Detalhe da pesquisa
1.
Mutant p53 Gains Its Function via c-Myc Activation upon CDK4 Phosphorylation at Serine 249 and Consequent PIN1 Binding.
Mol Cell
; 68(6): 1134-1146.e6, 2017 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29225033
2.
RPS: a comprehensive database of RNAs involved in liquid-liquid phase separation.
Nucleic Acids Res
; 50(D1): D347-D355, 2022 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34718734
3.
TIRSF: a web server for screening gene signatures to predict Tumor immunotherapy response.
Nucleic Acids Res
; 50(W1): W761-W767, 2022 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35554556
4.
Cytogenomic aberrations in isolated multicystic dysplastic kidney in children.
Pediatr Res
; 91(3): 659-664, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33790410
5.
[Experience and lessons on guiding and governing clinical applications of chromosome microarray analysis in the United States].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(5): 419-424, 2021 May 10.
Artigo
em Zh
| MEDLINE | ID: mdl-33974247
6.
The Effects of Prosthesis Inversion/Eversion Stiffness on Balance-Related Variability During Level Walking: A Pilot Study.
J Biomech Eng
; 142(9)2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32280955
7.
[Recommendation for standardized certification of the directors of genetic diagnostics laboratories].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(1): 32-36, 2019 Jan 10.
Artigo
em Zh
| MEDLINE | ID: mdl-30722090
8.
TSCRE: a comprehensive database for tumor-specific cis-regulatory elements.
NAR Cancer
; 6(1): zcad063, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38213995
9.
Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
Am J Med Genet A
; 158A(9): 2139-51, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22847869
10.
Inspecting the Running Process of Horizontal Federated Learning via Visual Analytics.
IEEE Trans Vis Comput Graph
; 28(12): 4085-4100, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33872152
11.
Co-designing hardware and control for robot hands.
Sci Robot
; 6(54)2021 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34043541
12.
RAPID: A Rep-Seq Dataset Analysis Platform With an Integrated Antibody Database.
Front Immunol
; 12: 717496, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34484220
13.
Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations.
Behav Brain Funct
; 4: 20, 2008 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-18445268
14.
The complete chloroplast genome of monotypic fern, Mesopteris tonkinensis (Thelypteridaceae).
Mitochondrial DNA B Resour
; 3(2): 868-869, 2018 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33474348
15.
Preimplantation Genetic Screening with Spent Culture Medium/Blastocoel Fluid for in Vitro Fertilization.
Sci Rep
; 8(1): 9275, 2018 06 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29915225
16.
Molecular analysis of mitochondrial DNA point mutations by polymerase chain reaction.
Methods Mol Biol
; 336: 135-43, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16916259
17.
Development of a molecular screening test for hereditary hearing loss and genetic susceptibility to aminoglycoside toxicity for Chinese population.
Beijing Da Xue Xue Bao Yi Xue Ban
; 37(1): 51-4, 2005 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-15719042
18.
Constitutional mosaic trisomy 21 and azoospermia: a case report.
Beijing Da Xue Xue Bao Yi Xue Ban
; 37(1): 94-5, 2005 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-15719052
19.
Genomic and Clinicopathologic Features of Primary Myelofibrosis With Isolated 13q Deletion.
Clin Lymphoma Myeloma Leuk
; 15(8): 496-505.e1-2, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26027540
20.
Duplication at Xq28 involving IKBKG is associated with progressive macrocephaly, recurrent infections, ectodermal dysplasia, benign tumors, and neuropathy.
Clin Dysmorphol
; 23(3): 77-82, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24721901