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Research 271–300 of 1000+
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Molecular Genetics of Alopecias
- Focal and Generalized Alopecia
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Disease causing homozygous variants in the human hairless gene
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Gene Therapy: Recent Advances and Applications in Dermatology
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Genetic prediction of male pattern baldness
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Genetic Defects of Female Sexual Differentiation
- Keratin disorders: from gene to therapy
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Molecular genetics of androgen insensitivity
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- What does acne genetics teach us about disease pathogenesis?
- The Genetics of Human Skin Disease
- Dermatopathology and molecular genetics
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Genetic Susceptibility to Alopecia
- Le gène<i>hairless</i>de la souris