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1.
Rodents mediate the relationship between seed rain, seed bank, and plant community with increased grazing disturbance.
Ecol Appl
; : e2984, 2024 May 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-38753679
2.
Machine Learning-Based Perihematomal Tissue Features to Predict Clinical Outcome after Spontaneous Intracerebral Hemorrhage.
J Stroke Cerebrovasc Dis
; 31(6): 106475, 2022 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-35417846
3.
[Genetic analysis of PYGL gene variants for a child with Glycogen storage disease VI].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(2): 209-212, 2022 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-35076922
4.
De Novo ARID1B mutations cause growth delay associated with aberrant Wnt/ß-catenin signaling.
Hum Mutat
; 41(5): 1012-1024, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31981384
5.
Eosinophilic colitis in a boy with a novel XIAP mutation: a case report.
BMC Pediatr
; 20(1): 171, 2020 04 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-32305064
6.
Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study.
Cell Physiol Biochem
; 49(1): 295-305, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30138938
7.
Mutations in methionyl-tRNA synthetase gene in a Chinese family with interstitial lung and liver disease, postnatal growth failure and anemia.
J Hum Genet
; 62(6): 647-651, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28148924
8.
Further delineation of the phenotype of truncating KMT2A mutations: The extended Wiedemann-Steiner syndrome.
Am J Med Genet A
; 173(2): 510-514, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27759909
9.
Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis.
BMC Pediatr
; 14: 267, 2014 Oct 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25319636
10.
Diagnostic yield and novel candidate genes by next generation sequencing in 166 children with intrahepatic cholestasis.
Hepatol Int
; 18(2): 661-672, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-37314652
11.
Warming reduced flowering synchrony and extended community flowering season in an alpine meadow on the Tibetan Plateau.
Ecology
; 104(1): e3862, 2023 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36062319
12.
Antisense oligonucleotides rescue an intronic splicing variant in the ABCB11 gene that causes progressive familial intrahepatic cholestasis type 2.
Dig Liver Dis
; 54(11): 1541-1547, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35490150
13.
A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case Report.
Front Pediatr
; 8: 118, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32292771
14.
Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarray.
Mol Cytogenet
; 9: 16, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26884814
15.
Curcumin-induced histone acetylation inhibition improves stress-induced gastric ulcer disease in rats.
Mol Med Rep
; 11(3): 1911-6, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25405899
16.
Association between TGFB1 915G/C polymorphism and susceptibility to chronic hepatitis C virus infection: A meta-analysis.
Biomed Rep
; 2(2): 239-244, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24649103
17.
Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencing.
Mol Med Rep
; 10(3): 1264-74, 2014 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-24969679
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