J H Duncan Bassett
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Explore the profile of J H Duncan Bassett including associated specialties, affiliations and a list of published articles.
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77
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3082
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Recent Articles
1.
Loisay L, Komla-Ebri D, Morice A, Heuze Y, Viaut C, de La Seigliere A, et al.
JCI Insight
. 2023 Jun;
8(12).
PMID: 37345656
Hypochondroplasia (HCH) is a mild dwarfism caused by missense mutations in fibroblast growth factor receptor 3 (FGFR3), with the majority of cases resulting from a heterozygous p.Asn540Lys gain-of-function mutation. Here,...
2.
Kooblall K, Stevenson M, Stewart M, Harris L, Zalucki O, Dewhurst H, et al.
JBMR Plus
. 2023 Jun;
7(6):e10739.
PMID: 37283649
The nuclear factor I/X () gene encodes a ubiquitously expressed transcription factor whose mutations lead to two allelic disorders characterized by developmental, skeletal, and neural abnormalities, namely, Malan syndrome (MAL)...
3.
Foessl I, Bassett J, Bjornerem A, Busse B, Calado A, Chavassieux P, et al.
Front Endocrinol (Lausanne)
. 2021 Dec;
12:720728.
PMID: 34925226
A synoptic overview of scientific methods applied in bone and associated research fields across species has yet to be published. Experts from the EU Cost Action GEMSTONE ("GEnomics of MusculoSkeletal...
4.
Lademann F, Mayerl S, Tsourdi E, Verrey F, Leitch V, Williams G, et al.
Endocrinology
. 2021 Oct;
163(1).
PMID: 34669927
Thyroid hormones (TH) are essential for skeletal development and adult bone homeostasis. Their bioavailability is determined by specific transporter proteins at the cell surface. The TH-specific transporter monocarboxylate transporter 8...
5.
Formosa M, Bergen D, Gregson C, Maurizi A, Kampe A, Garcia-Giralt N, et al.
Front Endocrinol (Lausanne)
. 2021 Sep;
12:709711.
PMID: 34539568
Genetic disorders of the skeleton encompass a diverse group of bone diseases differing in clinical characteristics, severity, incidence and molecular etiology. Of particular interest are the monogenic rare bone mass...
6.
Butterfield N, Curry K, Steinberg J, Dewhurst H, Komla-Ebri D, Mannan N, et al.
Nat Commun
. 2021 May;
12(1):3302.
PMID: 34050183
No abstract available.
7.
Youlten S, Kemp J, Logan J, Ghirardello E, Sergio C, Dack M, et al.
Nat Commun
. 2021 May;
12(1):2444.
PMID: 33953184
Osteocytes are master regulators of the skeleton. We mapped the transcriptome of osteocytes from different skeletal sites, across age and sexes in mice to reveal genes and molecular programs that...
8.
McDonald M, Khoo W, Ng P, Xiao Y, Zamerli J, Thatcher P, et al.
Cell
. 2021 Apr;
184(7):1940.
PMID: 33798441
No abstract available.
9.
Steinberg J, Southam L, Roumeliotis T, Clark M, Jayasuriya R, Swift D, et al.
Nat Commun
. 2021 Feb;
12(1):1309.
PMID: 33637762
Osteoarthritis causes pain and functional disability for over 500 million people worldwide. To develop disease-stratifying tools and modifying therapies, we need a better understanding of the molecular basis of the...
10.
McDonald M, Khoo W, Ng P, Xiao Y, Zamerli J, Thatcher P, et al.
Cell
. 2021 Feb;
184(5):1330-1347.e13.
PMID: 33636130
Osteoclasts are large multinucleated bone-resorbing cells formed by the fusion of monocyte/macrophage-derived precursors that are thought to undergo apoptosis once resorption is complete. Here, by intravital imaging, we reveal that...