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Investigation of the Possible Role of WNT Genes in Human Breast Cancer.
- Published in:
- Annals of the New York Academy of Sciences, 1995, v. 768, n. 1, p. 257, doi. 10.1111/j.1749-6632.1995.tb12134.x
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- Publication type:
- Article
Human Population Expansion and Microsatellite Variation.
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- Molecular Biology & Evolution, 2000, v. 17, n. 5, p. 757, doi. 10.1093/oxfordjournals.molbev.a026354
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- Publication type:
- Article
CORRIGENDUM: Getting under the skin: the immunogenetics of psoriasis.
- Published in:
- 2005
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- Publication type:
- Correction notice
Getting under the skin: the immunogenetics of psoriasis.
- Published in:
- Nature Reviews Immunology, 2005, v. 5, n. 9, p. 699, doi. 10.1038/nri1689
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- Publication type:
- Article
Peptidoglycan recognition proteins Pglyrp3 and Pglyrp4 are encoded from the epidermal differentiation complex and are candidate genes for the Psors4 locus on chromosome 1q21.
- Published in:
- Human Genetics, 2006, v. 119, n. 1/2, p. 113, doi. 10.1007/s00439-005-0115-8
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- Publication type:
- Article
Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR.
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- Human Genetics, 2005, v. 118, n. 3/4, p. 466, doi. 10.1007/s00439-005-0048-2
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- Publication type:
- Article
SNTG1, the gene encoding γ1-syntrophin: a candidate gene for idiopathic scoliosis.
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- Human Genetics, 2004, v. 115, n. 1, p. 81, doi. 10.1007/s00439-004-1121-y
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- Publication type:
- Article
Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility.
- Published in:
- Human Genetics, 2003, v. 112, n. 1, p. 34, doi. 10.1007/s00439-002-0851-y
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- Publication type:
- Article
Breast Cancer Genes.
- Published in:
- Breast Journal, 1997, v. 3, n. S1, p. 1, doi. 10.1111/j.1524-4741.1997.tb00200.x
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- Publication type:
- Article
Conservation of function and primary structure in the BRCA1-associated RING domain (BARD1) protein.
- Published in:
- Oncogene, 1998, v. 17, n. 16, p. 2143, doi. 10.1038/sj.onc.1202123
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- Publication type:
- Article
In vitro transformation of cell lines from human salivary gland tumors.
- Published in:
- International Journal of Cancer, 1999, v. 81, n. 5, p. 793, doi. 10.1002/(SICI)1097-0215(19990531)81:5<793::AID-IJC21>3.0.CO;2-4
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- Publication type:
- Article
The Tetratricopeptide Repeat Domain 7 Gene is Mutated in Flaky Skin Mice: A Model for Psoriasis, Autoimmunity, and Anemia.
- Published in:
- Experimental Biology & Medicine, 2005, v. 230, n. 9, p. 659, doi. 10.1177/153537020523000908
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- Publication type:
- Article
Genomics: Guilt by association.
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- Nature, 2007, v. 447, n. 7145, p. 645, doi. 10.1038/447645a
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- Publication type:
- Article
Completing the map of human genetic variation.
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- Nature, 2007, v. 447, n. 7141, p. 161, doi. 10.1038/447161a
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- Publication type:
- Article
Pathogenesis and therapy of psoriasis.
- Published in:
- Nature, 2007, v. 445, n. 7130, p. 866, doi. 10.1038/nature05663
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- Publication type:
- Article
Psoriasis: genetic associations and immune system changes.
- Published in:
- Genes & Immunity, 2007, v. 8, n. 1, p. 1, doi. 10.1038/sj.gene.6364351
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- Publication type:
- Article
Deletion of the activating NKG2C receptor and a functional polymorphism in its ligand HLA-E in psoriasis susceptibility.
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- Experimental Dermatology, 2013, v. 22, n. 10, p. 679, doi. 10.1111/exd.12233
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- Publication type:
- Article
Contribution of genetic factors for melanoma susceptibility in sporadic US melanoma patients.
- Published in:
- 2009
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- Publication type:
- Letter
Nifedipine in the treatment of Raynaud's phenomenon in patients with systemic sclerosis.
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- British Journal of Dermatology, 1987, v. 117, n. 2, p. 237, doi. 10.1111/j.1365-2133.1987.tb04122.x
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- Publication type:
- Article
Noncanonical microRNAs and endogenous siRNAs in normal and psoriatic human skin.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 4, p. 737, doi. 10.1093/hmg/dds481
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- Publication type:
- Article
Deep sequencing of small RNAs from human skin reveals major alterations in the psoriasis miRNAome.
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- Human Molecular Genetics, 2011, v. 20, n. 20, p. 4025, doi. 10.1093/hmg/ddr331
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- Publication type:
- Article
The genetics of psoriasis, psoriatic arthritis and atopic dermatitis.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R43
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- Publication type:
- Article
Punctuated evolution of canonical genomic aberrations in uveal melanoma.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02428-w
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- Publication type:
- Article
Fine mapping of eight psoriasis susceptibility loci.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 844, doi. 10.1038/ejhg.2014.172
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- Publication type:
- Article
A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.
