Detalles de la búsqueda
1.
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.
Am J Hum Genet
; 105(4): 803-812, 2019 10 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31564438
2.
Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms.
J Med Genet
; 58(7): 465-474, 2021 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32737134
3.
Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss.
Neural Plast
; 2020: 6137083, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32684921
4.
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation.
Neural Plast
; 2020: 8841522, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32802038
5.
[Permeation mechanism of phenolic acid components from traditional Chinese medicine on PES membrane separation process].
Zhongguo Zhong Yao Za Zhi
; 45(1): 106-112, 2020 Jan.
Artículo
en Zh
| MEDLINE | ID: mdl-32237418
6.
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.
J Med Genet
; 55(5): 298-306, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29453195
7.
Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.
BMC Med Genet
; 19(1): 157, 2018 09 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30176854
8.
[Preliminary study on RC membrane permeability and mechanism of seven traditional Chinese medicine alkaloids such as berberine].
Zhongguo Zhong Yao Za Zhi
; 43(19): 3876-3883, 2018 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-30453712
9.
Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.
Neural Plast
; 2017: 3192090, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28695016
10.
Progress in studies of the mechanisms and clinical diagnosis of cervical carcinoma associated with genomic integration of high-risk human papillomavirus DNA.
Yi Chuan
; 39(9): 775-783, 2017 Sep 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-28936976
11.
Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss.
Am J Med Genet A
; 167A(10): 2357-65, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26079994
12.
Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families.
Heliyon
; 10(6): e27041, 2024 Mar 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-38501023
13.
MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.
BMC Med Genomics
; 17(1): 32, 2024 Jan 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-38254107
14.
Radiating blood flow signal: A new ultrasound feature of thyroid carcinoma.
Eur J Radiol
; 176: 111502, 2024 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-38759544
15.
Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing.
J Transl Med
; 11: 284, 2013 Nov 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-24206587
16.
[Pollution Characterizations and Oxidative Potentials of Water-Soluble Organic Matters at Different Polarity Levels in Winter PM2.5 Over Xi'an].
Huan Jing Ke Xue
; 44(4): 1882-1889, 2023 Apr 08.
Artículo
en Zh
| MEDLINE | ID: mdl-37040939
17.
[Clinical observation of virtual reality technology combined with isokinetic strength training for patients after anterior cruciate ligament reconstruction].
Zhongguo Gu Shang
; 36(12): 1159-64, 2023 Dec 25.
Artículo
en Zh
| MEDLINE | ID: mdl-38130225
18.
Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling.
J Transl Med
; 10: 225, 2012 Nov 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-23151025
19.
Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss.
Front Genet
; 13: 825082, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35711932
20.
Transcriptome analysis of the early stage ifnlr1-mutant zebrafish indicates the immune response to auditory dysfunction.
Gene Expr Patterns
; 43: 119229, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34968768