Detalhe da pesquisa
1.
Vision-based collective motion: A locust-inspired reductionist model.
PLoS Comput Biol
; 20(1): e1011796, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38285716
2.
Efficacy of dupilumab in real-life settings: a STROBE study.
Eur Arch Otorhinolaryngol
; 2024 Mar 18.
Artigo
Inglês
| MEDLINE | ID: mdl-38498194
3.
A multifunctional matching algorithm for sample design in agricultural plots.
Comput Electron Agric
; 187: None, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-34381288
4.
Precooling Strategy Allows Exponentially Faster Heating.
Phys Rev Lett
; 124(6): 060602, 2020 Feb 14.
Artigo
Inglês
| MEDLINE | ID: mdl-32109080
5.
Resolving the Λ Hypernuclear Overbinding Problem in Pionless Effective Field Theory.
Phys Rev Lett
; 121(10): 102502, 2018 Sep 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30240262
6.
Canine intrathoracic sarcoma with ultrastructural characteristics of human synovial sarcoma - case report.
BMC Vet Res
; 13(1): 247, 2017 Aug 16.
Artigo
Inglês
| MEDLINE | ID: mdl-28814294
7.
Three body calculation of the ΔΔ dibaryon candidate D(03)(2370).
Phys Rev Lett
; 111(17): 172301, 2013 Oct 25.
Artigo
Inglês
| MEDLINE | ID: mdl-24206479
8.
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness.
Nat Genet
; 7(1): 64-8, 1994 May.
Artigo
Inglês
| MEDLINE | ID: mdl-8075643
9.
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese.
Nat Genet
; 10(3): 360-2, 1995 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-7670478
10.
Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.
Nat Genet
; 2(2): 139-43, 1992 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-1303264
11.
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
Nat Genet
; 26(3): 270-1, 2000 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-11062461
12.
Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy.
Nat Genet
; 28(2): 123-4, 2001 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-11381255
13.
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation.
Nat Genet
; 26(2): 247-50, 2000 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-11017088
14.
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
Nat Genet
; 17(2): 194-7, 1997 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-9326941
15.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Nat Genet
; 26(1): 51-5, 2000 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-10973247
16.
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.
Nat Genet
; 22(3): 255-9, 1999 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-10391212
17.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Nat Genet
; 27(1): 108-12, 2001 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-11138009
18.
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
Nat Genet
; 26(3): 319-23, 2000 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-11062471
19.
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.
Nat Genet
; 27(1): 59-63, 2001 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-11137999
20.
The hybrid bio-robotic swarm as a powerful tool for collective motion research: a perspective.
Front Neurorobot
; 17: 1215085, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37520677