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Research 631–660 of 1000+
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- The molecular basis of human keratin disorders
- Preclinical Pharmacology, Antitumor Activity, and Development of Pharmacodynamic Markers for the Novel, Potent AKT Inhibitor CCT128930
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- Pili Annulati
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- A different approach to PCOS: evaluation of spermiogram results in male patients with a family history of PCOS
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Testosterone: The Male Sex Hormone
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Cutaneous and Oral Mucosal Lesions in Cri-du-chat Syndrome
- The Case | Bilateral kidney tumors and lung cysts
- Generalised Glucocorticoid Resistance
- Toxic and Metabolic Disorders of the Nervous System
- Female Androgenetic (?) Alopecia
- The chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Laminin-511, inducer of hair growth, is down-regulated and its suppressor in hair growth, laminin-332 up-regulated in chemotherapy-induced alopecia
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant