These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 26395888)

  • 1. Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADO-II) and intermediate autosomal recessive osteopetrosis (IARO) in Chinese patients.
    Pang Q; Chi Y; Zhao Z; Xing X; Li M; Wang O; Jiang Y; Liao R; Sun Y; Dong J; Xia W
    Osteoporos Int; 2016 Mar; 27(3):1047-1055. PubMed ID: 26395888
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II).
    Zhang ZL; He JW; Zhang H; Hu WW; Fu WZ; Gu JM; Yu JB; Gao G; Hu YQ; Li M; Liu YJ
    J Bone Miner Metab; 2009; 27(4):444-51. PubMed ID: 19288050
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel CLCN7 mutations cause autosomal dominant osteopetrosis type II and intermediate autosomal recessive osteopetrosis.
    Li L; Lv SS; Wang C; Yue H; Zhang ZL
    Mol Med Rep; 2019 Jun; 19(6):5030-5038. PubMed ID: 30942407
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADOII) and intermediate autosomal recessive osteopetrosis (ARO) in seven Chinese families.
    Zhang X; Wei Z; He J; Wang C; Zhang Z
    Postgrad Med; 2017 Nov; 129(8):934-942. PubMed ID: 28975865
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel mutations of CLCN7 gene in Chinese families with autosomal dominant osteopetrosis (type II).
    Zheng H; Shao C; Zheng Y; He JW; Fu WZ; Wang C; Zhang ZL
    J Bone Miner Metab; 2016 Jul; 34(4):440-6. PubMed ID: 26056022
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis.
    Frattini A; Pangrazio A; Susani L; Sobacchi C; Mirolo M; Abinun M; Andolina M; Flanagan A; Horwitz EM; Mihci E; Notarangelo LD; Ramenghi U; Teti A; Van Hove J; Vujic D; Young T; Albertini A; Orchard PJ; Vezzoni P; Villa A
    J Bone Miner Res; 2003 Oct; 18(10):1740-7. PubMed ID: 14584882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Report of two Chinese patients suffering from CLCN7-related osteopetrosis and root dysplasia.
    Xue Y; Wang W; Mao T; Duan X
    J Craniomaxillofac Surg; 2012 Jul; 40(5):416-20. PubMed ID: 21962762
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.
    Cleiren E; Bénichou O; Van Hul E; Gram J; Bollerslev J; Singer FR; Beaverson K; Aledo A; Whyte MP; Yoneyama T; deVernejoul MC; Van Hul W
    Hum Mol Genet; 2001 Dec; 10(25):2861-7. PubMed ID: 11741829
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: six novel mutations of the CLCN7 gene in twelve osteopetrosis families.
    Wang C; Zhang H; He JW; Gu JM; Hu WW; Hu YQ; Li M; Liu YJ; Fu WZ; Yue H; Ke YH; Zhang ZL
    J Bone Miner Metab; 2012 May; 30(3):338-48. PubMed ID: 21947783
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis.
    Campos-Xavier AB; Saraiva JM; Ribeiro LM; Munnich A; Cormier-Daire V
    Hum Genet; 2003 Feb; 112(2):186-9. PubMed ID: 12522560
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant osteopetrosis: clinical severity and natural history of 94 subjects with a chloride channel 7 gene mutation.
    Waguespack SG; Hui SL; Dimeglio LA; Econs MJ
    J Clin Endocrinol Metab; 2007 Mar; 92(3):771-8. PubMed ID: 17164308
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of two novel mutations on CLCN7 gene in a patient with malignant ostopetrosis.
    Bonapace G; Moricca MT; Talarico V; Graziano F; Pensabene L; Miniero R
    Ital J Pediatr; 2014 Nov; 40():90. PubMed ID: 25410126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of TCIRG1 and CLCN7 gene mutations in a patient with autosomal recessive osteopetrosis.
    Yu T; Yu Y; Wang J; Yin L; Zhou Y; Ying D; Huang R; Chen H; Wu S; Shen Y; Fu Q; Chen F
    Mol Med Rep; 2014 Apr; 9(4):1191-6. PubMed ID: 24535484
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families.
    Zhang XY; He JW; Fu WZ; Wang C; Zhang ZL
    Acta Pharmacol Sin; 2017 Nov; 38(11):1456-1465. PubMed ID: 28816234
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: report of 20 novel mutations.
    Pangrazio A; Pusch M; Caldana E; Frattini A; Lanino E; Tamhankar PM; Phadke S; Lopez AG; Orchard P; Mihci E; Abinun M; Wright M; Vettenranta K; Bariae I; Melis D; Tezcan I; Baumann C; Locatelli F; Zecca M; Horwitz E; Mansour LS; Van Roij M; Vezzoni P; Villa A; Sobacchi C
    Hum Mutat; 2010 Jan; 31(1):E1071-80. PubMed ID: 19953639
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal Dominant Osteopetrosis (ADO) Caused by a Missense Variant in the TCIRG1 Gene.
    Jodeh W; Katz AJ; Hart M; Warden SJ; Niziolek P; Alam I; Ing S; Polgreen LE; Imel EA; Econs MJ
    J Clin Endocrinol Metab; 2024 Jun; 109(7):1726-1732. PubMed ID: 38261998
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Differentially expressed genes in autosomal dominant osteopetrosis type II osteoclasts reveal known and novel pathways for osteoclast biology.
    Coudert AE; Del Fattore A; Baulard C; Olaso R; Schiltz C; Collet C; Teti A; de Vernejoul MC
    Lab Invest; 2014 Mar; 94(3):275-85. PubMed ID: 24336069
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Genetic analysis of a novel mutation resulting in autosomal dominant osteopetrosis II].
    Li X; Su N; Li C; Yang J; Du X; Chen L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):612-4. PubMed ID: 25297593
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II.
    Waguespack SG; Koller DL; White KE; Fishburn T; Carn G; Buckwalter KA; Johnson M; Kocisko M; Evans WE; Foroud T; Econs MJ
    J Bone Miner Res; 2003 Aug; 18(8):1513-8. PubMed ID: 12929941
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant osteopetrosis type II resulting from a
    Song XL; Peng LY; Wang DW; Wang H
    World J Clin Cases; 2022 Jul; 10(20):6936-6943. PubMed ID: 36051116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.