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Best matches for fracture AND COL1A2:

Osteogenesis imperfecta. Marini JC et al. Nat Rev Dis Primers. (2017)

Osteogenesis imperfecta: diagnosis and treatment. Palomo T et al. Curr Opin Endocrinol Diabetes Obes. (2017)

Bone turnover: Biology and assessment tools. Szulc P et al. Best Pract Res Clin Endocrinol Metab. (2018)

Search results

Items: 1 to 20 of 1055

1.

Melatonin promotes osteoblastic differentiation and regulates PDGF/AKT signaling pathway.

Zhu G, Ma B, Dong P, Shang J, Gu X, Zi Y.

Cell Biol Int. 2019 Sep 19. doi: 10.1002/cbin.11240. [Epub ahead of print]

PMID:
31535749
2.

COL1A1/2 Osteogenesis Imperfecta.

Steiner RD, Basel D.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2005 Jan 28 [updated 2019 Sep 19].

3.

Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research.

Tauer JT, Robinson ME, Rauch F.

JBMR Plus. 2019 Feb 20;3(8):e10174. doi: 10.1002/jbm4.10174. eCollection 2019 Aug. Review.

4.

Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation.

Mumm S, Gottesman GS, Wenkert D, Campeau PM, Nenninger A, Huskey M, Bijanki VN, Veis DJ, Barnes AM, Marini JC, Stolina M, Zhang F, McAlister WH, Whyte MP.

Bone. 2019 Aug 28:115047. doi: 10.1016/j.bone.2019.115047. [Epub ahead of print]

PMID:
31472299
5.

COL1A1/2 Pathogenic Variants and Phenotype Characteristics in Ukrainian Osteogenesis Imperfecta Patients.

Zhytnik L, Maasalu K, Pashenko A, Khmyzov S, Reimann E, Prans E, Kõks S, Märtson A.

Front Genet. 2019 Aug 9;10:722. doi: 10.3389/fgene.2019.00722. eCollection 2019.

6.

Osteogenesis imperfecta in Brazilian patients.

Trancozo M, Moraes MVD, Silva DA, Soares JAM, Barbirato C, Almeida MG, Santos LR, Rebouças MRGO, Akel AN Jr, Sipolatti V, Nunes VRR, Errera FIV, Aguena M, Passos-Bueno MR, Paula F.

Genet Mol Biol. 2019 Apr-Jun;42(2):344-350. doi: 10.1590/1678-4685-GMB-2018-0043. Epub 2019 Aug 15.

7.

Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.

Ohata Y, Takeyari S, Nakano Y, Kitaoka T, Nakayama H, Bizaoui V, Yamamoto K, Miyata K, Yamamoto K, Fujiwara M, Kubota T, Michigami T, Yamamoto K, Yamamoto T, Namba N, Ebina K, Yoshikawa H, Ozono K.

Osteoporos Int. 2019 Jul 29. doi: 10.1007/s00198-019-05076-6. [Epub ahead of print]

PMID:
31363794
8.

Paracrine effects of living human bone particles on the osteogenic differentiation of mesenchymal stem cells.

Atasoy-Zeybek A, Ivkovic A, Beyzadeoglu T, Onal A, Evans CH, Kose GT.

Eur Cell Mater. 2019 Jul 23;38:14-22. doi: 10.22203/eCM.v038a02.

9.

Sesamin Promotes Osteoblastic Differentiation and Protects Rats from Osteoporosis.

Ma ZP, Zhang ZF, Yang YF, Yang Y.

Med Sci Monit. 2019 Jul 17;25:5312-5320. doi: 10.12659/MSM.915529.

10.

Ventricular Septal Defect Closure in a Neonate with Osteogenesis Imperfecta.

Jang WS, Choi HJ, Kim JB, Kim JH.

Korean J Thorac Cardiovasc Surg. 2019 Jun;52(3):162-164. doi: 10.5090/kjtcs.2019.52.3.162. Epub 2019 Jun 5.

