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Research 181–210 of 1000+
- From Hair to Colon: Hair Follicle-Derived MSCs Alleviate Pyroptosis in DSS-Induced Ulcerative Colitis by Releasing Exosomes in a Paracrine Manner
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Septin4 promotes cell death in human colon cancer cells by interacting with BAX
- Delayed Diagnosis of Familial Adenomatous Polyposis-related Colon Cancer in an Adolescent with Coexisting Eating Disorder: A Case Report
- Colonic Intussusception due to a Large Ascending Colon Lipoma
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Fatal Toxic Epidermal Necrolysis Associated With Cetuximab in a Patient With Colon Cancer
- METTL1-mediated m7G tRNA modification drives papillary thyroid cancer progression and metastasis by regulating the codon-specific translation of TNF-α
- Results of Open-Label non-Randomized Comparative Clinical Trial: “BromhexIne and Spironolactone for CoronаvirUs Infection requiring hospiTalization (BISCUIT)
- Effects of Rosmarinus officinalis extract on wound healing, colon anastomosis, and postoperative adhesion in colon anastomosis rats
- EVALUATE THE SAFETY AND EFFICACY OF LAPAROSCOPIC RESECTION VS OPEN SURGERY FOR THE CURATIVE CARE OF PATIENTS HAVING TUMORS OF THE RIGHT OR LEFT COLON
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Non-Contraceptive Benefits of Oral Hormonal Contraceptives
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Male pattern baldness and risk of colorectal neoplasia
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Anti-androgenic potential of the fruit extracts of certain Egyptian <i>Sabal</i> species and their genetic variability studies: a metabolomic-molecular modeling approach
- Isolation and characterization of a sheep cysteine-rich cuticle keratin pseudogene
- XX/XY chimerism in tortoiseshell tomcats – a new case and review of the literature
- MICRO-URZĄDZENIA, BEZPRZEWODOWE KAPSUŁKI, MAPY, STYMULATORY I ROZRUSZNIKI STOSOWANE DO DIAGNOSTYKI I LECZENIA ZABURZEŃ MOTORYKI PRZEWODU POKARMOWEGO
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
- 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