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Research 841–870 of 1000+
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII
- Abstract C4: Sp2: A regulator of stem cell differentiation and tumorigenesis
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b
- Non-Edg family LPA receptors: the cutting edge of LPA research
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Identification of genes influencing formation of the Type III Brush Hair in Yangtze River Delta white goats by differential display of mRNA
- Neurochemical and Immunocytochemical Studies of Catecholamine System in the Brindled Mouse
- Endocrine systems of the skin
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene
- The parathyroid hormone-related protein as a regulator of normal tissue functions
- An Overview on Functional and Structural Properties of Monomeric and Multimeric β-Thymosin in Invertebrates
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- The Expression of P-Responsive Genes is Related to Root Hair Growth
- Generation of a Novel Inducible and Dermal Papilla‐Specific <i>Wif1‐CreER</i> Knock‐In Mouse Line for Hair Follicle Research
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Faculty Opinions recommendation of The Venus flytrap trigger hair-specific potassium channel KDM1 can reestablish the K+ gradient required for hapto-electric signaling.
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Function of KLF4 in Stem Cell Biology
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Progeroide Syndrome
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia