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Research 61–90 of 85
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin
- Biliary fibrosis is an important but neglected pathological feature in hepatobiliary disorders: from molecular mechanisms to clinical implications
- Stimuli-responsive Hydrogels: An Intelligent Tool for Wound Management
- Signal detection between 5-alpha reductase inhibitors and the risk of suicidality and depression: an international pharmacovigilance analysis
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Lean Women with Polycystic Ovary Syndrome
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Modulating the Gut–Skin Axis in Dermatological Diseases: Mechanisms and Clinical Applications of Probiotics, Prebiotics, Synbiotics, and Postbiotics
- New insights into the phenomenon of remissions and relapses in autoimmune diseases and the puzzle of benign autoantibodies in healthy individuals
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Commonly encountered symptoms and their management in patients with cirrhosis
- From bench to babies – drug development for male subfertility
- Comparative efficacy and safety of JAK inhibitors in the treatment of moderate-to-severe alopecia areata: a systematic review and network meta-analysis
- Spontaneous Lesions of Endangered Geriatric Julia Creek Dunnarts (Sminthopsis douglasi, Archer 1979) with Emphasis in Reproductive Pathology
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Multiple Autoimmune Syndrome With Alopecia Universalis and Immune Thrombocytopenic Purpura
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Hair & Cutaneous Development
- This Month in the Journal
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Chronic Pancreatitis and Persistent Steatorrhea: What Is the Correct Dose of Enzymes?
- Managing polycystic ovary syndrome in primary care