Detalhe da pesquisa
1.
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
Cell
; 140(1): 74-87, 2010 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-20074521
2.
Overall and central obesity and prostate cancer risk in African men.
Cancer Causes Control
; 33(2): 223-239, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34783926
3.
Anticoagulant profile of subcutaneous enoxaparin in healthy dogs.
J Vet Pharmacol Ther
; 45(1): 34-45, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34622463
4.
Harmonizing research outcomes for polycystic ovary syndrome (HARP), a marathon not a sprint: current challenges and future research need.
Hum Reprod
; 36(3): 523-528, 2021 02 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33332572
5.
Multiphase Assembly of Small Molecule Microcrystalline Peptide Hydrogel Allows Immunomodulatory Combination Therapy for Long-Term Heart Transplant Survival.
Small
; 16(38): e2002791, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32812339
6.
Harmonising research outcomes for polycystic ovary syndrome: an international multi-stakeholder core outcome set.
Hum Reprod
; 35(2): 404-412, 2020 02 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32020203
7.
Plasma and synovial fluid pharmacokinetics of a single intravenous dose of meropenem in adult horses.
J Vet Pharmacol Ther
; 42(5): 525-529, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31222751
8.
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development.
Am J Med Genet A
; 170A(2): 297-305, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26639658
9.
Generation of a de novo transcriptome from equine lamellar tissue.
BMC Genomics
; 16: 739, 2015 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26432030
10.
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.
Am J Hum Genet
; 91(1): 171-9, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22770981
11.
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.
Hum Mol Genet
; 21(26): 5484-99, 2012 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23001566
12.
Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome.
Ophthalmology
; 121(7): 1461-8, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24612975
13.
A novel syndrome caused by the E410K amino acid substitution in the neuronal ß-tubulin isotype 3.
Brain
; 136(Pt 2): 522-35, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23378218
14.
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.
Nat Genet
; 37(10): 1035-7, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16155570
15.
The Impact of COVID-19 on Breastfeeding Initiation and Duration in a Low-Income Population, Washington, DC.
Breastfeed Med
; 19(2): 120-128, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38386992
16.
Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men.
bioRxiv
; 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38293167
17.
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
medRxiv
; 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38585811
18.
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
Nat Genet
; 35(4): 318-21, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14595441
19.
The Agent Preference in Visual Event Apprehension.
Open Mind (Camb)
; 7: 240-282, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37416075
20.
IL-27 induces an IFN-like signature in murine macrophages which in turn modulate colonic epithelium.
Front Immunol
; 14: 1021824, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37153622