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.
2. Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta. Cabral WA; Ishikawa M; Garten M; Makareeva EN; Sargent BM; Weis M; Barnes AM; Webb EA; Shaw NJ; Ala-Kokko L; Lacbawan FL; Högler W; Leikin S; Blank PS; Zimmerberg J; Eyre DR; Yamada Y; Marini JC PLoS Genet; 2016 Jul; 12(7):e1006156. PubMed ID: 27441836 [TBL] [Abstract][Full Text] [Related]
3. Mice lacking the intracellular cation channel TRIC-B have compromised collagen production and impaired bone mineralization. Zhao C; Ichimura A; Qian N; Iida T; Yamazaki D; Noma N; Asagiri M; Yamamoto K; Komazaki S; Sato C; Aoyama F; Sawaguchi A; Kakizawa S; Nishi M; Takeshima H Sci Signal; 2016 May; 9(428):ra49. PubMed ID: 27188440 [TBL] [Abstract][Full Text] [Related]
4. CaMKII inhibition due to TRIC-B loss-of-function dysregulates SMAD signaling in osteogenesis imperfecta. Besio R; Contento BM; Garibaldi N; Filibian M; Sonntag S; Shmerling D; Tonelli F; Biggiogera M; Brini M; Salmaso A; Jovanovic M; Marini JC; Rossi A; Forlino A Matrix Biol; 2023 Jun; 120():43-59. PubMed ID: 37178987 [TBL] [Abstract][Full Text] [Related]
5. A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta. Volodarsky M; Markus B; Cohen I; Staretz-Chacham O; Flusser H; Landau D; Shelef I; Langer Y; Birk OS Hum Mutat; 2013 Apr; 34(4):582-6. PubMed ID: 23316006 [TBL] [Abstract][Full Text] [Related]
6. Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta. Lv F; Xu XJ; Wang JY; Liu Y; Asan ; Wang JW; Song LJ; Song YW; Jiang Y; Wang O; Xia WB; Xing XP; Li M J Hum Genet; 2016 Jun; 61(6):539-45. PubMed ID: 26911354 [TBL] [Abstract][Full Text] [Related]
7. A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. Rubinato E; Morgan A; D'Eustacchio A; Pecile V; Gortani G; Gasparini P; Faletra F Gene; 2014 Jul; 545(2):290-2. PubMed ID: 24835313 [TBL] [Abstract][Full Text] [Related]
8. Zebrafish Tric-b is required for skeletal development and bone cells differentiation. Tonelli F; Leoni L; Daponte V; Gioia R; Cotti S; Fiedler IAK; Larianova D; Willaert A; Coucke PJ; Villani S; Busse B; Besio R; Rossi A; Witten PE; Forlino A Front Endocrinol (Lausanne); 2023; 14():1002914. PubMed ID: 36755921 [TBL] [Abstract][Full Text] [Related]
9. TRIC channels are essential for Ca2+ handling in intracellular stores. Yazawa M; Ferrante C; Feng J; Mio K; Ogura T; Zhang M; Lin PH; Pan Z; Komazaki S; Kato K; Nishi M; Zhao X; Weisleder N; Sato C; Ma J; Takeshima H Nature; 2007 Jul; 448(7149):78-82. PubMed ID: 17611541 [TBL] [Abstract][Full Text] [Related]
10. Absence of TRIC-B from type XIV Osteogenesis Imperfecta osteoblasts alters cell adhesion and mitochondrial function - A multi-omics study. Jovanovic M; Mitra A; Besio R; Contento BM; Wong KW; Derkyi A; To M; Forlino A; Dale RK; Marini JC Matrix Biol; 2023 Aug; 121():127-148. PubMed ID: 37348683 [TBL] [Abstract][Full Text] [Related]
11. Trimeric intracellular cation channels and sarcoplasmic/endoplasmic reticulum calcium homeostasis. Zhou X; Lin P; Yamazaki D; Park KH; Komazaki S; Chen SR; Takeshima H; Ma J Circ Res; 2014 Feb; 114(4):706-16. PubMed ID: 24526676 [TBL] [Abstract][Full Text] [Related]
12. Atypical cell death and insufficient matrix organization in long-bone growth plates from Tric-b-knockout mice. Ichimura A; Miyazaki Y; Nagatomo H; Kawabe T; Nakajima N; Kim GE; Tomizawa M; Okamoto N; Komazaki S; Kakizawa S; Nishi M; Takeshima H Cell Death Dis; 2023 Dec; 14(12):848. PubMed ID: 38123563 [TBL] [Abstract][Full Text] [Related]
13. Enhanced activity of multiple TRIC-B channels: an endoplasmic reticulum/sarcoplasmic reticulum mechanism to boost counterion currents. O'Brien F; Eberhardt D; Witschas K; El-Ajouz S; Iida T; Nishi M; Takeshima H; Sitsapesan R; Venturi E J Physiol; 2019 May; 597(10):2691-2705. PubMed ID: 30907436 [TBL] [Abstract][Full Text] [Related]
14. Knocking out TMEM38B in human foetal osteoblasts hFOB 1.19 by CRISPR/Cas9: A model for recessive OI type XIV. Leoni L; Tonelli F; Besio R; Gioia R; Moccia F; Rossi A; Forlino A PLoS One; 2021; 16(9):e0257254. PubMed ID: 34582479 [TBL] [Abstract][Full Text] [Related]