138 related articles for article (PubMed ID: 33241559)
1. The molecular structure and function of sorting nexin 10 in skeletal disorders, cancers, and other pathological conditions.
Xu J; Qiu H; Zhao J; Pavlos NJ
J Cell Physiol; 2021 Jun; 236(6):4207-4215. PubMed ID: 33241559
[TBL] [Abstract][Full Text] [Related]
2. Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis.
Xu T; Xu J; Ye Y; Wang Q; Shu X; Pei D; Liu J
Proteins; 2014 Dec; 82(12):3483-9. PubMed ID: 25212774
[TBL] [Abstract][Full Text] [Related]
3. Osteopetrorickets due to Snx10 deficiency in mice results from both failed osteoclast activity and loss of gastric acid-dependent calcium absorption.
Ye L; Morse LR; Zhang L; Sasaki H; Mills JC; Odgren PR; Sibbel G; Stanley JR; Wong G; Zamarioli A; Battaglino RA
PLoS Genet; 2015 Mar; 11(3):e1005057. PubMed ID: 25811986
[TBL] [Abstract][Full Text] [Related]
4. Snx10 and PIKfyve are required for lysosome formation in osteoclasts.
Sultana F; Morse LR; Picotto G; Liu W; Jha PK; Odgren PR; Battaglino RA
J Cell Biochem; 2020 Apr; 121(4):2927-2937. PubMed ID: 31692073
[TBL] [Abstract][Full Text] [Related]
5. An SNX10 mutation causes malignant osteopetrosis of infancy.
Aker M; Rouvinski A; Hashavia S; Ta-Shma A; Shaag A; Zenvirt S; Israel S; Weintraub M; Taraboulos A; Bar-Shavit Z; Elpeleg O
J Med Genet; 2012 Apr; 49(4):221-6. PubMed ID: 22499339
[TBL] [Abstract][Full Text] [Related]
6. Generation of induced pluripotent stem cells (ARO-iPSC1-11) from a patient with autosomal recessive osteopetrosis harboring the c.212+1G>T mutation in SNX10 gene.
Xu M; Stattin EL; Murphy M; Barry F
Stem Cell Res; 2017 Oct; 24():51-54. PubMed ID: 29034896
[TBL] [Abstract][Full Text] [Related]
7. Osteopetrosis associated with PLEKHM1 and SNX10 genes, both involved in osteoclast vesicular trafficking.
Huybrechts Y; Van Hul W
Bone; 2022 Nov; 164():116520. PubMed ID: 35981699
[TBL] [Abstract][Full Text] [Related]
8. Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis.
Udupa P; Ghosh DK; Kausthubham N; Shah H; Bartakke S; Dalal A; Girisha KM; Bhavani GS
J Hum Genet; 2023 Apr; 68(4):287-290. PubMed ID: 36526684
[TBL] [Abstract][Full Text] [Related]
9. Massive osteopetrosis caused by non-functional osteoclasts in R51Q SNX10 mutant mice.
Stein M; Barnea-Zohar M; Shalev M; Arman E; Brenner O; Winograd-Katz S; Gerstung J; Thalji F; Kanaan M; Elinav H; Stepensky P; Geiger B; Tuckermann J; Elson A
Bone; 2020 Jul; 136():115360. PubMed ID: 32278070
[TBL] [Abstract][Full Text] [Related]
10. An SNX10-dependent mechanism downregulates fusion between mature osteoclasts.
Barnea-Zohar M; Winograd-Katz SE; Shalev M; Arman E; Reuven N; Roth L; Golani O; Stein M; Thalji F; Kanaan M; Tuckermann J; Geiger B; Elson A
J Cell Sci; 2021 May; 134(9):. PubMed ID: 33975343
[TBL] [Abstract][Full Text] [Related]
11. SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.
Pangrazio A; Fasth A; Sbardellati A; Orchard PJ; Kasow KA; Raza J; Albayrak C; Albayrak D; Vanakker OM; De Moerloose B; Vellodi A; Notarangelo LD; Schlack C; Strauss G; Kühl JS; Caldana E; Lo Iacono N; Susani L; Kornak U; Schulz A; Vezzoni P; Villa A; Sobacchi C
J Bone Miner Res; 2013 May; 28(5):1041-9. PubMed ID: 23280965
[TBL] [Abstract][Full Text] [Related]
12. FKBP12: A partner of Snx10 required for vesicular trafficking in osteoclasts.
Battaglino RA; Jha P; Sultana F; Liu W; Morse LR
J Cell Biochem; 2019 Aug; 120(8):13321-13329. PubMed ID: 30887568
[TBL] [Abstract][Full Text] [Related]
13. Structure of sorting nexin 11 (SNX11) reveals a novel extended phox homology (PX) domain critical for inhibition of SNX10-induced vacuolation.
Xu J; Xu T; Wu B; Ye Y; You X; Shu X; Pei D; Liu J
J Biol Chem; 2013 Jun; 288(23):16598-16605. PubMed ID: 23615901
[TBL] [Abstract][Full Text] [Related]
14. Identification of Key Amino Acid Residues Involved in the Localization of Sorting Nexin 10 and Induction of Vacuole Formation.
Xiao B; Liu N; Hou L; Jiang M; Yao D
Biochemistry (Mosc); 2021 Nov; 86(11):1377-1387. PubMed ID: 34906048
[TBL] [Abstract][Full Text] [Related]
15. SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.
Stattin EL; Henning P; Klar J; McDermott E; Stecksen-Blicks C; Sandström PE; Kellgren TG; Rydén P; Hallmans G; Lönnerholm T; Ameur A; Helfrich MH; Coxon FP; Dahl N; Wikström J; Lerner UH
Sci Rep; 2017 Jun; 7(1):3012. PubMed ID: 28592808
[TBL] [Abstract][Full Text] [Related]
16. SNX10 is required for osteoclast formation and resorption activity.
Zhu CH; Morse LR; Battaglino RA
J Cell Biochem; 2012 May; 113(5):1608-15. PubMed ID: 22174188
[TBL] [Abstract][Full Text] [Related]
17. Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia.
Mégarbané A; Pangrazio A; Villa A; Chouery E; Maarawi J; Sabbagh S; Lefranc G; Sobacchi C
Eur J Med Genet; 2013 Jan; 56(1):32-5. PubMed ID: 23123320
[TBL] [Abstract][Full Text] [Related]
18. Sorting nexin 10 acts as a tumor suppressor in tumorigenesis and progression of colorectal cancer through regulating chaperone mediated autophagy degradation of p21
Zhang S; Hu B; You Y; Yang Z; Liu L; Tang H; Bao W; Guan Y; Shen X
Cancer Lett; 2018 Apr; 419():116-127. PubMed ID: 29355659
[TBL] [Abstract][Full Text] [Related]
19. SNX10 gene mutation in infantile malignant osteopetrosis: A case report and literature review.
Zhou T; Zeng C; Xi Q; Yang Z
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2021 Jan; 46(1):108-112. PubMed ID: 33678645
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of sorting nexin 10 prevents bone erosion in collagen-induced mouse arthritis through promoting NFATc1 degradation.
Zhou C; You Y; Shen W; Zhu YZ; Peng J; Feng HT; Wang Y; Li D; Shao WW; Li CX; Li WZ; Xu J; Shen X
Ann Rheum Dis; 2016 Jun; 75(6):1211-8. PubMed ID: 26141367
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
