Detalles de la búsqueda
1.
Paeoniae radix rubra:A review of ethnopharmacology, phytochemistry, pharmacological activities, therapeutic mechanism for blood stasis syndrome, and quality control.
Chem Biodivers
; : e202401119, 2024 Jun 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-38850115
2.
A novel mutation of KCNJ1 identified in an affected child with nephrolithiasis.
BMC Nephrol
; 23(1): 227, 2022 06 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-35761198
3.
[Prenatal diagnosis and genetic counselling for a pedigree carrying a large fragment deletion of 13q].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(3): 334-337, 2022 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-35315048
4.
[The phenotypes and genotypes of four patients with Dubin-Johnson syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(10): 1065-1069, 2022 Oct 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36184084
5.
[Ultrasonographic manifestation and genetic analysis of a fetus with nephronophthisis type 2].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(5): 559-562, 2020 May 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32335886
6.
[Clinical phenotype and genetic analysis of three pedigrees with 17q12 microdeletion syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(4): 397-400, 2020 Apr 10.
Artículo
en Zh
| MEDLINE | ID: mdl-32219821
7.
[Phenotype and genetic analysis of a pedigree affected with progressive familial intrahepatic cholestasis].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(8): 789-793, 2019 Aug 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31400129
8.
[Phenotype and genetic analysis of three patients with PKHD1 associated autosomal recessive polycystic kidney disease at childhood, teenage and advanced age].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(12): 1153-1157, 2019 Dec 10.
Artículo
en Zh
| MEDLINE | ID: mdl-31813136
9.
Up-regulated NRIP2 in colorectal cancer initiating cells modulates the Wnt pathway by targeting RORß.
Mol Cancer
; 16(1): 20, 2017 01 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-28137278
10.
Exploring the mechanism of Tingli Pill in the treatment of HFpEF based on network pharmacology and molecular docking.
Medicine (Baltimore)
; 103(16): e37727, 2024 Apr 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-38640300
11.
Compound heterozygous mutation of the SNX14 gene causes autosomal recessive spinocerebellar ataxia 20.
Front Genet
; 15: 1379366, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38655056
12.
Identification of chromosomal abnormalities in miscarriages by CNV-Seq.
Mol Cytogenet
; 17(1): 4, 2024 Feb 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-38369498
13.
Fecal metabolomics combined with 16S rRNA gene sequencing to analyze the effect of Jiaotai pill intervention in type 2 diabetes mellitus rats.
Front Nutr
; 10: 1135343, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37229468
14.
ANKRD22 is involved in the progression of prostate cancer.
Oncol Lett
; 18(4): 4106-4113, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31516611
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