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1.
The roles of transmembrane family proteins in the regulation of store-operated Ca2+ entry.
Cell Mol Life Sci
; 79(2): 118, 2022 Feb 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35119538
2.
Circular RNA hsa_circ_0081343 promotes trophoblast cell migration and invasion and inhibits trophoblast apoptosis by regulating miR-210-5p/DLX3 axis.
Reprod Biol Endocrinol
; 19(1): 123, 2021 Aug 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34365964
3.
TRIM59 promotes breast cancer motility by suppressing p62-selective autophagic degradation of PDCD10.
PLoS Biol
; 16(11): e3000051, 2018 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30408026
4.
Breakpoints Identification of a Balanced Complex Chromosome Rearrangement Case: 46,XX, t(6;15;10;9)(q13;q15;p11.2;q34.3) ins(9;8)(q22.33;q21.1q21.3).
Clin Lab
; 67(4)2021 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33865258
5.
There is a Strong Association between Early Preeclampsia and Congenital Heart Defects: A Large Population-Based, Retrospective Study.
Gynecol Obstet Invest
; 86(1-2): 40-47, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33341795
6.
[Clinical characterization and genetic analysis of a newborn with chromosome 8q21.11 deletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(2): 145-149, 2021 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33565068
7.
[Genetic analysis of a family with congenital heart defects caused by chromosome 8p23.1 deletion].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(1): 44-47, 2020 Jan 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31922595
8.
[46,XY DSD induced by a novel mutation c.458T>C (p.Leu153Pro) of the LHCGR gene: A case report and review of the literature].
Zhonghua Nan Ke Xue
; 26(12): 1105-1111, 2020 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-34898086
9.
Single-Cell Sequencing Reveals the Relationship between Phenotypes and Genotypes of Klinefelter Syndrome.
Cytogenet Genome Res
; 159(2): 55-65, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31630146
10.
Compound heterozygous variants in MYH11 underlie autosomal recessive megacystis-microcolon-intestinal hypoperistalsis syndrome in a Chinese family.
J Hum Genet
; 64(11): 1067-1073, 2019 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-31427716
11.
Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissue.
J Assist Reprod Genet
; 36(12): 2525-2531, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31720905
12.
De Novo Mutated TUBB2B Associated Pachygyria Diagnosed by Medical Exome Sequencing and Long-Range PCR.
Fetal Pediatr Pathol
; 38(1): 63-71, 2019 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-30585108
13.
A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report.
BMC Med Genet
; 19(1): 193, 2018 11 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30400883
14.
[Genetic analysis and prenatal diagnosis for ten families affected with tuberous sclerosis complex].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(1): 18-22, 2018 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-29419853
15.
UPD16 itself is not a cause of intrauterine growth restriction.
Fetal Pediatr Pathol
; 37(6): 452-464, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-30468402
16.
Evidence That Does Not Support Pyruvate Kinase M2 (PKM2)-catalyzed Reaction as a Rate-limiting Step in Cancer Cell Glycolysis.
J Biol Chem
; 291(17): 8987-99, 2016 Apr 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-26917721
17.
The significance of polymorphism and expression of oestrogen metabolism-related genes in Chinese women with premature ovarian insufficiency.
Reprod Biomed Online
; 35(5): 609-615, 2017 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-28887105
18.
Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy.
Clin Chem Lab Med
; 55(3): 358-367, 2017 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27754957
19.
A Novel Case of 15q24 Microdeletion Syndrome Detected by MLPA in a Chinese Family.
Clin Lab
; 63(9): 1501-1506, 2017 Sep 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28879703
20.
[Analysis of a mistake occurring during prenatal diagnosis of two couples respectively carrying CD41-42 (-TCTT) and CD43(G>T) mutations of the beta hemoglobin gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(5): 684-687, 2017 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-28981933