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Research 661–690 of 798
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Molecular Genetics of Alopecias
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Synchronizing actin and microtubules for axonal branching
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- 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
- Expression and Distribution of the Guanine Nucleotide-binding Protein Subunit Alpha-s in Mice Skin Tissues and Its Association with White and Black Coat Colors
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Congenital Atrichia: A Case Report
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- WNT10B (wingless-type MMTV integration site family)
- A Case of Azathioprine Induced Severe Myelosuppression and Alopecia Totalis in IgA Nephropathy
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Watching hair grow
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Monilethrix Treated with Minoxidil
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma