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Research 91–120 of 1000+
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Madarosis: A marker of many Maladies
- Tissue engineering of skin and regenerative medicine for wound care
- The Roles of Non-coding RNA in the Development and Regeneration of Hair Follicles: Current Status and Further Perspectives
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- The Role of Vitamin D and Testosterone Levels with Hair Loss among Females with Coronavirus Disease
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- X linked mental retardation.
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Male-Pattern Baldness in Men with X-Linked Recessive Ichthyosis
- Absence of Male-Pattern Baldness in Men with X-Linked Recessive Ichthyosis?
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Male-Pattern Baldness Is Common in Men with X-Linked Recessive Ichthyosis
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- An unusual presentation of X-linked adrenoleukodystrophy
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Infantile vitiligo and alopecia in immunodysregulation polyendocrinopathy enteropathy X‐linked syndrome
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- More about X‐linked testicular feminization of the mouse as a noninducible (i<sup>s</sup>) mutation of a regulatory locus: 5α‐androstan‐3α‐17ß‐diol as the true inducer of kidney alcohol dehydrogenase and ß‐glucuronidase
- Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy
- Lupus erythematosus-like lesions in a carrier of X-linked chronic granulomatous disease: A case report and personal considerations
- INVESTIGATIONS INTO THE ROLE OF THE X-LINKED EPIGENETIC REGULATOR UTX (KDM6A) IN SELF-RENEWING STRATIFYING EPITHELIA
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition