Detalles de la búsqueda
1.
High light triggers flavonoid and polysaccharide synthesis through DoHY5-dependent signaling in Dendrobium officinale.
Plant J
; 115(4): 1114-1133, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37177908
2.
PLD2 deficiency alleviates endothelial glycocalyx degradation in LPS-induced ARDS/ALI.
Biochem Biophys Res Commun
; 716: 150019, 2024 Jul 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-38703555
3.
Regulation of carbohydrate metabolism during anther development in a thermo-sensitive genic male-sterile wheat line.
Plant Cell Environ
; 2024 Mar 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-38517937
4.
The prognostic value of age-adjusted Charlson comorbidity index in laparoscopic resection for hilar cholangiocarcinoma.
Scand J Gastroenterol
; 59(3): 333-343, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38018772
5.
Result of a Pilot External Quality Assessment Scheme for Clinical Diagnosis of Inherited Metabolic Disorders in China.
Clin Lab
; 70(4)2024 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38623669
6.
Persistence of severe global inequalities in the burden of Hypertension Heart Disease from 1990 to 2019: findings from the global burden of disease study 2019.
BMC Public Health
; 24(1): 110, 2024 01 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-38184560
7.
A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review.
BMC Pediatr
; 24(1): 104, 2024 Feb 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-38341530
8.
Association between estimated pulse wave velocity and in-hospital mortality of patients with acute kidney injury: a retrospective cohort analysis of the MIMIC-IV database.
Ren Fail
; 46(1): 2313172, 2024 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-38357758
9.
[Clinical and genetic analysis of two children with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(2): 199-204, 2024 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-38311559
10.
[Clinical phenotype and genetic characteristics of a Chinese pedigree affected with Spastic paraplegia type 5A].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(4): 437-442, 2024 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-38565509
11.
[Clinical features and genetic analysis of three children with ß-ketothiolase deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(3): 289-293, 2024 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-38448016
12.
A de novo low-frequency mosaic variant of KIF1A causes hereditary spastic paraplegia: A literature review.
Ann Hum Genet
; 87(4): 158-165, 2023 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36896784
13.
Wall-associated kinase GhWAK13 mediates arbuscular mycorrhizal symbiosis and Verticillium wilt resistance in cotton.
New Phytol
; 2023 Dec 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-38095050
14.
Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh-like syndrome with severe complex I deficiency.
J Hum Genet
; 68(4): 239-246, 2023 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-36482121
15.
Fine mapping and cloning of a novel BrSCC1 gene for seed coat color in Brassica rapa L.
Theor Appl Genet
; 136(1): 11, 2023 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-36658295
16.
Atomically dispersed Au anchored on CeO2to enhancing the antioxidant activity.
Nanotechnology
; 34(28)2023 Apr 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37114843
17.
Partial trisomy 9p and partial monosomy 7p of an infant inherited from maternal balanced translocation: a case report.
BMC Pediatr
; 23(1): 168, 2023 04 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-37046298
18.
Overexpression of chaperones GroEL/ES from Escherichia coli enhances indigo biotransformation production of cytochrome P450 BM3 mutant.
Biotechnol Lett
; 45(8): 993-1000, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37243776
19.
[Genetic analysis of a case with 11ß hydroxylase deficiency caused by CYP11B2/CYP11B1 chimeric gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(4): 462-467, 2023 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36972943
20.
[Clinical and genetic analysis of five children with Catecholaminergic polymorphic ventricular tachycardia due to variants of RYR2 gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(8): 960-965, 2023 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-37532495