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Research 211–240 of 1000+
- 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
- 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
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Design, Synthesis and Evaluation of N13-Substituted Evodiamine Derivatives against Human Cancer Cell Lines
- Multi-omics empowered deep phenotyping of ulcerative colitis
- Cronkhite-Canada Syndrome Associated With Superficial Esophageal Carcinoma: A Case Report and Literature Review
- 1446 RNase L acts as a regeneration suppressor
- Decision letter: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Actualités du SOPK