valine
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Research 10
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- 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>)
- Prevalence of nutritional deficiencies in hair loss among Indian participants: Results of a cross-sectional study
- A mutation in MAP2 is associated with prenatal hair follicle density
- THE N- AND C-TERMINAL END GROUPS OF HAIR KERATIN
- Comparative studies of hair shaft components between healthy and diseased donors
- Identification of VLDL as a biomarker for prewarning of androgenic alopecia
- Acrodermatitis Dysmetabolica with Concomitant Acquired Acrodermatitis Enteropathica in a Patient with Maple Syrup Urine Disease
- Amino Acids Oral Treatment for the Amelioration of Skin, Hair, and Nails Conditions: An Open-Label Study
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications