Detalhe da pesquisa
1.
Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.
Hum Mol Genet
; 32(10): 1730-1740, 2023 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36708031
2.
The Gß-like protein Bcgbl1 regulates development and pathogenicity of the gray mold Botrytis cinerea via modulating two MAP kinase signaling pathways.
PLoS Pathog
; 19(12): e1011839, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38048363
3.
Knockdown of CCM3 promotes angiogenesis through activation and nuclear translocation of YAP/TAZ.
Biochem Biophys Res Commun
; 701: 149525, 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38320423
4.
Characterization of the gut microbiota in polycystic ovary syndrome with dyslipidemia.
BMC Microbiol
; 24(1): 169, 2024 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38760705
5.
Synthesis and Characterization of a Novel PET Tracer for Noninvasive Evaluation of FGL1 Status in Tumors.
Mol Pharm
; 2024 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38836286
6.
Predictive value of bronchoscopy combined with CT score for refractory mycoplasma pneumoniae pneumonia in children.
BMC Pulm Med
; 24(1): 251, 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38778338
7.
Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice.
Am J Hum Genet
; 107(3): 514-526, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32791035
8.
Recent Advances in Bioorthogonal Click Chemistry for Enhanced PET and SPECT Radiochemistry.
Bioconjug Chem
; 34(3): 457-476, 2023 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36811499
9.
ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.
Hum Reprod
; 38(6): 1213-1223, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37004249
10.
Comparison of bone microstructure and strength in the distal radius and tibia between the different types of primary hypertrophic osteoarthropathy: an HR-pQCT study.
Osteoporos Int
; 34(8): 1453-1464, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37202541
11.
Oncogene-targeting nanoprobes for early imaging detection of tumor.
J Nanobiotechnology
; 21(1): 197, 2023 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37340418
12.
Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos.
J Assist Reprod Genet
; 40(7): 1689-1702, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36864181
13.
Selectivity Control in the Direct CO Esterification over Pd@UiO-66: The Pd Location Matters.
Angew Chem Int Ed Engl
; 62(48): e202311625, 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37656120
14.
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.
Hum Mutat
; 43(3): 434-443, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34923715
15.
Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
Hum Genet
; 141(11): 1795-1809, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35587281
16.
A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
Clin Genet
; 101(1): 55-64, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34595750
17.
Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human.
Clin Genet
; 102(2): 130-135, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35543642
18.
Feasibility of in vivo CAR T cells tracking using streptavidin-biotin-paired positron emission tomography.
Eur J Nucl Med Mol Imaging
; 49(13): 4419-4426, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35902411
19.
Characterization in nonhuman primates of (R)-[18F]OF-Me-NB1 and (S)-[18F]OF-Me-NB1 for imaging the GluN2B subunits of the NMDA receptor.
Eur J Nucl Med Mol Imaging
; 49(7): 2153-2162, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35107627
20.
Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.
Reprod Biol Endocrinol
; 20(1): 5, 2022 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34980136