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Research 721–750 of 1000+
- Wound Induced Hair Neogenesis – A Novel Paradigm for Studying Regeneration and Aging
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Dermatopathology and molecular genetics
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Lentivirus-Mediated Expression of VEGF165 in Rat Hair Follicle Stem Cells
- Lrig1 Expression in Human Sebaceous Gland Tumors
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Perforins Expression by Cutaneous Gamma Delta T Cells
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Keratin gene mutations in disorders of human skin and its appendages
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Lrig1-expression confers suppressive function to CD4+ cells and is essential for averting autoimmunity via the Smad2/3/Foxp3 axis
- Increased CRHR1 expression on monocytes from patients with AA enables a pro‐inflammatory response to corticotrophin‐releasing hormone
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix