244 related articles for article (PubMed ID: 36881265)
1. SP7: from Bone Development to Skeletal Disease.
Wang JS; Tokavanich N; Wein MN
Curr Osteoporos Rep; 2023 Apr; 21(2):241-252. PubMed ID: 36881265
[TBL] [Abstract][Full Text] [Related]
2. Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment.
Fiscaletti M; Biggin A; Bennetts B; Wong K; Briody J; Pacey V; Birman C; Munns CF
Bone; 2018 May; 110():66-75. PubMed ID: 29382611
[TBL] [Abstract][Full Text] [Related]
3. Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variant.
Ludwig K; Ward LM; Khan N; Robinson ME; Miranda V; Bardai G; Moffatt P; Rauch F
Bone; 2022 Jul; 160():116400. PubMed ID: 35367406
[TBL] [Abstract][Full Text] [Related]
4. Biallelic variants in four genes underlying recessive osteogenesis imperfecta.
Hayat A; Hussain S; Bilal M; Kausar M; Almuzzaini B; Abbas S; Tanveer A; Khan A; Siddiqi S; Foo JN; Ahmad F; Khan F; Khan B; Anees M; Mäkitie O; Alfadhel M; Ahmad W; Umair M
Eur J Med Genet; 2020 Aug; 63(8):103954. PubMed ID: 32413570
[TBL] [Abstract][Full Text] [Related]
5. Long-term follow-up of severe autosomal recessive SP7-related bone disorder.
Gauthier LW; Fontanges E; Chapurlat R; Collet C; Rossi M
Bone; 2024 Feb; 179():116953. PubMed ID: 37918503
[TBL] [Abstract][Full Text] [Related]
6. Sp7 Action in the Skeleton: Its Mode of Action, Functions, and Relevance to Skeletal Diseases.
Hojo H; Ohba S
Int J Mol Sci; 2022 May; 23(10):. PubMed ID: 35628456
[TBL] [Abstract][Full Text] [Related]
7. Osteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formation.
Marini JC; Reich A; Smith SM
Curr Opin Pediatr; 2014 Aug; 26(4):500-7. PubMed ID: 25007323
[TBL] [Abstract][Full Text] [Related]
8. A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorder.
Lui JC; Raimann A; Hojo H; Dong L; Roschger P; Kikani B; Wintergerst U; Fratzl-Zelman N; Jee YH; Haeusler G; Baron J
Nat Commun; 2022 Feb; 13(1):700. PubMed ID: 35121733
[TBL] [Abstract][Full Text] [Related]
9. Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta.
Lapunzina P; Aglan M; Temtamy S; Caparrós-Martín JA; Valencia M; Letón R; Martínez-Glez V; Elhossini R; Amr K; Vilaboa N; Ruiz-Perez VL
Am J Hum Genet; 2010 Jul; 87(1):110-4. PubMed ID: 20579626
[TBL] [Abstract][Full Text] [Related]
10.
Chen Z; Song Z; Yang J; Huang J; Jiang H
J Biosci; 2019 Dec; 44(6):. PubMed ID: 31894108
[TBL] [Abstract][Full Text] [Related]
11. Inactivation of Ihh in Sp7-Expressing Cells Inhibits Osteoblast Proliferation, Differentiation, and Bone Formation, Resulting in a Dwarfism Phenotype with Severe Skeletal Dysplasia in Mice.
Wang Y; Dong Z; Yang R; Zong S; Wei X; Wang C; Guo L; Sun J; Li H; Li P
Calcif Tissue Int; 2022 Nov; 111(5):519-534. PubMed ID: 35731246
[TBL] [Abstract][Full Text] [Related]
12. Control of osteocyte dendrite formation by Sp7 and its target gene osteocrin.
Wang JS; Kamath T; Mazur CM; Mirzamohammadi F; Rotter D; Hojo H; Castro CD; Tokavanich N; Patel R; Govea N; Enishi T; Wu Y; da Silva Martins J; Bruce M; Brooks DJ; Bouxsein ML; Tokarz D; Lin CP; Abdul A; Macosko EZ; Fiscaletti M; Munns CF; Ryder P; Kost-Alimova M; Byrne P; Cimini B; Fujiwara M; Kronenberg HM; Wein MN
Nat Commun; 2021 Nov; 12(1):6271. PubMed ID: 34725346
[TBL] [Abstract][Full Text] [Related]
13. Specificity Protein 7 Is Required for Proliferation and Differentiation of Ameloblasts and Odontoblasts.
Bae JM; Clarke JC; Rashid H; Adhami MD; McCullough K; Scott JS; Chen H; Sinha KM; de Crombrugghe B; Javed A
J Bone Miner Res; 2018 Jun; 33(6):1126-1140. PubMed ID: 29405385
[TBL] [Abstract][Full Text] [Related]
14. Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7).
Whyte MP; Campeau PM; McAlister WH; Roodman GD; Kurihara N; Nenninger A; Duan S; Gottesman GS; Bijanki VN; Sedighi H; Veis DJ; Mumm S
Bone; 2020 Aug; 137():115364. PubMed ID: 32298837
[TBL] [Abstract][Full Text] [Related]
15. Atf7ip Inhibits Osteoblast Differentiation via Negative Regulation of the Sp7 Transcription Factor.
Hu G; Shi X; Qu X; Han C; Hu A; Jia Z; Yang J; Liu H; Wu Y
Int J Mol Sci; 2023 Feb; 24(5):. PubMed ID: 36901736
[TBL] [Abstract][Full Text] [Related]
16. RNA sequencing analysis reveals increased expression of interferon signaling genes and dysregulation of bone metabolism affecting pathways in the whole blood of patients with osteogenesis imperfecta.
Zhytnik L; Maasalu K; Reimann E; Märtson A; Kõks S
BMC Med Genomics; 2020 Nov; 13(1):177. PubMed ID: 33228694
[TBL] [Abstract][Full Text] [Related]
17. [Mutations of noncollagen genes in osteogenesis imperfecta--implications of the gene products in collagen biosynthesis and pathogenesis of disease].
Galicka A
Postepy Hig Med Dosw (Online); 2012 Jun; 66():359-71. PubMed ID: 22706122
[TBL] [Abstract][Full Text] [Related]
18. Osterix/Sp7 limits cranial bone initiation sites and is required for formation of sutures.
Kague E; Roy P; Asselin G; Hu G; Simonet J; Stanley A; Albertson C; Fisher S
Dev Biol; 2016 May; 413(2):160-72. PubMed ID: 26992365
[TBL] [Abstract][Full Text] [Related]
19. Skeletal Deformities in Osterix-Cre;Tgfbr2
Corps K; Stanwick M; Rectenwald J; Kruggel A; Peters SB
Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34202311
[TBL] [Abstract][Full Text] [Related]
20. MiR-96 regulates bone metabolism by targeting osterix.
Liu H; Liu Q; Wu XP; He HB; Fu L
Clin Exp Pharmacol Physiol; 2018 Jun; 45(6):602-613. PubMed ID: 29288578
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
