Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin–Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome

Dawn H. Siegel, G H S Ashton, Homero Penagos, +39

The American Journal of Human Genetics

Causes Kindler SyndromeGenetic DisorderGeneticsProtein GeneticsMolecular Genetics +6

Autoantibodies to extracellular matrix protein 1 in lichen sclerosus

Noritaka Oyama, Ien Chan, S. M. Neill, +8

The Lancet

Autoimmune DiseaseAutoantibody ProductionSystemic SclerodermaImmunologyHistopathology +7

Extracellular Matrix Protein 1 Gene (ECM1) Mutations in Lipoid Proteinosis and Genotype-Phenotype Correlation

Takahiro Hamada, Vesarat Wessagowit, Andrew P. South, +18

Journal of Investigative Dermatology

GeneticsExtracellular MatrixLipoid ProteinosisMedicineCell Biology +1

Complete Maternal Isodisomy of Chromosome 3 in a Child with Recessive Dystrophic Epidermolysis Bullosa but No Other Phenotypic Abnormalities

Hiva Fassihi, Lu Liu, Vesarat Wessagowit, +7

Journal of Investigative Dermatology

Complete Maternal IsodisomyGynecologyChromosome 3DermatologyMedicine +1

Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene

Cristina Has, Vesarat Wessagowit, Monica Pascucci, +12

Journal of Investigative Dermatology

Mendelian DisorderGenetic DisorderGeneticsKind1 GeneMolecular Biology +8

Heterozygous germline missense mutation in the <i>p63</i> gene underlying EEC syndrome

Vesarat Wessagowit, Jemima E. Mellerio, A.C. Pembroke, +1

Clinical and Experimental Dermatology

Cleft LipEec SyndromeDevelopmental BiologyMendelian DisorderGenetic Disorder +10

Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa

Hiva Fassihi, Vesarat Wessagowit, G H S Ashton, +5

Clinical and Experimental Dermatology

Mendelian DisorderCell DivisionCytogeneticsMedicineGenetics +13

Transient bullous dermolysis of the newborn in three generations

Hiva Fassihi, V. C. Diba, Vesarat Wessagowit, +4

British Journal of Dermatology

Animal PhysiologyType Vii CollagenAnimal ScienceTransient Bullous DermolysisHistopathology +13

A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets

Ken Arita, Arti Nanda, Vesarat Wessagowit, +3

British Journal of Dermatology

Novel MutationGenetic DisorderGeneticsPathogenesisMolecular Biology +3

Treatment of male androgenetic alopecia with topical products containing <scp><i>S</i></scp><i>erenoa repens</i> extract

Vesarat Wessagowit, Chinmanat Tangjaturonrusamee, Tanawatt Kootiratrakarn, +4

Australasian Journal of Dermatology