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    Research 151–180 of 1000+

    1. Superior Root Hair Formation Confers Root Efficiency in Some, But Not All, Rice Genotypes upon P Deficiency Frontiers in Plant Science · 2016 · 66 citations
    2. A.S.P.E.N. Parenteral Nutrition Trace Element Product Shortage Considerations Nutrition in Clinical Practice · 2014 · 14 citations
    3. DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma Frontiers in Cardiovascular Medicine · 2023 · 1 citations
    4. Dual blockage of P-cadherin and c-Met synergistically inhibits the growth of head and neck cancer Cellular Oncology · 2025
    5. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    6. <i>Bacillus subtilis</i> promotes plant phosphorus (P) acquisition through P solubilization and stimulation of root and root hair growth Physiologia Plantarum · 2024
    7. DENOUEMENT—CONTINUED FROM P. 661 The Pediatric Infectious Disease Journal · 2000
    8. Effects of in vivo-administered 2,3,7,8-tetrachlorodibenzo-p-dioxin on receptor binding of epidermal growth factor in the hepatic plasma membrane of rat, guinea pig, mouse, and hamster. Proceedings of the National Academy of Sciences · 1984 · 164 citations
    9. 2,3,7,8-Tetrachlorodibenzo-p-dioxin Increases the Expression of Genes in the Human Epidermal Differentiation Complex and Accelerates Epidermal Barrier Formation Toxicological sciences · 2011 · 86 citations
    10. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Affects Keratin 1 and Keratin 17 Gene Expression and Differentially Induces Keratinization in Hairless Mouse Skin Journal of Investigative Dermatology · 1997 · 45 citations
    11. An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome International Journal of Molecular Medicine · 2013 · 20 citations
    12. Preparation and Characterization of Solution-Processed Nanocrystalline p-Type CuAlO2 Thin-Film Transistors Nanoscale Research Letters · 2018 · 14 citations
    13. Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene Yonsei Medical Journal · 2018 · 13 citations
    14. Human placenta hydrolysates: from V.P. Filatov to the present day: Review Terapevticheskii arkhiv · 2022 · 9 citations
    15. Studies of the availability of soil phosphorus (P) and potassium (K) in organic farming systems, and of plant adaptations to low P- and K-availability Organic Eprints (International Centre for Research in Organic Food Systems, and Research Institute of Organic Agriculture) · 2003 · 9 citations
    16. Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome Endocrine journal · 2008 · 3 citations
    17. Bilateral facial nerve palsy associated with p-ANCA positive vasculitis in a patient with rheumatoid arthritis British Journal of Ophthalmology · 2001 · 3 citations
    18. Mycorrhiza-induced change in root hair growth is associated with IAA accumulation and expression of EXPs in trifoliate orange under two P levels Scientia Horticulturae · 2018 · 62 citations
    19. Comparison of Activities Dependent on Glutathione S-Transferase and Cytochrome P-450 IA1 in Cultured Keratinocytes and Reconstructed Epidermal Models Skin Pharmacology and Physiology · 2002 · 42 citations
    20. Characterization of spironolactone and metabolites derivatized using Girard's reagent P using mass spectrometry and ion mobility spectrometry Rapid Communications in Mass Spectrometry · 2024 · 4 citations
    21. A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome Diabetes Metabolic Syndrome and Obesity · 2024 · 1 citations
    22. Clinical and Laboratory Characteristics of Individuals Aged ≤17 Years With Homeostatic Iron Regulator (HFE) p.C282Y Homozygosity, a Common Hemochromatosis Genotype Curēus · 2023 · 1 citations
    23. Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother Archives of Endocrinology and Metabolism · 2024
    24. Evaluation of Hair Growth Promoting Activity of Sansevieria Trifasciata P. on Alopecia Androgenic Rabbit Male International journal of pharmaceutical research · 2021
    25. DEVELOPMENT OF HAIR TONIC COMPRISING A MIXED EXTRACT FROM FRUITS OF P. EMBLICA AND Z. LIMONELLA The Thai Journal of Pharmaceutical Sciences · 2013
    26. Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene Endocrine · 2011 · 8 citations
    27. Antialopecia Activity and IR-Spectrometry Characterization of Bioactive Compounds From Sansevieria trifasciata P. Egyptian Journal of Chemistry · 2022 · 5 citations
    28. Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year JCRPE · 2022 · 1 citations
    29. 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin Journal of Investigative Dermatology · 2023
    30. Clinical assessment and nutritional awareness among school going adolescent girls of Kanpur (U.P.) FOOD SCIENCE RESEARCH JOURNAL · 2019