Search
for
Sort by
Research 211–240 of 1000+
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- The diagnosis of polycystic ovary syndrome: the criteria are insufficiently robust for clinical research
- Redefining hormone resistance in prostate cancer
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Alterations in transcriptome and antioxidant activity of naturally aged mice exposed to selenium-rich rice
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- The Use of Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryos during Organogenesis and Their Role in Regulating the Gene Expression of Normal and Pathological (Stem) Cells
- The Hidden Link between Polycystic Ovary Syndrome and Kidney Stones: Finding from the Tehran Lipid and Glucose Study (TLGS)
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- <i>WNT10A</i> , dermatology and dentistry
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Ottawa, Ontario, Canada, February 13–16, 2013
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Comparison of two ASC-derived therapeutics in an in vitro OA model: secretome versus extracellular vesicles
- Approach to androgen excess in women: Clinical and biochemical insights
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Diagnostic approach to low‐renin hypertension
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- Evaluating the diagnostic accuracy of androgen measurement in polycystic ovary syndrome: a systematic review and diagnostic meta-analysis to inform evidence-based guidelines
- Criteria for Defining Polycystic Ovary Syndrome as a Predominantly Hyperandrogenic Syndrome: An Androgen Excess Society Guideline