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company causes » company case (Expandir a Pesquisa), company raises (Expandir a Pesquisa), company uses (Expandir a Pesquisa)
complex vague » complex value (Expandir a Pesquisa), complex vagus (Expandir a Pesquisa), complex valued (Expandir a Pesquisa)
null company » coll company (Expandir a Pesquisa), ill company (Expandir a Pesquisa), mill company (Expandir a Pesquisa)
msc complex » bmsc complex (Expandir a Pesquisa), rsc complex (Expandir a Pesquisa), tsc complex (Expandir a Pesquisa)
campo con » campo como (Expandir a Pesquisa), campo c (Expandir a Pesquisa)
al campo » el campo (Expandir a Pesquisa), del campo (Expandir a Pesquisa), al cambio (Expandir a Pesquisa)
con net » con nee (Expandir a Pesquisa), non net (Expandir a Pesquisa), upon net (Expandir a Pesquisa)
n msc » rn msc (Expandir a Pesquisa), n myc (Expandir a Pesquisa), _ msc (Expandir a Pesquisa)
j al » j a (Expandir a Pesquisa), j l (Expandir a Pesquisa)
ngoc » ngo (Expandir a Pesquisa)
A mostrar 1 - 20 resultados de 44 para a pesquisa '(( j al campo con net ) OR ((( n msc complex vague ngoc ) OR ( a null company causes non ))))', tempo de pesquisa: 1.12seg Refinar resultados
Scaffold attachment factor B2 (SAFB2)-null mice reveal non-redundant functions of SAFB2 compared with its paralog, SAFB1
Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation

PKCδ null mutations in a mouse model of osteoarthritis alter osteoarthritic pain independently of joint pathology by augmenting NGF/TrkA-induced axonal outgrowth
Neuralgia del trigémino: estudio funcional mediante tensor de difusión de alta densidad como herramienta diagnóstica

Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P
Fascin 1 is transiently expressed in mouse melanoblasts during development and promotes migration and proliferation

β-catenin regulates Pax3 and Cdx2 for caudal neural tube closure and elongation
Deletion of a single allele of the Pex11β gene is sufficient to cause oxidative stress, delayed differentiation and neuronal death in mouse brain

A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3
Delineation of proteolytic and non-proteolytic functions of the membrane-anchored serine protease prostasin

Developmental and Degenerative Features in a Complicated Spastic Paraplegia
Non-muscle Mlck is required for β-catenin- and FoxO1-dependent downregulation of Cldn5 in IL-1β-mediated barrier dysfunction in brain endothelial cells

Phenotypic spectrum of typical CHARGE syndrome in a Chinese male neonate: a case report
1-Aminocyclopropane-1-carboxylic acid as a signalling molecule in plants

A small heat shock protein is essential for thermotolerance and intracellular survival of Leishmania donovani
Examining the relationship between household air pollution and infant microbial nasal carriage in a Ghanaian cohort

Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase
PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress

Impaired remodeling phase of fracture repair in the absence of matrix metalloproteinase-2
Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development

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