Detalhe da pesquisa
1.
Missense mutations in PIEZO1, which encodes the Piezo1 mechanosensor protein, define Er red blood cell antigens.
Blood
; 141(2): 135-146, 2023 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36122374
2.
A systematic review of change in symptoms, well-being and quality of life with group singing in people with cancer and their caregivers.
Support Care Cancer
; 32(4): 246, 2024 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38520544
3.
Barriers and facilitators to implementing self-directed therapy activities in inpatient rehabilitation settings.
Aust Occup Ther J
; 70(5): 617-626, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37291993
4.
Feasibility of increasing the dosage of inpatient occupational therapy and physiotherapy rehabilitation via independent tasks and exercises: 'My Therapy'.
Aust Occup Ther J
; 66(6): 739-752, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31602693
5.
The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.
Transfusion
; 54(11): 2931-40, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24894016
6.
Is Next Generation Sequencing the future of blood group testing?
Transfus Apher Sci
; 50(2): 183-8, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24667159
7.
The Perceptions of Telehealth Physiotherapy for People with Bronchiectasis during a Global Pandemic-A Qualitative Study.
J Clin Med
; 11(5)2022 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35268406
8.
RhD variant caused by an in-frame triplet duplication in the RHD gene.
Transfusion
; 51(3): 570-3, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20738827
9.
Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype.
Nat Commun
; 11(1): 3569, 2020 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32678083
10.
The McLeod syndrome without acanthocytes.
Parkinsonism Relat Disord
; 14(4): 364-6, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-17870653
11.
Resistance to malaria through structural variation of red blood cell invasion receptors.
Science
; 356(6343)2017 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28522690
12.
McLeod syndrome: life-long neuropsychiatric disorder due to a novel mutation of the XK gene.
Psychiatr Genet
; 15(4): 291-3, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16314760
13.
Two missense mutations in the CD44 gene encode two new antigens of the Indian blood group system.
Transfusion
; 47(7): 1306-11, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17581168
14.
Patient interleukin-18 GCG haplotype associates with improved survival and decreased transplant-related mortality after unrelated-donor bone marrow transplantation.
Br J Haematol
; 126(5): 704-10, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15327523