Found: 17
Select item for more details and to access through your institution.
3D printing-assisted preoperative plan of pedicle screw placement for middle-upper thoracic trauma: a cohort study.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Improved paclitaxel accumulation in cell suspension cultures of Taxus chinensis by brassinolide.
- Published in:
- Biotechnology Letters, 2001, v. 23, n. 13, p. 1047, doi. 10.1023/A:1010589304749
- By:
- Publication type:
- Article
A genome-wide CRISPR-Cas9 knockout screen identifies FSP1 as the warfarin-resistant vitamin K reductase.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36446-8
- By:
- Publication type:
- Article
Identification and characterization of a special type of subnuclear structure: AGGF1‐coated paraspeckles.
- Published in:
- FASEB Journal, 2022, v. 36, n. 6, p. 1, doi. 10.1096/fj.202101690RR
- By:
- Publication type:
- Article
Four conserved cysteines of VKORC1L1 function in concert in the vitamin K cycle (739.1).
- Published in:
- FASEB Journal, 2014, v. 28, p. N.PAG, doi. 10.1096/fasebj.28.1_supplement.739.1
- By:
- Publication type:
- Article
Naturally occurring UBIAD1 mutations differentially affect menaquinone biosynthesis and vitamin K‐dependent carboxylation.
- Published in:
- FEBS Journal, 2022, v. 289, n. 9, p. 2613, doi. 10.1111/febs.16291
- By:
- Publication type:
- Article
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 11, p. 660, doi. 10.1038/jhg.2009.92
- By:
- Publication type:
- Article
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1133, doi. 10.1007/s10038-006-0071-8
- By:
- Publication type:
- Article
Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm.
- Published in:
- BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0310-6
- By:
- Publication type:
- Article
A genome‐wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertension.
- Published in:
- Clinical & Translational Medicine, 2021, v. 11, n. 5, p. 1, doi. 10.1002/ctm2.388
- By:
- Publication type:
- Article
Danshensu inhibits the IL-1β-induced inflammatory response in chondrocytes and osteoarthritis possibly via suppressing NF-κB signaling pathway.
- Published in:
- Molecular Medicine, 2021, v. 27, n. 1, p. 1, doi. 10.1186/s10020-021-00329-9
- By:
- Publication type:
- Article
NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling.
- Published in:
- Obesity (19307381), 2023, v. 31, n. 1, p. 123, doi. 10.1002/oby.23580
- By:
- Publication type:
- Article
Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang–Wang syndrome.
- Published in:
- Acta Physiologica, 2022, v. 235, n. 1, p. 1, doi. 10.1111/apha.13800
- By:
- Publication type:
- Article
Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5‐cryab‐hspb2 signalling in zebrafish.
- Published in:
- Acta Physiologica, 2021, v. 231, n. 3, p. 1, doi. 10.1111/apha.13567
- By:
- Publication type:
- Article
Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation.
- Published in:
- Human Mutation, 2019, v. 40, n. 3, p. 310, doi. 10.1002/humu.23691
- By:
- Publication type:
- Article
NovelCACNA1Smutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 3, p. 203, doi. 10.1007/s00109-005-0638-4
- By:
- Publication type:
- Article
Inhibition of the NMDA receptor protects the rat sciatic nerve against ischemia/reperfusion injury.
- Published in:
- Experimental & Therapeutic Medicine, 2016, v. 11, n. 5, p. 1563, doi. 10.3892/etm.2016.3148
- By:
- Publication type:
- Article