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Research 451–480 of 1000+
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Melanosis Coli After Long-Term Ingestion of Cape Aloe
- Management of adverse events and other practical considerations in patients receiving capecitabine (Xeloda®)
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome
- Reglering av keratiner i tjocktarmens epitelceller vid inflammatorisk signalering
- Caractérisation d’une modification «bigarré» de la couleur du pelage chez le chat domestique
- In-vitro and In-vivo Characterization of Gold Nanoparticles for the Treating of Inflammatory Bowel Disease
- Uji Aktivitas Sitotoksik Ekstrak Etanol dan Metanol Spirulina platensis L. terhadap Sel WiDr
- Functional analysis of collagen XVII in epithelial cancers and a mouse model
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Effective holistic characterization of small molecule effects using heterogeneous biological networks
- Hypertrichosis, trichomegaly, and androgenic alopecia related to cetuximab treatment
- UNUSUAL PRESENTATION OF LUPUS ENTERITIS WITH COLORECTAL INVOLVEMENT: A RARE CASE REPORT IN BANGLADESH
- Editor's evaluation: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- "A literature review on “Triphala’s Rasayana Karmukata."
- "A literature review on “Triphala’s Rasayana Karmukata."
- Abstract 5022: Keratin15 (Krt15) + are radio resistant and tumor-initiating cells in the mouse small intestine
- A Rare Case of Cronkhite-Canada Syndrome
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- Freeze‐Drying Tumor Tissues Derived Bio‐Patches With Hair Melanin Nanoparticles Integration for Wound Healing
- Increased Expression of TSPEAR in Colorectal Cancer Predicts Poor Prognosis
- Increased Expression of TSPEAR in Colorectal Cancer Predicts Poor Prognosis
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor