Pesquisas alternativas:
bennett bruce » bennetts bruce (Expandir a Pesquisa), burnett bruce (Expandir a Pesquisa), bennett brian (Expandir a Pesquisa)
cent nerve » bent nerve (Expandir a Pesquisa), recent nerve (Expandir a Pesquisa), crest nerve (Expandir a Pesquisa)
nerve can » nerve canal (Expandir a Pesquisa), nerve case (Expandir a Pesquisa), nerve a (Expandir a Pesquisa)
can due » scan due (Expandir a Pesquisa), man due (Expandir a Pesquisa), can de (Expandir a Pesquisa)
i cent » i cento (Expandir a Pesquisa), ai cent (Expandir a Pesquisa), ii cent (Expandir a Pesquisa)
A mostrar 101 - 120 resultados de 161 para a pesquisa '(( i cent nerve can due ) OR ( j bennett bruce a j ))*', tempo de pesquisa: 0.75seg Refinar resultados
Retinal dystrophies, genomic applications in diagnosis and prospects for therapy
NY-ESO-1 specific TCR engineered T-cells mediate sustained antigen-specific antitumor effects in myeloma

A Genome-Wide Association Study of Aging
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

Endovascular Thrombectomy for Ischemic Stroke Increases Disability-Free Survival, Quality of Life, and Life Expectancy and Reduces Cost
Discovery of Narlaprevir (SCH 900518): A Potent, Second Generation HCV NS3 Serine Protease Inhibitor

How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
NMNAT1 variants cause cone and cone-rod dystrophy

A Genome-Wide Association Study of Depressive Symptoms
Detectable clonal mosaicism from birth to old age and its relationship to cancer

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

Genetic architecture of subcortical brain structures in 38,851 individuals
Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium

Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1
Intravenous sodium nitrite in acute ST-elevation myocardial infarction: a randomized controlled trial (NIAMI)

Novel genetic loci associated with hippocampal volume
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

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