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Results: 51-75/95
Authors:
Aho, S
Buisson, M
Pajunen, T
Ryoo, YW
Giot, JF
Gruffat, H
Sergeant, A
Uitto, J
Citation: S. Aho et al., Ubinuclein, a novel nuclear protein interacting with cellular and viral transcription factors, J CELL BIOL, 148(6), 2000, pp. 1165-1176
Authors:
Ghohestani, RF
Hudson, BG
Claudy, A
Uitto, J
Citation: Rf. Ghohestani et al., The alpha 5 chain of type IV collagen is the target of IgG autoantibodies in a novel autoimmune disease with subepidermal blisters and renal insufficiency, J BIOL CHEM, 275(21), 2000, pp. 16002-16006
Authors:
Mongiat, M
Taylor, K
Otto, J
Aho, S
Uitto, J
Whitelock, JM
Iozzo, RV
Citation: M. Mongiat et al., The protein core of the proteoglycan perlecan binds specifically to fibroblast growth factor-7, J BIOL CHEM, 275(10), 2000, pp. 7095-7100
Authors:
Corden, LD
Swensson, O
Swensson, B
Smith, FJD
Rochels, R
Uitto, J
McLean, WHI
Citation: Ld. Corden et al., Molecular genetics of Meesmann's corneal dystrophy: Ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene, EXP EYE RES, 70(1), 2000, pp. 41-49
Authors:
Uitto, J
Pulkkinen, L
Citation: J. Uitto et L. Pulkkinen, Epidermolysis bullosa in Mexico, INT J DERM, 39(6), 2000, pp. 433-435
Authors:
Lin, MTS
Pulkkinen, L
Uitto, J
Yoon, K
Citation: Mts. Lin et al., The gene gun: current applications in cutaneous gene therapy, INT J DERM, 39(3), 2000, pp. 161-170
Authors:
Morrell, DS
Rubenstein, DS
Briggaman, RA
Fine, JD
Pulkkinen, L
Uitto, J
Citation: Ds. Morrell et al., Congenital pyloric atresia in a newborn with extensive aplasia cutis congenita and epidermolysis bullosa simplex, BR J DERM, 143(6), 2000, pp. 1342-1343
Authors:
Chavanas, S
Gache, Y
Vailly, J
Kanitakis, J
Pulkkinen, L
Uitto, J
Ortonne, JP
Meneguzzi, G
Citation: S. Chavanas et al., Splicing modulation of integrin beta 4 pre-mRNA carrying a branch point mutation underlies epidermolysis bullosa with pyloric atresia undergoing spontaneous amelioration with ageing, HUM MOL GEN, 8(11), 1999, pp. 2097-2105
Cooperation between SMAD and NF-kappa B in growth factor regulated type VII collagen gene expression
Authors:
Kon, A
Vindevoghel, L
Kouba, DJ
Fujimura, Y
Uitto, J
Mauviel, A
Citation: A. Kon et al., Cooperation between SMAD and NF-kappa B in growth factor regulated type VII collagen gene expression, ONCOGENE, 18(10), 1999, pp. 1837-1844
Authors:
Pulkkinen, L
Uitto, J
Citation: L. Pulkkinen et J. Uitto, Mutation analysis and molecular genetics of epidermolysis bullosa, MATRIX BIOL, 18(1), 1999, pp. 29-42
Authors:
Kivirikko, S
Mauviel, A
Pihlajaniemi, T
Uitto, J
Citation: S. Kivirikko et al., Cytokine modulation of type XV collagen gene expression in human dermal fibroblast cultures, EXP DERMATO, 8(5), 1999, pp. 407-412
Authors:
Uitto, J
Citation: J. Uitto, Molecular diagnostics of epidermolysis bullosa: novel pathomechanisms and surprising genetics, EXP DERMATO, 8(2), 1999, pp. 92-95
Authors:
Smith, FJD
McKenna, KE
Irvine, AD
Bingham, EA
Coleman, CM
Uitto, J
McLean, WHI
