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Research 331–360 of 605
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 874 Chromatin architectural protein CTCF controls epidermal barrier formation, hair follicle fate maintenance and suppresses inflammatory responses in the skin epithelium
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- 14 Rhytidectomy
- Modelling androgen synthesis and action during human sexual differentiation
- 14. Wound Healing; Cutaneous Therapy; Hair
- Syndromes of Severe Insulin Resistance (SSIRs)
- Cutaneous signals of immune system disease
- STUDIED ON TOXICITY OF HYDROCORTISONE 17-BUTYRATE 21-PROPIONATE : 6. Subacute Toxicity in Dogs by Percutaneous Adminisration
- Prevalence of polycystic ovary syndrome in women in China: a large community-based study
- Tributyltin (TBT) effects on Ocinebrina aciculata (Gastropoda: Muricidae): imposex development, sterilization, sex change and population decline
- Group IID, IIE, IIF and III secreted phospholipase A2s
- <i>Zizyphus jujuba</i>protects against ibuprofen-induced nephrotoxicity in rats
- A Comprehensive Review on Phytochemistry and Pharmacological Effects of Stinging Nettle (Urtica dioica)
- PCOS and Obesity: Contraception Challenges
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Combined oral contraceptives promote androgen receptor and oestrogen receptor alpha upregulation in the female prostate (Skene’s paraurethral glands) of adult gerbils (Meriones unguiculatus)
- AVALIAÇÃO DO USO DE TELAS DIGITAIS POR CRIANÇAS E ADOLESCENTES EM TEMPOS DE PANDEMIA
- Immunoglobulin E and Serum Interleukin-13 and Bacteria in Patients with Alopecia Areata
- Dermal EZH2 simultaneously orchestrates dermal differentiation and epidermal proliferation during murine skin development
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Activation of Polyamine Catabolism Profoundly Alters Tissue Polyamine Pools and Affects Hair Growth and Female Fertility in Transgenic Mice Overexpressing Spermidine/SpermineN 1-Acetyltransferase
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Zinc Deficiency in Suckling Mice Deprived of Colostrum
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- Diffuse scalp hair loss due to levothyroxine overdose