schroeckh V, Stix B, Rath T, Kähne T, Dierkes J, Roessner A, Albert FW. Röcken C, et al. Hum Mutat. 2006 Jan;27(1):119-20. doi: 10.1002/humu.9393. Hum Mutat. 2006. PMID: 16329101
This type of hereditary ALys amyloidosis is characterized by extended amyloid deposits in the upper gastrointestinal tract, entire colon, and kidney, leading to gastrointestinal bleeding. ...Interestingly, this form of ALys amyloidosis is also characterized by the o …
This type of hereditary ALys amyloidosis is characterized by extended amyloid deposits in the upper gastrointestinal tract, entire co …
Hereditary lysozyme amyloidosis -- phenotypic heterogeneity and the role of solid organ transplantation.
Sattianayagam PT, Gibbs SD, Rowczenio D, Pinney JH, Wechalekar AD, Gilbertson JA, Hawkins PN, Lachmann HJ, Gillmore JD. Sattianayagam PT, et al. J Intern Med. 2012 Jul;272(1):36-44. doi: 10.1111/j.1365-2796.2011.02470.x. Epub 2011 Nov 15. J Intern Med. 2012. PMID: 21988333 Free article.
OBJECTIVES: Lysozyme amyloidosis (ALys) is a form of hereditary systemic non-neuropathic amyloidosis, which is inherited in an autosomal dominant fashion. ...The aim of this study is to describe the phenotype and outcome of patients with ALys including the role of s …
OBJECTIVES: Lysozyme amyloidosis (ALys) is a form of hereditary systemic non-neuropathic amyloidosis, which is inherited in an autoso …
Hemin is able to disaggregate lysozyme amyloid fibrils into monomers.
Sonavane S, Haider SZ, Kumar A, Ahmad B. Sonavane S, et al. Biochim Biophys Acta Proteins Proteom. 2017 Nov;1865(11 Pt A):1315-1325. doi: 10.1016/j.bbapap.2017.07.017. Epub 2017 Aug 18. Biochim Biophys Acta Proteins Proteom. 2017. PMID: 28827166
Lysozyme amyloidosis (ALys) is a disease of the gastrointestinal tract, liver and kidneys, which is caused by the accumulation of insoluble fibrils of lysozyme in the tissues of above organs. The ALys can be cured by disintegration and clearance of the fibrils from …
Lysozyme amyloidosis (ALys) is a disease of the gastrointestinal tract, liver and kidneys, which is caused by the accumulation of ins …
92 results