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Research 61–90 of 98
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- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- TONGUE, RED
- Valproic acid. A reappraisal of its pharmacological properties and clinical efficacy in epilepsy.
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Therapeutic, Prophylactic, and Functional Use of Probiotics: A Current Perspective
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Palatogenesis and cutaneous repair: A two‐headed coin
- A Nano-Pharmaceutical Formula of Quercetin Protects from Cardiovascular Complications Associated with Metabolic Syndrome
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Identification of xenobiotics interfering with 5 <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" id="d1e152" altimg="si21.svg"> <mml:mi>α</mml:mi> </mml:math> -reductase (SRD5A2) activity
- Feminization Surgery of the Upper Face as the Crucial Factor in Gender Confirmation—Pearls and Pitfalls
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Frizzled Receptors in Development and Disease
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Association between lower hair zinc levels and Neural Tube Defects
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- FOXN1 deficient nude severe combined immunodeficiency
- Clinical review of ejaculatory dysfunction
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Protein degradation: expanding the toolbox to restrain cancer drug resistance
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity