Search
for
Sort by
Research 931–960 of 1000+
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Past, Present and Future Perspectives of Forensic Genetics
- De novo assembly and annotation of Asiatic lion (<i>Panthera leo persica</i>) genome
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology
- The First Visit: Consult and Workup Before Sperm Banking
- Abstract 5202: Bone marrow-derived epithelial cells contribute to chronic skin inflammation and skin tumor formation in the mouse
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Androgen biosynthetic pathways in the human prostate
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Development of Heritable Melanoma in Transgenic Mice
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- <i>Saccharomyces cerevisiae</i> BLYAS, a New Bioluminescent Bioreporter for Detection of Androgenic Compounds
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Heterogeneous Stem Cells in Skin Homeostatis and Wound Repair
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Characterization and expression analysis of KAP7.1, KAP8.2 gene in Liaoning new-breeding cashmere goat hair follicle
- Hormonal Therapies for Individuals with Intersex Conditions
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia