about
rs929387 of GLI3 is involved in tooth agenesis in Chinese Han population.Association between rs11001553 of DKK1 and non-syndromic tooth agenesis in the Chinese Han population.Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.Dopaminergic effects on in vitro osteogenesis.Mutations in WNT10B Are Identified in Individuals with OligodontiaSenescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia.Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis.Rubicon: LC3-associated phagocytosis and beyond.Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.Dopaminergic enhancement of cellular adhesion in bone marrow derived mesenchymal stem cells (MSCs).Dramatic Improvement of the Mechanical Strength of Silane-Modified Hydroxyapatite-Gelatin Composites via Processing with Cosolvent.More Than Skin Deep: Autophagy Is Vital for Skin Barrier Function.Programmed Necrosis and Disease:We interrupt your regular programming to bring you necroinflammationNovel missense mutations in the AXIN2 gene associated with non-syndromic oligodontiaA novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontiaGenetic analysis: Wnt and other pathways in nonsyndromic tooth agenesisNovel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesisDistinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasiaTooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disordersGlobal deletion of Optineurin results in altered type I IFN signaling and abnormal bone remodeling in a model of Paget's diseaseCDDO-Me, Sulforaphane and tBHQ attenuate the RANKL-induced osteoclast differentiation via activating the NRF2-mediated antioxidant responseBMP4 mutations in tooth agenesis and low bone massA novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis
P50
Q35053744-3923768E-AB97-46AD-9C58-3CF37C35D9ADQ35149768-869316C0-5A53-4FB1-811D-BC561D9E15B3Q35672195-160735A4-2E71-4EF6-AF88-E25A942EDF1FQ36266555-61473A9B-57CA-41FE-9F53-775A61B12C1EQ37218485-34169662-438E-432D-BC98-FFF8A5F9ED53Q37479739-035EEACF-1121-4F70-8A72-0E116E09EE1FQ40250208-BCB31D21-927D-469D-8769-FC8E62A4A2A4Q47248157-0ECEAF5D-FDAB-45E6-B1A9-589143C231E7Q47568393-8147159C-5751-4E01-8CF9-E44A3A31BA28Q47675814-792BF328-18C6-42FB-A5AB-8E78C971D26CQ49315962-EB997359-2E1B-4179-A742-4C37E95197D5Q52603484-C559A38A-0EE8-4FD6-AEB9-0011D697A759Q55455268-9597A259-3561-4301-9497-98E9CFBC8963Q57801723-38A2E8A0-AF09-4082-98AE-5F77FB39271CQ87383208-6F879036-8EBE-4050-9F9A-2FB432D83B99Q88048453-A5AC5B40-AF1B-42D7-B5BF-E3A55CB95F13Q89406490-6E784C7D-646F-4DB7-B58D-2A5F285EBD78Q90142009-DC7197C9-CB1B-4C26-8D0F-6F1B975C7A48Q90656930-771077AB-3FA9-4B97-BDF3-124A2F09C6C1Q91724667-6F742F32-A914-4AD8-83F8-E64139A68A9FQ91931290-7F195FC3-B33B-405C-960D-56B099F2EBE9Q92072047-9AEFF9D3-01E6-431A-92FE-DBF1EDDF9434Q92290039-14E447EA-C358-497C-B728-60A1BB895C58Q92629260-CC480DDA-F273-4A94-9293-57FB0A750B3B
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sing-Wai Wong
@ast
Sing-Wai Wong
@en
Sing-Wai Wong
@es
Sing-Wai Wong
@nl
Sing-Wai Wong
@sl
type
label
Sing-Wai Wong
@ast
Sing-Wai Wong
@en
Sing-Wai Wong
@es
Sing-Wai Wong
@nl
Sing-Wai Wong
@sl
prefLabel
Sing-Wai Wong
@ast
Sing-Wai Wong
@en
Sing-Wai Wong
@es
Sing-Wai Wong
@nl
Sing-Wai Wong
@sl
P106
P1153
56009778900
P21
P31
P496
0000-0002-6905-3050