Found: 16
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Oestriol and oestradiol increase cell to cell communication and connexin43 protein expression in human myometrium.
- Published in:
- Molecular Human Reproduction, 2001, v. 7, n. 7, doi. 10.1093/molehr/7.7.671
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- Article
The pineal and extra-pineal origins of 5-sulphatoxy N-acetyl-serotonin in humans.
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- Journal of Pineal Research, 1999, v. 26, n. 4, p. 221, doi. 10.1111/j.1600-079X.1999.tb00587.x
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- Article
An enzyme immunoassay for 6-sulphatoxy-melatonin in human urine.
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- Journal of Pineal Research, 1996, v. 20, n. 2, p. 51, doi. 10.1111/j.1600-079X.1996.tb00239.x
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- Article
Elevated Nocturnal Melatonin Is a Consequence of Gonadotropin-Releasing Hormone Deficiency in Women with Hypothalamic Amenorrhea.
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- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 10, p. 3653, doi. 10.1210/jcem.83.10.5155
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- Article
O18 Precision genome editing for targeted correction of pathogenic D50N mutation in keratitis–ichthyosis–deafness syndrome using CRISPR/Cas9 and homology-directed repair.
- Published in:
- British Journal of Dermatology, 2024, v. 190, n. 6, p. e76, doi. 10.1093/bjd/ljae105.018
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- Article
P20 Engineered peptide for KLK5 inhibition – therapeutic intervention for atopic dermatitis.
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- British Journal of Dermatology, 2023, v. 189, n. 1, p. e22, doi. 10.1093/bjd/ljad174.041
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- Article
P09 Short-term rho-associated kinase inhibitor treatment promotes primary keratinocyte growth without affecting keratinocyte stem cell properties.
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- British Journal of Dermatology, 2023, v. 189, n. 1, p. e17, doi. 10.1093/bjd/ljad174.031
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- Article
Ex vivo gene modification therapy for genetic skin diseases—recent advances in gene modification technologies and delivery.
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- Experimental Dermatology, 2021, v. 30, n. 7, p. 887, doi. 10.1111/exd.14314
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- Article
Case Report: ISG15 deficiency caused by novel variants in two families and effective treatment with Janus kinase inhibition.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1287258
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- Article
Multiple Epidermal Connexins are Expressed in Different Keratinocyte Subpopulations Including Connexin 31.
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- Journal of Investigative Dermatology, 2001, v. 117, n. 4, p. 958, doi. 10.1046/j.0022-202X.2001.01468.x
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- Article
Tissue Kallikrein Inhibitors Based on the Sunflower Trypsin Inhibitor Scaffold – A Potential Therapeutic Intervention for Skin Diseases.
- Published in:
- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0166268
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- Article
Harlequin ichthyosis: ABCA12 mutations underlie defective lipid transport, reduced protease regulation and skin-barrier dysfunction.
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- Cell & Tissue Research, 2013, v. 351, n. 2, p. 281, doi. 10.1007/s00441-012-1474-9
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- Article
Ex-vivo Gene Therapy Restores LEKTI Activity and Corrects the Architecture of Netherton Syndrome-derived Skin Grafts.
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- Molecular Therapy, 2011, v. 19, n. 2, p. 408, doi. 10.1038/mt.2010.201
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- Article
Short-Term Treatment with Rho-Associated Kinase Inhibitor Preserves Keratinocyte Stem Cell Characteristics In Vitro.
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- Cells (2073-4409), 2023, v. 12, n. 3, p. 346, doi. 10.3390/cells12030346
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- Article
Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations.
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- Human Molecular Genetics, 2002, v. 11, n. 17, p. 2005
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- Article
A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 11, p. 1311, doi. 10.1093/hmg/11.11.1311
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- Article