Detalhe da pesquisa
1.
Immunity and lifespan: answering long-standing questions with comparative genomics.
Trends Genet
; 38(7): 650-661, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35469708
2.
Understanding the evolution of immune genes in jawed vertebrates.
J Evol Biol
; 36(6): 847-873, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37255207
3.
Clinical practice guidelines for the antenatal management of dichorionic diamniotic twin pregnancies: a systematic review.
BMC Pregnancy Childbirth
; 23(1): 347, 2023 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37179347
4.
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.
Acta Neuropathol
; 144(4): 707-731, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35948834
5.
INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH.
Brain
; 144(8): 2427-2442, 2021 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33792664
6.
Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome.
Hum Mol Genet
; 28(14): 2339-2351, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31220253
7.
MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion.
Hum Mol Genet
; 27(8): 1434-1446, 2018 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29462312
8.
Wetter climates select for higher immune gene diversity in resident, but not migratory, songbirds.
Proc Biol Sci
; 287(1919): 20192675, 2020 01 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31992169
9.
SIL1 deficiency causes degenerative changes of peripheral nerves and neuromuscular junctions in fish, mice and human.
Neurobiol Dis
; 124: 218-229, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30468864
10.
Sympathetic innervation controls homeostasis of neuromuscular junctions in health and disease.
Proc Natl Acad Sci U S A
; 113(3): 746-50, 2016 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-26733679
11.
Extreme MHC class I diversity in the sedge warbler (Acrocephalus schoenobaenus); selection patterns and allelic divergence suggest that different genes have different functions.
BMC Evol Biol
; 17(1): 159, 2017 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28679358
12.
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome.
Brain
; 139(Pt 8): 2143-53, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27259756
13.
Organizational factors to optimize mental health nurses' wellbeing in the workplace: An integrative literature review.
Int J Ment Health Nurs
; 33(1): 5-17, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37650491
14.
A systematic review of standardised tools used in perinatal death review programmes.
Women Birth
; 37(1): 88-97, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37793961
15.
Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes.
Nat Commun
; 15(1): 1227, 2024 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38418480
16.
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.
Nat Commun
; 14(1): 1009, 2023 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36823193
17.
A protocol for a systematic review of standardised tools used in perinatal death review programmes.
HRB Open Res
; 5: 52, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-37753168
18.
Retrospective national cohort study of pregnancy outcomes for women with type 1 and type 2 diabetes mellitus in Republic of Ireland.
Diabetes Res Clin Pract
; 189: 109947, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35709911
19.
Trade-offs in expressed major histocompatibility complex diversity seen on a macroevolutionary scale among songbirds.
Evolution
; 75(5): 1061-1069, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33666228
20.
Living with relatives offsets the harm caused by pathogens in natural populations.
Elife
; 102021 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34309511