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Results: 1-25 | 26-50 | 51-51
Results: 1-25/51
A search for parenting style: A cross-situational analysis of parental behavior
Authors: Metsapelto, RL Pulkkinen, L Poikkeus, AM
Citation: Rl. Metsapelto et al., A search for parenting style: A cross-situational analysis of parental behavior, GENET SOC G, 127(2), 2001, pp. 169-192
Molecular genetics of pseudoxanthoma elasticum: a metabolic disorder at the environment-genome interface?
Authors: Uitto, J Pulkkinen, L Ringpfeil, F
Citation: J. Uitto et al., Molecular genetics of pseudoxanthoma elasticum: a metabolic disorder at the environment-genome interface?, TRENDS MO M, 7(1), 2001, pp. 13-17
Continuity in problems of social functioning in adulthood: A cumulative perspective
Authors: Ronka, A Kinnunen, U Pulkkinen, L
Citation: A. Ronka et al., Continuity in problems of social functioning in adulthood: A cumulative perspective, J ADULT DEV, 8(3), 2001, pp. 161-171
Biology and pathology of hemidesmosomes
Authors: Pulkkinen, L Uitto, J
Citation: L. Pulkkinen et J. Uitto, Biology and pathology of hemidesmosomes, CELL ADHES, 8, 2001, pp. 107-131
Molecular genetics of pseudoxanthoma elasticum
Authors: Ringpfeil, E Pulkkinen, L Uitto, J
Citation: E. Ringpfeil et al., Molecular genetics of pseudoxanthoma elasticum, EXP DERMATO, 10(4), 2001, pp. 221-228
Examination of the paths between personality, current mood, its evaluation, and emotion regulation
Authors: Kokkonen, M Pulkkinen, L
Citation: M. Kokkonen et L. Pulkkinen, Examination of the paths between personality, current mood, its evaluation, and emotion regulation, EUR J PERS, 15(2), 2001, pp. 83-104
Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum
Authors: Pulkkinen, L Nakano, A Ringpfeil, F Uitto, J
Citation: L. Pulkkinen et al., Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum, HUM GENET, 109(3), 2001, pp. 356-365
Antenatal genetic screening for congenital nephrosis
Authors: Kallinen, J Heinonen, S Ryynanen, M Pulkkinen, L Mannermaa, A
Citation: J. Kallinen et al., Antenatal genetic screening for congenital nephrosis, PRENAT DIAG, 21(2), 2001, pp. 81-84
Drinking or abstaining at age 14? A genetic epidemiological study
Authors: Rose, RJ Dick, DM Viken, RJ Pulkkinen, L Kaprio, J
Citation: Rj. Rose et al., Drinking or abstaining at age 14? A genetic epidemiological study, ALC CLIN EX, 25(11), 2001, pp. 1594-1604
An aggression machine V. Determinants in reactive aggression revisited
Authors: Juujarvi, P Kooistra, L Kaartinen, J Pulkkinen, L
Citation: P. Juujarvi et al., An aggression machine V. Determinants in reactive aggression revisited, AGGR BEHAV, 27(6), 2001, pp. 430-445
Measuring puberty and understanding its impact: A longitudinal study of adolescent twins
Authors: Dick, DM Rose, RJ Pulkkinen, L Kaprio, J
Citation: Dm. Dick et al., Measuring puberty and understanding its impact: A longitudinal study of adolescent twins, J YOUTH ADO, 30(4), 2001, pp. 385-399
Epidermolysis bullosa with congenital pyloric atresia: Novel mutations in the beta 4 integrin gene (ITGB4) and genotype/phenotype correlations
Authors: Nakano, A Pulkkinen, L Murrell, D Rico, J Lucky, AW Garzon, M Stevens, CA Robertson, S Pfendner, E Uitto, J
Citation: A. Nakano et al., Epidermolysis bullosa with congenital pyloric atresia: Novel mutations in the beta 4 integrin gene (ITGB4) and genotype/phenotype correlations, PEDIAT RES, 49(5), 2001, pp. 618-626
Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?