Citation: Fjd. Smith et al., A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1, EXP DERMATO, 8(2), 1999, pp. 109-114
Authors:
Hashimoto, I
Kon, A
Tamai, K
Uitto, J
Citation: I. Hashimoto et al., Diagnostic dilemma of "sporadic" cases of dystrophic epidermolysis bullosa: a new dominant or mitis recessive mutation?, EXP DERMATO, 8(2), 1999, pp. 140-142
Authors:
Christiano, AM
Crollick, J
Pincus, S
Uitto, J
Citation: Am. Christiano et al., Squamous cell carcinoma in a family with dominant dystrophic epidermolysisbullosa: a molecular genetic study, EXP DERMATO, 8(2), 1999, pp. 146-152
Authors:
Aho, S
Rothenberger, K
Tan, EML
Ryoo, YW
Cho, BH
McLean, WHI
Uitto, J
Citation: S. Aho et al., Human periplakin: Genomic organization in a clonally unstable region of chromosome 16p with an abundance of repetitive sequence elements, GENOMICS, 56(2), 1999, pp. 160-168
Authors:
Aho, S
Rothenberger, K
Uitto, J
Citation: S. Aho et al., Human p120(ctn) catenin: Tissue-specific expression of isoforms and molecular interactions with BP180 type XVII collagen, J CELL BIOC, 73(3), 1999, pp. 390-399
Authors:
Aho, S
Uitto, J
Citation: S. Aho et J. Uitto, 180-kD bullous pemphigoid antigen type XVII collagen: Tissue-specific expression and molecular interactions with keratin 18, J CELL BIOC, 72(3), 1999, pp. 356-367
Authors:
Uitto, J
Citation: J. Uitto, Molecular genetics of the cutaneous basement membrane zone: clinical implications of basic research on epidermolysis bullosa, INT CONGR S, 1172, 1999, pp. 3-20
Authors:
Tamai, K
Murai, T
Mayama, M
Kon, A
Sawamura, D
Nomura, K
Hanada, K
Hashimoto, I
Uitto, J
Citation: K. Tamai et al., Recent studies on DNA-based diagnosis for Japanese cases of dystrophic epidermolysis bullosa, INT CONGR S, 1172, 1999, pp. 53-61
Authors:
Atsushi, K
Vindevoghel, L
Hashimoto, I
Uitto, J
Mauviel, A
Citation: K. Atsushi et al., TGF-beta/Smad and TNF-alpha/NF-kappa B upregulate type VII collagen gene expression additively at the transcriptional level, INT CONGR S, 1172, 1999, pp. 175-183
Authors:
Shimizu, H
Masunaga, T
Kurihara, Y
Owaribe, K
Wiche, G
Pulkkinen, L
Uitto, J
Nishikawa, T
Citation: H. Shimizu et al., Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy, ARCH DERM R, 291(10), 1999, pp. 531-537
Authors:
Lakkakorpi, J
Li, KH
Decker, S
Korkeela, E
Piddington, R
Abrams, W
Bashir, M
Uitto, J
Rosenbloom, J
Citation: J. Lakkakorpi et al., Expression of the elastin promoter in novel tissue sites in transgenic mouse embryos, CONNECT TIS, 40(2), 1999, pp. 155
Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1
Authors:
Smith, FJD
McKusick, VA
Nielsen, K
Pfendner, E
Uitto, J
McLean, WHI
Citation: Fjd. Smith et al., Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1, PRENAT DIAG, 19(10), 1999, pp. 941-946
Authors:
Shimizu, H
Takizawa, Y
Pulkkinen, L
Murata, S
Kawai, M
Hachisuka, H
Udono, M
Uitto, J
Nishikawa, T
Citation: H. Shimizu et al., Epidermolysis bullosa simplex associated with muscular dystrophy: Phenotype-genotype correlations and review of the literature, J AM ACAD D, 41(6), 1999, pp. 950-956