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Research 211–240 of 446
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- FOXN1 deficient nude severe combined immunodeficiency
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Genetic Disorders and Defects in Vitamin D Action
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Myotonic Dystrophy—A Progeroid Disease?
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Molecular pathways involved in hair follicle tumor formation: all about mammalian target of rapamycin?
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Atrichia with papular lesions
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
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- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Congenital Adrenal Hyperplasia
- Decision letter: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- Generalized atrophic benign epidermolysis bullosa.
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Identification and characterization of genes for skin and hair disorders
- Drug Repurposing Patent Applications April–June 2021
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- WNT Signaling in Disease
- Regulatory T Cells: the Many Faces of Foxp3