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Research 331–360 of 1000+
- Sex-specific Difference of Hippocampal Synaptic Plasticity in Response to Sex Neurosteroids
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Exploring climate adaptation in European Merino sheep: a landscape genomics approach
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- New familial association between ocular coloboma and loose anagen syndrome
- Human Derived Immortalized Dermal Papilla Cells With a Constant Expression of Testosterone Receptor
- Nosocomial Intravascular Catheter Infections with Extended-spectrum Beta-lactamase-producing<i>Escherichia coli</i>in Calves after Strain Introduction from a Commercial Herd
- Comment on: The Gabrin sign
- Index of Suspicion
- Clinical Corner: Case Report Spermatozoa and Chronic Treatment with Finasteride: A TEM and FISH Study
- 4th Intercontinental Meeting of Hair Research Societies 2004 The "World of Hair"
- Depression from a physical symptom.
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Rheumatoid arthritis and gouty arthritis in an adult patient with Down's syndrome
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Congenital Adrenal Hyperplasia
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- 5-Alpha reductase deficiency
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- 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
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia