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1.
Three-way contact analysis characterizes the higher order organization of the Tcra locus.
Nucleic Acids Res
; 51(17): 8987-9000, 2023 09 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-37534534
2.
[Clinical features and genetic analysis of 17 Chinese pedigrees affected with X-linked intellectual disability].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 41(5): 533-539, 2024 May 10.
Artículo
en Zh
| MEDLINE | ID: mdl-38684296
3.
Risk factors and healing factors for pharyngocutaneous fistula after total laryngectomy for laryngeal cancer: An epidemiological study.
Int Wound J
; 21(4): e14706, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38660912
4.
Screening and identification of miR-181a-5p in oral squamous cell carcinoma and functional verification in vivo and in vitro.
BMC Cancer
; 23(1): 162, 2023 Feb 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-36800936
5.
A role of the CTCF binding site at enhancer Eα in the dynamic chromatin organization of the Tcra-Tcrd locus.
Nucleic Acids Res
; 48(17): 9621-9636, 2020 09 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-32853367
6.
The role of chromatin organizer Satb1 in shaping TCR repertoire in adult thymus.
Genome
; 64(9): 821-832, 2021 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-33617384
7.
[Identification of SPAST gene variant in a pedigree affected with hereditary spastic paraplegia type 4].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(11): 1261-1264, 2020 Nov 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33179235
8.
Long noncoding RNA SOX2-OT facilitates laryngeal squamous cell carcinoma development by epigenetically inhibiting PTEN via methyltransferase EZH2.
IUBMB Life
; 71(9): 1230-1239, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-30811870
9.
[Identification of two novel Parkin gene mutations in a patient affected with Juvenile Parkinson's syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(4): 344-347, 2019 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-30950022
10.
[Analysis of MYO7A gene mutation in a family with non-syndromic autosomal recessive deafness].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(10): 965-969, 2019 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31598937
11.
[Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(10): 1022-1024, 2019 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31598951
12.
A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss.
Hum Genet
; 137(6-7): 437-446, 2018 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-29860631
13.
Security and Sharing of NIPT Data Are the Basis of Ethical Decision-Making Related to Non-Medical Traits.
Am J Bioeth
; 23(3): 29-31, 2023 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36919545
14.
[Analysis of pathological mutation in a Chinese pedigree affected with familial exudative vitreoretinopathy].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(2): 193-196, 2018 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29652990
15.
[Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(1): 91-95, 2018 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29419870
16.
[Phenotypic and genetic analysis of a child carrying a 17q11.2 microdeletion].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(5): 695-698, 2017 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-28981936
17.
[Analysis of PRRT2 gene mutations in a Chinese family affected with paroxysmal kinesigenic dyskinesia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(1): 61-3, 2016 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-26829736
18.
[Phenotypic and genetic analysis of a child featuring multiple malformations due to chromosome 14q deletion].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 33(3): 361-4, 2016 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-27264822
19.
[Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 32(6): 823-6, 2015 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-26663057
20.
[Mutation analysis and prenatal diagnosis of COL1A1 gene in a Chinese family with type I osteogenesis imperfecta].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(6): 730-2, 2014 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-25449076