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1967
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1967 2
1968 1
1969 3
1970 4
1972 4
1974 2
1975 1
1976 1
1977 1
1978 1
1979 1
1980 1
1981 1
1982 5
1983 4
1984 6
1985 3
1986 4
1987 2
1988 3
1989 7
1990 5
1991 10
1992 4
1993 11
1994 6
1995 9
1996 6
1997 3
1998 10
1999 9
2000 8
2001 15
2002 16
2003 13
2004 14
2005 19
2006 17
2007 17
2008 17
2009 26
2010 14
2011 11
2012 17
2013 15
2014 10
2015 11
2016 10
2017 4
2018 15
2019 9
2020 10
2021 17
2022 13
2023 11
2024 5
2025 0

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432 results

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Page 1
Fate decision of mesenchymal stem cells: adipocytes or osteoblasts?
Chen Q, Shou P, Zheng C, Jiang M, Cao G, Yang Q, Cao J, Xie N, Velletri T, Zhang X, Xu C, Zhang L, Yang H, Hou J, Wang Y, Shi Y. Chen Q, et al. Cell Death Differ. 2016 Jul;23(7):1128-39. doi: 10.1038/cdd.2015.168. Epub 2016 Feb 12. Cell Death Differ. 2016. PMID: 26868907 Free PMC article. Review.
The dysregulation of the adipo-osteogenic balance has been linked to several pathophysiologic processes, such as aging, obesity, osteopenia, osteopetrosis, and osteoporosis. Thus, the regulation of MSC differentiation has increasingly attracted great attention in recent ye …
The dysregulation of the adipo-osteogenic balance has been linked to several pathophysiologic processes, such as aging, obesity, osteopenia, …
Autosomal dominant osteopetrosis.
Polgreen LE, Imel EA, Econs MJ. Polgreen LE, et al. Bone. 2023 May;170:116723. doi: 10.1016/j.bone.2023.116723. Epub 2023 Feb 28. Bone. 2023. PMID: 36863500 Free PMC article. Review.
Autosomal dominant osteopetrosis (ADO) is the most common form of osteopetrosis. ADO is characterized by generalized osteosclerosis along with characteristic radiographic features such as a "bone-in-bone" appearance of long bones and sclerosis of the superior and in …
Autosomal dominant osteopetrosis (ADO) is the most common form of osteopetrosis. ADO is characterized by generalized osteoscle …
Osteopetrosis.
Stark Z, Savarirayan R. Stark Z, et al. Orphanet J Rare Dis. 2009 Feb 20;4:5. doi: 10.1186/1750-1172-4-5. Orphanet J Rare Dis. 2009. PMID: 19232111 Free PMC article. Review.
Osteopetrosis ("marble bone disease") is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterized by increased bone density on radiographs. The overall incidence of these conditions is difficult to estimate but autosomal recessiv
Osteopetrosis ("marble bone disease") is a descriptive term that refers to a group of rare, heritable disorders of the skeleton chara
Diagnosis and Management of Osteopetrosis: Consensus Guidelines From the Osteopetrosis Working Group.
Wu CC, Econs MJ, DiMeglio LA, Insogna KL, Levine MA, Orchard PJ, Miller WP, Petryk A, Rush ET, Shoback DM, Ward LM, Polgreen LE. Wu CC, et al. J Clin Endocrinol Metab. 2017 Sep 1;102(9):3111-3123. doi: 10.1210/jc.2017-01127. J Clin Endocrinol Metab. 2017. PMID: 28655174 Review.
BACKGROUND: Osteopetrosis encompasses a group of rare metabolic bone diseases characterized by impaired osteoclast activity or development, resulting in high bone mineral density. ...We suggest that calcitriol should not be used in high doses and instead recommend symptom- …
BACKGROUND: Osteopetrosis encompasses a group of rare metabolic bone diseases characterized by impaired osteoclast activity or develo …
Bone resorption by osteoclasts.
Teitelbaum SL. Teitelbaum SL. Science. 2000 Sep 1;289(5484):1504-8. doi: 10.1126/science.289.5484.1504. Science. 2000. PMID: 10968780 Review.
CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease.
Jentsch TJ, Pusch M. Jentsch TJ, et al. Physiol Rev. 2018 Jul 1;98(3):1493-1590. doi: 10.1152/physrev.00047.2017. Physiol Rev. 2018. PMID: 29845874 Free article. Review.
These pathologies include neurodegeneration, leukodystrophy, mental retardation, deafness, blindness, myotonia, hyperaldosteronism, renal salt loss, proteinuria, kidney stones, male infertility, and osteopetrosis. In this review, emphasis is laid on biophysical structure-f …
These pathologies include neurodegeneration, leukodystrophy, mental retardation, deafness, blindness, myotonia, hyperaldosteronism, renal sa …
Genetics of Osteopetrosis.
Palagano E, Menale C, Sobacchi C, Villa A. Palagano E, et al. Curr Osteoporos Rep. 2018 Feb;16(1):13-25. doi: 10.1007/s11914-018-0415-2. Curr Osteoporos Rep. 2018. PMID: 29335834 Review.
Osteopetrosis is clinically and genetically heterogeneous, and a precise molecular classification is relevant for prognosis and treatment. ...Yet, the causative mutation is unknown in some patients, indicating that the genetics of osteopetrosis still deserves intens
Osteopetrosis is clinically and genetically heterogeneous, and a precise molecular classification is relevant for prognosis and treat
Imaging in osteopetrosis.
Calder AD, Arulkumaran S, D'Arco F. Calder AD, et al. Bone. 2022 Dec;165:116560. doi: 10.1016/j.bone.2022.116560. Epub 2022 Sep 15. Bone. 2022. PMID: 36116759 Review.
Imaging investigations are critical in the management of children with suspected and confirmed osteopetrosis. In severe cases, imaging can provide rapid confirmation of the diagnosis, whilst in milder cases, imaging findings may be the first or only indicators of the disea …
Imaging investigations are critical in the management of children with suspected and confirmed osteopetrosis. In severe cases, imagin …
Osteoclasts: Other functions.
Park-Min KH, Lorenzo J. Park-Min KH, et al. Bone. 2022 Dec;165:116576. doi: 10.1016/j.bone.2022.116576. Epub 2022 Oct 3. Bone. 2022. PMID: 36195243 Review.
In addition, compromise of their development or resorbing machinery is pathogenic in multiple types of osteopetrosis. However, osteoclasts also have functions other than bone resorption. Like cells of the innate immune system, they are derived from myeloid precursors and r …
In addition, compromise of their development or resorbing machinery is pathogenic in multiple types of osteopetrosis. However, osteoc …
432 results