Authors: Klausegger, A Pulkkinen, L Pohla-Gubo, G Dallinger, G Puttinger, R Uitto, J Hintner, H Bauer, JW
Citation: A. Klausegger et al., Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?, J INVES DER, 116(3), 2001, pp. 474-475
Papillon-Lefevre syndrome: Mutations and polymorphisms in the cathepsin C gene
Authors: Nakano, A Nomura, K Nakano, H Ono, Y LaForgia, S Pulkkinen, L Hashimoto, I Uitto, J
Citation: A. Nakano et al., Papillon-Lefevre syndrome: Mutations and polymorphisms in the cathepsin C gene, J INVES DER, 116(2), 2001, pp. 339-343
Reduced expression of the epithelial adhesion ligand laminin 5 in the skincauses intradermal tissue separation
Authors: Spirito, F Chavanas, S Prost-Squarcioni, C Pulkkinen, L Fraitag, S Bodemer, C Ortonne, JP Meneguzzi, G
Citation: F. Spirito et al., Reduced expression of the epithelial adhesion ligand laminin 5 in the skincauses intradermal tissue separation, J BIOL CHEM, 276(22), 2001, pp. 18828-18835
Widespread pain among 11-year-old Finnish twin pairs
Authors: Mikkelsson, M Kaprio, J Salminen, JJ Pulkkinen, L Rose, RJ
Citation: M. Mikkelsson et al., Widespread pain among 11-year-old Finnish twin pairs, ARTH RHEUM, 44(2), 2001, pp. 481-485
Molecular genetics of heritable blistering disorders
Authors: Uitto, J Pulkkinen, L
Citation: J. Uitto et L. Pulkkinen, Molecular genetics of heritable blistering disorders, ARCH DERMAT, 137(11), 2001, pp. 1458-1461
Compound heterozygosity for a recurrent 16.5-kb Alu-mediated deletion mutation and single-base-pair substitutions in the ABCC6 gene results in pseudoxanthoma elasticum
Authors: Ringpfeil, F Nakano, A Uitto, J Pulkkinen, L
Citation: F. Ringpfeil et al., Compound heterozygosity for a recurrent 16.5-kb Alu-mediated deletion mutation and single-base-pair substitutions in the ABCC6 gene results in pseudoxanthoma elasticum, AM J HU GEN, 68(3), 2001, pp. 642-652
The genodermatoses: Candidate diseases for gene therapy
Authors: Uitto, J Pulkkinen, L
Citation: J. Uitto et L. Pulkkinen, The genodermatoses: Candidate diseases for gene therapy, HUM GENE TH, 11(16), 2000, pp. 2267-2275
Epidermolysis bullosa, pyloric atresia, and obstructive uropathy: A reportof two case reports with molecular correlation and clinical management
Authors: Wallerstein, R Klein, ML Genieser, N Pulkkinen, L Uitto, J
Citation: R. Wallerstein et al., Epidermolysis bullosa, pyloric atresia, and obstructive uropathy: A reportof two case reports with molecular correlation and clinical management, PEDIAT DERM, 17(4), 2000, pp. 286-289
Cutaneous gene therapy - Principles and prospects
Authors: Lin, MTS Pulkkinen, L Uitto, J
Citation: Mts. Lin et al., Cutaneous gene therapy - Principles and prospects, DERM CLIN, 18(1), 2000, pp. 177
A de novo glycine substitution mutation in the collagenous domain of COL7A1 in dominant dystrophic epidermolysis bullosa
Authors: Lee, JYY Li, C Chao, SC Pulkkinen, L Uitto, J
Citation: Jyy. Lee et al., A de novo glycine substitution mutation in the collagenous domain of COL7A1 in dominant dystrophic epidermolysis bullosa, ARCH DERM R, 292(4), 2000, pp. 159-163
Congenital focal segmental glomerulosclerosis associated with beta 4 integrin mutation and epidermolysis bullosa
Authors: Kambham, N Tanji, N Seigle, RL Markowitz, GS Pulkkinen, L Uitto, J D'Agati, VD
Citation: N. Kambham et al., Congenital focal segmental glomerulosclerosis associated with beta 4 integrin mutation and epidermolysis bullosa, AM J KIDNEY, 36(1), 2000, pp. 190-196
The accumulation of problems of social functioning as a long-term process:Women and men compared
Authors: Ronka, A Kinnunen, U Pulkkinen, L
Citation: A. Ronka et al., The accumulation of problems of social functioning as a long-term process:Women and men compared, INT J BEHAV, 24(4), 2000, pp. 442-450
Selection into long-term unemployment and its psychological consequences
Authors: Kokko, K Pulkkinen, L Puustinen, M
Citation: K. Kokko et al., Selection into long-term unemployment and its psychological consequences, INT J BEHAV, 24(3), 2000, pp. 310-320
Risultati: 1-25 | 26-50 | 51-51