Detalles de la búsqueda
1.
All-silicon polarization-independent broadband achromatic metalens designed for the mid-wave and long-wave infrared.
Opt Express
; 31(26): 44340-44352, 2023 Dec 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-38178507
2.
Directional regulation and mechanism analysis of the surface properties of hydrothermal carbon by circulating liquid in the hydrothermal carbonization procedure.
Environ Res
; 229: 116003, 2023 07 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-37127106
3.
Snow Depth Estimation on Slopes Using GPS-Interferometric Reflectometry.
Sensors (Basel)
; 19(22)2019 Nov 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-31744110
4.
Improving GNSS Ambiguity Acceptance Test Performance with the Generalized Difference Test Approach.
Sensors (Basel)
; 18(9)2018 Sep 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-30205625
5.
The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencing.
Genet Med
; 19(8): 936-944, 2017 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28125085
6.
Rapid molecular diagnostics of severe primary immunodeficiency determined by using targeted next-generation sequencing.
J Allergy Clin Immunol
; 138(4): 1142-1151.e2, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27484032
7.
Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types.
Genet Med
; 18(5): 513-21, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26402642
8.
Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism.
Mol Genet Metab
; 117(3): 363-8, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26827111
9.
Next generation sequencing of patients with mut methylmalonic aciduria: Validation of somatic cell studies and identification of 16 novel mutations.
Mol Genet Metab
; 118(4): 264-71, 2016 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27233228
10.
Improved molecular diagnosis by the detection of exonic deletions with target gene capture and deep sequencing.
Genet Med
; 17(2): 99-107, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25032985
11.
[Changes of centrosome and related protein in malignant transformation of BEAS-2B cell induced by coal tar pitch smoke extracts].
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi
; 31(9): 661-6, 2013 Sep.
Artículo
en Zh
| MEDLINE | ID: mdl-24064120
12.
Corrigendum to "Next generation sequencing of patients with mut methylmalonic aciduria: Validation of somatic cell studies and identification of 16 novel mutations." [Mol. Genet. Metab. (Aug 2016); 118(4): 264-71].
Mol Genet Metab
; 120(3): 295, 2017 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28284539
13.
High-efficiency synthesis of Cu superfine particles via reducing cuprous and cupric oxides with monoethanolamine and their antimicrobial potentials.
J Colloid Interface Sci
; 608(Pt 1): 749-757, 2022 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-34634547
14.
The Cdc42-interacting protein-4 (CIP4) gene knock-out mouse reveals delayed and decreased endocytosis.
J Biol Chem
; 285(7): 4348-54, 2010 Feb 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-19920150
15.
A rational approach to tuning the pKa values of rhodamines for living cell fluorescence imaging.
Org Biomol Chem
; 9(6): 1723-6, 2011 Mar 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-21258698
16.
[Construction of lentiviral mediated CyPA siRNA and its functions in non-small cell lung cancer].
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi
; 28(2): 87-91, 2010 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-20450794
17.
A sensitive and selective fluorescent thiol probe in water based on the conjugate 1,4-addition of thiols to alpha,beta-unsaturated ketones.
Chemistry
; 15(20): 5096-103, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-19343759
18.
High-performance all-optical OR/NOR logic gate in a single semiconductor optical amplifier with delay interference filtering.
Appl Opt
; 48(14): 2638-41, 2009 May 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-19424383
19.
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
Genome Med
; 11(1): 48, 2019 07 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-31349857
20.
Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Nat Med
; 25(4): 701-702, 2019 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-30787481