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Research 451–480 of 823
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Unknown safety profile of ingredients in hair supplements: A call to action for improved patient safety
- Skin Organogenesis and Dysmorphogenetic Factors in Skin Diseases (Review)
- Function-driven geometry directs human pilosebaceous unit development
- Fetal gender: preferences, predictions, and its impact on women's sexuality, physical activity, and well-being during pregnancy
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- Role of Androgen Receptor in Hypothalamic Regulation of Metabolism and Reproduction
- Management of pregnancy in a carrier of the Donohue mutation
- Pharmaceutical care in the use of vitamin-mineral complexes for women during pregnancy and lactation
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: Use of the method for analysis of keratins and filaggrin
- Histological changes of pre and postnatal Skin Development in Rats
- Morphogenesis of Mammary Glands in Buffalo (<i>Bubalus bubalis</i>)
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Cardiac Outflow tract septation defects in a DiGeorge syndrome model respond to Minoxidil treatment.
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- DETERMINANTS ELEMENTS OF ANEMIA IN PREGNANT WOMEN CONSULTING IN HEALTH CARE STRUCTURE OF CASABLANCA AND SAFI
- In utero Diagnosis of Trichothiodystrophy by Endoscopically-Guided Fetal Eyebrow Biopsy
- Chemical Structure, Classification and Clinical Significance of Steroid Hormones: A Review Article
- Neurotrophins, nociceptors, and pain
- Testosterone and the Brain: From Cognition to Autism
- US Preterm Births: “D” Is for Dismal
- Two parietal cephaloceles in a female neonate
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- Genetic hair and nail disorders
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Management of CAH during pregnancy
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium