Detalles de la búsqueda
1.
A Proline-Based Artificial Enzyme That Favors Aldol Condensation Enables Facile Synthesis of Aliphatic Ketones via Tandem Catalysis.
ACS Synth Biol;
13(4): 1100-1104, 2024 Apr 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-38587465
2.
Development and validation of a machine learning-based predictive model for assessing the 90-day prognostic outcome of patients with spontaneous intracerebral hemorrhage.
J Transl Med;
22(1): 236, 2024 Mar 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-38439097
3.
Characteristics analysis of solid waste generation and carbon emission of beer production in China.
Environ Res;
245: 118017, 2024 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38157965
4.
Efficacy of cecal retroflexion observed on adenoma missing of ascending colon during colonoscopy: A prospective, randomized, pilot trial.
Medicine (Baltimore);
102(34): e34806, 2023 Aug 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-37653767
5.
Re-recognition of BMPR1A-related polyposis: beyond juvenile polyposis and hereditary mixed polyposis syndrome.
Gastroenterol Rep (Oxf);
11: goac082, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36632626
6.
Effect of Anterograde Lavage via Temporary Loop Ileostoma on the Recovery of Bowel Function in Patients Receiving Stoma Closure: A Retrospective Cohort Study.
Dis Colon Rectum;
66(1): 148-154, 2023 01 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36515517
7.
Recurrent sigmoid volvulus relieved by transanal ileus tube implantation.
Gastroenterol Rep (Oxf);
10: goac030, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35785265
8.
Delayed diagnosis of Peutz-Jeghers syndrome due to pathological information loss or mistake in family/personal history.
Orphanet J Rare Dis;
16(1): 261, 2021 06 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34103092
9.
Colonoscopic diagnosis of rectal endometriosis without obvious or exact mucosa-infiltrated signs: A Video Vignette.
Colorectal Dis;
23(6): 1593-1594, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33751772
10.
Identify DNA-Binding Proteins Through the Extreme Gradient Boosting Algorithm.
Front Genet;
12: 821996, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35154264
11.
Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene.
BMC Gastroenterol;
19(1): 70, 2019 May 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31072341
12.
STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.
Cancer Genet;
230: 47-57, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30528796
13.
Adenoma miss rate determined by very shortly repeated colonoscopy: Retrospective analysis of data from a single tertiary medical center in China.
Medicine (Baltimore);
97(38): e12297, 2018 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-30235675
14.
The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome.
BMC Med Genet;
19(1): 141, 2018 08 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-30092773
15.
A novel STK11 missense mutation (c.346Gâ¯>â¯T) causing Peutz-Jeghers syndrome in a Chinese male with a negative family history.
Dig Liver Dis;
50(8): 864-866, 2018 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29921539
16.
Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.
BMC Surg;
18(1): 24, 2018 Apr 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-29685139
17.
A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family.
Dig Liver Dis;
50(3): 312-314, 2018 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-29301733
18.
Drugs for Neuropathic Pain Are Promising in Treating Feed-induced Dystonia in Central Nervous System Disabled Children.
J Pediatr Gastroenterol Nutr;
66(1): e25, 2018 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28902092
19.
A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.
Medicine (Baltimore);
96(49): e8591, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29245219
20.
Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.
BMC Med Genet;
18(1): 130, 2017 11 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29141581