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Research 91–120 of 247
- Aging and Anti-Aging in Hair and Hair Loss
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Assessment of the impact of VDR polymorphisms on selected hormonal, metabolic and mineral balance markers in young women with hyperandrogenism
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Actualités du SOPK
- Syndromes of Severe Insulin Resistance (SSIRs)
- Abstracts
- National scientific medical meeting 1996 abstracts
- Overexpression of mIGF-1 in Keratinocytes Improves Wound Healing and Accelerates Hair Follicle Formation and Cycling in Mice
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- Investigation of Paraoxanase Enzyme Polymorphism in Patients with Alopecia Areata
- SEXUAL DIMORPHISM IN MAMMALS
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Correction of ornithine transcarbamylase (OTC) deficiency in spf‐ash mice by introduction of rat OTC gene
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- The Mask Mutation Identifies TMPRSS6 as an Essential Suppressor of Hepcidin Gene Expression, Required for Normal Uptake of Dietary Iron.
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Pitfalls of PCR-Based Strategy for Genotyping <i>Cre-Loxp</i> Mice
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Alopecia areata
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