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Canadian Journal of Neurological Sciences, ISSN 0317-1671, 01/2018, Volume 45, Issue 1, pp. 62 - 67
Journal Article
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, ISSN 1735-5338, 11/2016, Volume 19, Issue 8, pp. 79 - 87
Abstract Background: Osteoporosis is describesd as a disorder and skeletal disease that decrease bone strength and increases the risk of a bone fractures.... 
Osteoporosis | LRP4 | Polymorphism
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2011, Volume 69, Issue 2, pp. 418 - 422
Journal Article
Revue de Medecine Interne, ISSN 0248-8663, 2014, Volume 35, Issue 7, pp. 413 - 420
Myasthenia gravis is characterized by muscle weakness and abnormal fatigability. It is an autoimmune disease caused by the presence of antibodies against... 
MuSK | LRP4 | Acetylcholine receptor | Thymus
Journal Article
Nature Reviews Neuroscience, ISSN 1471-003X, 12/2008, Volume 9, Issue 12, pp. 886 - 886
Journal Article
Journal Article
Journal Article
Internal Medicine, ISSN 0918-2918, 2016, Volume 55, Issue 22, pp. 3361 - 3363
We herein report the case of a 72-year-old man demonstrating myasthenia gravis (MG) with a dropped head and acute respiratory insufficiency. There was no... 
myasthenia gravis | steroid pulse therapy | acute respiratory insufficiency | anti-LRP4 antibodies | dropped head | Anti-LRP4 antibodies | Dropped head | Steroid pulse therapy | Myasthenia gravis | Acute respiratory insufficiency | AUTOANTIBODIES | MEDICINE, GENERAL & INTERNAL | PROTEIN 4 | LRP4 ANTIBODIES | RECEPTOR
Journal Article
by He, XL
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, ISSN 1570-9639, 10/2013, Volume 1834, Issue 10, pp. 2158 - 2159
Journal Article
Current Opinion in Neurology, ISSN 1350-7540, 2016, Volume 29, Issue 5, pp. 565 - 571
Purpose of reviewCongenital myasthenic syndromes (CMS) are a group of heterogeneous inherited disorders caused by mutations in genes encoding proteins... 
Congenital myasthenic syndromes | Collagen 13A1 | N-glycosylation pathway | Salbutamol, presynaptic | collagen 13A1 | AGRIN | MUSK | presynaptic | salbutamol | GDP-MANNOSE PYROPHOSPHORYLASE | LRP4 | GLYCOSYLATION | NEUROSCIENCES | DEFICIENCY | CLINICAL NEUROLOGY | NEUROMUSCULAR-TRANSMISSION | LIMB | MUTATIONS CAUSE | congenital myasthenic syndromes
Journal Article
Journal of Autoimmunity, ISSN 0896-8411, 2013, Volume 52, pp. 139 - 145
Journal Article
TOXINS, ISSN 2072-6651, 07/2019, Volume 11, Issue 7, p. 428
Sclerostin is a well-known inhibitor of bone formation that acts on Wnt /fi -catenin signaling. This manuscript considers the possible role of sclerostin in... 
chronic kidney disease | mineral abnormalities | rat model | PROTEIN | vascular calcification | INCREASES | SERUM SCLEROSTIN | LRP4 | TOXICOLOGY | bone disease
Journal Article
The Journal of neuroscience : the official journal of the Society for Neuroscience, ISSN 0270-6474, 10/2018, Volume 38, Issue 41, pp. 8860 - 8873
During aging, acetylcholine receptor (AChR) clusters become fragmented and denervated at the neuromuscular junction (NMJ). Under-pinning molecular mechanisms... 
LRP4 | aging | SGα | neuromuscular junction | AGRIN RECEPTOR | DYSTROPHIN-GLYCOPROTEIN COMPLEX | RAT MUSCLE | DEFICIENT MICE | NEUROSCIENCES | END-PLATES | SG alpha | MOTOR UNIT | TYROSINE KINASE MUSK | SKELETAL-MUSCLE FIBERS | DUCHENNE MUSCULAR-DYSTROPHY | MYASTHENIA-GRAVIS
Journal Article
by Zhang, DD and Park, BM and Kang, M and Nam, H and Kim, EJ and Bae, C and Lim, SK
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, ISSN 0006-291X, 04/2016, Volume 472, Issue 3, pp. 471 - 476
Sclerostin, encoded by the Sost gene, is mainly produced by osteocytes in bone and antagonizes the Wnt/beta-catenin signaling pathway, which is a requisite for... 
BIOCHEMISTRY & MOLECULAR BIOLOGY | GENOMIC INTEGRATION | LRP4 | Serum sclerostin | DELETION | FRACTURE | BIOPHYSICS | BONE-FORMATION | SOST GENE | ROMOSOZUMAB | Phi C31 integrase | Sost | Bone | MUTATIONS | POSTMENOPAUSAL WOMEN
Journal Article
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