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- European Journal of Human Genetics, 2004, v. 12, n. 9, p. 752, doi. 10.1038/sj.ejhg.5201219
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- Publication type:
- Article
Genomic Analysis Defines a Cancer-Specific Gene Expression Signature for Human Squamous Cell Carcinoma and Distinguishes Malignant Hyperproliferation from Benign Hyperplasia.
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- Journal of Investigative Dermatology, 2006, v. 126, n. 4, p. 869, doi. 10.1038/sj.jid.5700157
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- Publication type:
- Article
Investigation of the Chromosome 17q25 PSORS2 Locus in Atopic Dermatitis.
- Published in:
- Journal of Investigative Dermatology, 2006, v. 126, n. 3, p. 603, doi. 10.1038/sj.jid.5700108
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- Publication type:
- Article
Psoriasis Genetics: The Way Forward.
- Published in:
- 2004
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- Publication type:
- Editorial
Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma.
- Published in:
- Nature Genetics, 2013, v. 45, n. 2, p. 133, doi. 10.1038/ng.2523
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- Publication type:
- Article
Genome-wide association analysis identifies three psoriasis susceptibility loci.
- Published in:
- Nature Genetics, 2010, v. 42, n. 11, p. 1000, doi. 10.1038/ng.693
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- Publication type:
- Article
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis.
- Published in:
- Nature Genetics, 2003, v. 35, n. 4, p. 349, doi. 10.1038/ng1268
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- Publication type:
- Article
Psoriasis Patients Are Enriched for Genetic Variants That Protect against HIV-1 Disease.
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- PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002514
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- Publication type:
- Article
Multiple Loci within the Major Histocompatibility Complex Confer Risk of Psoriasis.
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- PLoS Genetics, 2009, v. 5, n. 8, p. 1, doi. 10.1371/journal.pgen.1000606
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- Publication type:
- Article
A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci.
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- PLoS Genetics, 2008, v. 4, n. 4, p. 1, doi. 10.1371/journal.pgen.1000041
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- Publication type:
- Article
Psoriasis mutations disrupt CARD14 autoinhibition promoting BCL10-MALT1-dependent NF-κB activation.
- Published in:
- Biochemical Journal, 2016, v. 473, n. 12, p. 1759, doi. 10.1042/BCJ20160270
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- Publication type:
- Article
CARD14‐associated papulosquamous eruption (CAPE) in pediatric patients: Three additional cases and review of the literature.
- Published in:
- Pediatric Dermatology, 2021, v. 38, n. 5, p. 1237, doi. 10.1111/pde.14779
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- Publication type:
- Article
Combined PKC and MEK inhibition for treating metastatic uveal melanoma.
- Published in:
- Oncogene, 2014, v. 33, n. 39, p. 4722, doi. 10.1038/onc.2013.555
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- Publication type:
- Article
Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases.
- Published in:
- Genes & Immunity, 2015, v. 16, n. 2, p. 120, doi. 10.1038/gene.2014.75
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- Publication type:
- Article
CARD14 Expression in Dermal Endothelial Cells in Psoriasis.
- Published in:
- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111255
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- Publication type:
- Article
A Genetic Risk Score Combining Ten Psoriasis Risk Loci Improves Disease Prediction.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019454
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- Publication type:
- Article
AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.
- Published in:
- Nature Genetics, 2002, v. 31, n. 1, p. 21, doi. 10.1038/ng880
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- Publication type:
- Article
Phenotypic Heterogeneity in Patients with Familial Partial Lipodystrophy (Dunnigan Variety) Related to the Site of Missense Mutations in Lamin A/C Gene.
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- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 1, p. 59, doi. 10.1210/jcem.86.1.7121
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- Publication type:
- Article
A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 9, p. 3390, doi. 10.1210/jcem.84.9.6103
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- Publication type:
- Article
Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety.
- Published in:
- 2003
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- Publication type:
- journal article
Biology of advanced uveal melanoma and next steps for clinical therapeutics.
- Published in:
- Pigment Cell & Melanoma Research, 2015, v. 28, n. 2, p. 135, doi. 10.1111/pcmr.12304
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- Publication type:
- Article
HOXD10 M319K mutation in a family with isolated congenital vertical talus.
- Published in:
- Journal of Orthopaedic Research, 2006, v. 24, n. 3, p. 448, doi. 10.1002/jor.20052
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- Publication type:
- Article
Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation
- Published in:
- Journal of Orthopaedic Research, 2005, v. 23, n. 6, p. 1490, doi. 10.1016/j.orthres.2005.04.011.1100230636
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- Publication type:
- Article
Driver Mutations in Uveal Melanoma: Associations With Gene Expression Profile and Patient Outcomes.
- Published in:
- 2016
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- Publication type:
- journal article
BAP1 deficiency causes loss of melanocytic cell identity in uveal melanoma.
- Published in:
- 2013
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- Publication type:
- journal article
Nonrandom Distribution of N-myc Oncogene Genotypes in Neuroblastoma.
- Published in:
- JNCI: Journal of the National Cancer Institute, 1991, v. 83, n. 15, p. 1085
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- Publication type:
- Article