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Research 91–120 of 1000+
- X linked mental retardation.
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- 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
- Linking allergy to mercury to HLA and burning mouth syndrome
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- I‐Ascorbic acid 2‐phosphate represses the dihydrotestosterone‐induced dickkopf‐1 expression in human balding dermal papilla cells
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Commentary 2
- The Rotterdam Study: 2016 objectives and design update
- HAIR LOSS IN WOMEN
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Dissecting the Molecular Mechanisms Involved in Keloid Pathogenesis and Response to Therapy
- Genetic Basis of Male Pattern Baldness
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Vitiligo
- Male fertility and skin diseases
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Side effects of sodium valproate during long-term treatment in epilepsy
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Intractable Diffuse Alopecia Caused by Multifactorial Side-Effects in Treatment of Acute Lymphocytic Leukemia: Connection to Iatrogenic Failure of Estrogen Secretion
- Formation of the cornified envelope
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Ectodermal Dysplasia: Variable Expressions