11.

Splice receptor-site mutation c.697-2A>G of the COL1A1 gene in a Chinese family with osteogenesis imperfecta.

Zhai N, Lu Y, Wang Y, Zhang S, Peng C, Zhang S, Li T, Chen M, Liu J, Fang F, Ren X, Han J.

Intractable Rare Dis Res. 2019 May;8(2):150-153. doi: 10.5582/irdr.2019.01046.

12.

Effects of human umbilical cord mesenchymal stem cells-derived exosomes on fracture healing in rats through the Wnt signaling pathway.

Zhou J, Liu HX, Li SH, Gong YS, Zhou MW, Zhang JH, Zhu GY.

Eur Rev Med Pharmacol Sci. 2019 Jun;23(11):4954-4960. doi: 10.26355/eurrev_201906_18086.

13.

Mendelian bone fragility disorders.

Robinson ME, Rauch F.

Bone. 2019 Sep;126:11-17. doi: 10.1016/j.bone.2019.04.021. Epub 2019 Apr 27.

PMID:
31039433
14.

A novel Ser40Trp variant in IFITM5 in a family with osteogenesis imperfecta and review of the literature.

Lim JY, Bhatia NS, Vasanwala RF, Chay PL, Lim KBL, Khoo PC, Schwarze U, Jamuar SS.

Clin Dysmorphol. 2019 Jul;28(3):120-125. doi: 10.1097/MCD.0000000000000279.

PMID:
30985308
15.

Osteogenesis Imperfecta Due to Combined Heterozygous Mutations in Both COL1A1 and COL1A2, Coexisting With Pituitary Stalk Interruption Syndrome.

Wang D, Zhang M, Guan H, Wang X.

Front Endocrinol (Lausanne). 2019 Mar 28;10:193. doi: 10.3389/fendo.2019.00193. eCollection 2019.

16.

Hypercholesterolaemia increases the risk of high‑turnover osteoporosis in men.

Zhou Y, Deng T, Zhang H, Guan Q, Zhao H, Yu C, Shao S, Zhao M, Xu J.

Mol Med Rep. 2019 Jun;19(6):4603-4612. doi: 10.3892/mmr.2019.10131. Epub 2019 Apr 4.

17.

A Case of Osteogenesis Imperfecta Type II With Additional Balanced Translocation t(1;20)(p13;p11.2).

Majeed NK, Oramas D, Lindgren V, Garzon S, Wiley DE, Enakpene C, Emmadi R.

Fetal Pediatr Pathol. 2019 Jun;38(3):263-271. doi: 10.1080/15513815.2019.1579877. Epub 2019 Apr 3.

PMID:
30942118
18.

Neurosurgical Implications of Osteogenesis Imperfecta in a Child after Fall: Case Illustration.

Moscote-Salazar LR, Koller O, Valenzuela S, Narvaez-Rojas A, Satyarthee GD, Mo-Carrascal J, Maraby J.

J Pediatr Neurosci. 2018 Oct-Dec;13(4):459-461. doi: 10.4103/JPN.JPN_9_18.

19.

NOVEL MUTATIONS IN THE WNT1, TMEM38B, P4HB, AND PLS3 GENES IN FOUR UNRELATED CHINESE FAMILIES WITH OSTEOGENESIS IMPERFECTA.

Cao YJ, Zhang H, Zhang ZL.

Endocr Pract. 2019 Mar;25(3):230-241. doi: 10.4158/EP-2018-0443.

PMID:
30913006
20.

Complex spine deformities in young patients with severe osteogenesis imperfecta: current concepts review.

Castelein RM, Hasler C, Helenius I, Ovadia D, Yazici M; EPOS Spine Study Group.

J Child Orthop. 2019 Feb 1;13(1):22-32. doi: 10.1302/1863-2548.13.180185. Review.

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