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Modulation of Endocannabinoid Tone in Osteoblastic Differentiation of MC3T3-E1 Cells and in Mouse Bone Tissue over Time.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 5, p. 1199, doi. 10.3390/cells10051199
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- Article
ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 10, p. 1974, doi. 10.1002/jbmr.3993
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- Article
The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone.
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- Journal of Bone & Mineral Research, 2020, v. 35, n. 8, p. 1387, doi. 10.1002/jbmr.3964
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- Article
Clinical Characteristics and Evolution of Giant Cell Tumor Occurring in Paget's Disease of Bone.
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- Journal of Bone & Mineral Research, 2015, v. 30, n. 2, p. 257, doi. 10.1002/jbmr.2349
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- Article
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.
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- Journal of Bone & Mineral Research, 2013, v. 28, n. 11, p. 2338, doi. 10.1002/jbmr.1975
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- Article
Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree.
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- Journal of Bone & Mineral Research, 2013, v. 28, n. 2, p. 341, doi. 10.1002/jbmr.1750
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- Article
A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease.
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- Journal of Bone & Mineral Research, 2012, v. 27, n. 2, p. 443, doi. 10.1002/jbmr.542
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- Article
Comparison of intravenous and intramuscular neridronate regimens for the treatment of paget disease of bone.
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- Journal of Bone & Mineral Research, 2011, v. 26, n. 3, p. 512, doi. 10.1002/jbmr.237
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- Article
SQSTM1 Gene Analysis and Gene-Environment Interaction in Paget's Disease of Bone.
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- Journal of Bone & Mineral Research, 2010, v. 25, n. 6, p. 1375, doi. 10.1002/jbmr.31
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- Article
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population.
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- Indian Journal of Otolaryngology & Head & Neck Surgery, 2014, v. 66, n. 3, p. 297, doi. 10.1007/s12070-014-0706-6
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- Article
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts.
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- Neurogenetics, 2008, v. 9, n. 1, p. 25, doi. 10.1007/s10048-007-0109-x
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- Article
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3654, doi. 10.1093/hmg/ddt215
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- Article
Association of a GRIA3 Gene Polymorphism With Migraine in an Australian Case-Control Cohort.
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- Headache: The Journal of Head & Face Pain, 2013, v. 53, n. 8, p. 1245, doi. 10.1111/head.12151
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- Article
DDXIIL: a novel transcript family emerging from human subtelomeric regions.
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- BMC Genomics, 2009, v. 10, p. 250, doi. 10.1186/1471-2164-10-250
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- Article
Bone Turnover and the Osteoprotegerin–RANKL Pathway in Tumor-Induced Osteomalacia: A Longitudinal Study of Five Cases.
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- Calcified Tissue International, 2009, v. 85, n. 4, p. 293, doi. 10.1007/s00223-009-9275-1
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- Article
Vitamin D receptor gene polymorphisms predict acquired resistance to clodronate treatment in patients with Paget's disease of bone.
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- 2008
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- Publication type:
- journal article
Hypovitaminosis D and Organ Damage In Patients With Arterial Hypertension: A Multicenter Double Blind Randomised Controlled Trial of Cholecalciferol Supplementation (HYPODD)
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- 2015
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- Publication type:
- Journal Article
Hypovitaminosis D and Organ Damage In Patients With Arterial Hypertension: A Multicenter Double Blind Randomised Controlled Trial of Cholecalciferol Supplementation (HYPODD).
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- High Blood Pressure & Cardiovascular Prevention, 2015, v. 22, n. 2, p. 135, doi. 10.1007/s40292-015-0080-9
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- Article
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
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- Nature Genetics, 2011, v. 43, n. 7, p. 685, doi. 10.1038/ng.845
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- Article
FSHR gene polymorphisms influence bone mineral density and bone turnover in postmenopausal women.
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- European Journal of Endocrinology, 2010, v. 163, n. 1, p. 165, doi. 10.1530/EJE-10-0043
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- Article
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.
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- 2013
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- Publication type:
- Journal Article
Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.
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- Italian Journal of Pediatrics, 2013, v. 39, n. 1, p. 58, doi. 10.1186/1824-7288-39-58
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- Publication type:
- Article
The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location.
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- 2018
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- Publication type:
- journal article
The melatonin receptor 1A (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis.
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- Nephrology Dialysis Transplantation, 2012, v. 27, n. 1, p. 210, doi. 10.1093/ndt/gfr216
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- Article
Profilin 1 deficiency drives mitotic defects and reduces genome stability.
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- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-022-04392-8
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- Article
A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model.
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- Bone Research, 2023, v. 11, n. 1, p. 1, doi. 10.1038/s41413-023-00250-3
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- Article
ATP1A2 gene mutations are not present in two sisters with basilar-type migraine associated with menses.
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- Neurological Sciences, 2008, v. 29, n. 2, p. 113, doi. 10.1007/s10072-008-0870-0
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- Article
piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene.
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- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022727
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- Article
Novel autophagic vacuolar myopathies: Phenotype and genotype features.
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- Neuropathology & Applied Neurobiology, 2021, v. 47, n. 5, p. 664, doi. 10.1111/nan.12690
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- Article
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship.
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- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-159
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- Article
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.
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- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-91
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- Publication type:
- Article
Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship.
- Published in:
- 2013
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- Publication type:
- journal article
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.
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- 2013
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- Publication type:
- journal article
Evidence for epistatic interaction between VDR and SLC13A2 genes in the pathogenesis of hypocitraturia in recurrent calcium oxalate stone formers.
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- Journal of Nephrology (JNonline), 2017, v. 30, n. 3, p. 411, doi. 10.1007/s40620-016-0348-8
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- Publication type:
- Article
Common variants in the regulative regions ofGRIA1 and GRIA3 receptor genes are associatedwith migraine susceptibility.
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- BMC Medical Genetics, 2010, v. 11, p. 103, doi. 10.1186/1471-2350-11-103
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- Article
Identification of a novel candidate gene, CASC2, in a region of common allelic loss at chromosome 10q26 in human endometrial cancer.
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- Human Mutation, 2004, v. 23, n. 4, p. 318, doi. 10.1002/humu.20015
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- Article
A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases.
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- Human Molecular Genetics, 1999, v. 8, n. 1, p. 61, doi. 10.1093/hmg/8.1.61
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- Article
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere.
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- Human Molecular Genetics, 1998, v. 7, n. 3, p. 407, doi. 10.1093/hmg/7.3.407
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- Publication type:
- Article