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Research 211–240 of 1000+
- 0748 Synergy of TP53 and non-canonical sonic hedgehog pathway in the development of complex basal cell carcinoma
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- A BIOCHEMICAL MARKER IN A DOMINANT MOUSE TRAIT
- Epidermolysis Bullosa in Calves in the United Kingdom
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- 545 Skin Organoids derived from NCSTN mutated patient-induced pluripotent stem cells recapitulate Hidradenitis Suppurativa pathogenic hallmarks
- Salt-losing tubulopathy and chronic dermatitis
- Berardinelli–Seip syndrome
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- The color of human hair
- Clinical and molecular genetic studies in hereditary hair loss
- A newborn presenting with congenital blistering
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- A new type of pachyonychia congenita.
- Observational Study of Paclitaxel-Carboplatin versus Pemetrexed-Carboplatin for Advanced Pulmonary Adenocarcinoma at Single-Centre in Indonesia
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- <i>CCDC47</i> gene and trichohepatoneurodevelopmental syndrome: Report of the fifth and sixth cases from Saudi Arabia
- Attention to Innate Circadian Rhythm and the Impact of Its Disruption on Diabetes
- Epidermolysis bullosa in calves in the United Kingdom
- Caractérisation d’une modification «bigarré» de la couleur du pelage chez le chat domestique
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Molecular landscape of lung cancer: insights into therapeutic targets and clinical outcomes
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- 14-3-3σ Is Required for Club Hair Retention
- Nonclassic adrenal hyperplasia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype