Detalhe da pesquisa
1.
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.
Am J Respir Crit Care Med
; 2024 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38626355
2.
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
Am J Hum Genet
; 105(5): 1030-1039, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31630787
3.
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.
Am J Hum Genet
; 103(6): 995-1008, 2018 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30471718
4.
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms.
Am J Hum Genet
; 102(5): 973-984, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29727693
5.
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system.
Mol Hum Reprod
; 27(3)2021 02 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33561200
6.
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.
PLoS Genet
; 14(8): e1007602, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30148830
7.
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects.
Am J Hum Genet
; 100(1): 160-168, 2017 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28041644
8.
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization.
Am J Hum Genet
; 99(2): 460-9, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486780
9.
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex.
Am J Hum Genet
; 97(4): 546-54, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26387594
10.
The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin.
Development
; 142(1): 174-84, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25516973
11.
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect.
Hum Mutat
; 38(8): 964-969, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28543983
12.
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.
Am J Hum Genet
; 95(3): 257-74, 2014 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25192045
13.
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis.
Hum Mutat
; 37(4): 396-405, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26777464
14.
DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes.
Am J Respir Cell Mol Biol
; 55(2): 213-24, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26909801
15.
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry.
Am J Hum Genet
; 93(2): 357-67, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23849778
16.
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.
Am J Hum Genet
; 93(4): 711-20, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24055112
17.
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.
Am J Hum Genet
; 93(4): 672-86, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24094744
18.
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.
Am J Hum Genet
; 93(2): 336-45, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23891469
19.
The BEAT-PCD (Better Experimental Approaches to Treat Primary Ciliary Dyskinesia) Clinical Research Collaboration.
Eur Respir J
; 57(2)2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33541936
20.
Immunofluorescence Analysis and Diagnosis of Primary Ciliary Dyskinesia with Radial Spoke Defects.
Am J Respir Cell Mol Biol
; 53(4): 563-73, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25789548