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Research 811–840 of 825
- NEONATAL INHIBITION OF ANDROGEN ACTIVITY ALTERS THE PROGRAMMING OF BODY WEIGHT AND OREXINERGIC PEPTIDES DIFFERENTIALLY IN MALE AND FEMALE RATS
- Effects of Dietary Selenium Yeast Supplementation in Pregnant Cashmere Goats on the Development of Offspring Hair Follicles
- The Effects of Environmental Pollutants and Exposures on Hair Follicle Pathophysiology
- Advances in mitochondria-centered mechanism behind the roles of androgens and androgen receptor in the regulation of glucose and lipid metabolism
- Efficacy of an Oral Ageratum Conyzoides Formulation on Increasing Hair Growth and Decreasing Hair Loss in Males and Females: A Randomised Double-Blind Placebo-Controlled Study
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Author response: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Effect of zinc, ferritin, and vitamin B12 deficiency on hair loss in pregnant women
- Decision letter: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- What do we need to know about hair straightening?
- The Relationship of the 2nd: 4th Digit Ratio to the Maxillary Sinus Volume in Men
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- Transient treatment of pregnant Merino ewes with modulators of cortisol biosynthesis coinciding with primary wool follicle initiation alters lifetime wool growth
- Integrated analysis of miRNAs and mRNA profiling reveals the potential roles of miRNAs in sheep hair follicle development
- MiR-23b and miR-133 Cotarget TGFβ2/NOTCH1 in Sheep Dermal Fibroblasts, Affecting Hair Follicle Development
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q
- Prenatal serological diagnosis of intrauterine cytomegalovirus infection.
- Prenatal Screening for Bathing-suit Ichthyosis After Diagnosis in an Older Sibling
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis
- PCOS: update and diagnostic approach
- Inherited ichthyosis: Syndromic forms
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- Management of pregnancy in a carrier of the Donohue mutation
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Síndrome de ovario poliquístico: la distancia anogenital como marcador del entorno androgénico prenatal y revisión y comparación de los criterios diagnósticos