Hosomichi K.
30
Coauthors
7
Documentos
Volumen de publicaciones por año
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| Año de publicación | Num. Publicaciones |
|---|---|
| 2017 | 1 |
| 2018 | 1 |
| 2020 | 1 |
| 2021 | 1 |
| 2022 | 2 |
| 2023 | 1 |
Publicaciones por áreas de conocimiento
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| Área de conocimiento | Num. Publicaciones |
|---|---|
| Genética | 9 |
| Evolución | 2 |
| Cáncer | 2 |
Publicaciones por áreas temáticas
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| Área temática | Num. Publicaciones |
|---|---|
| Enfermedades | 5 |
| Fisiología humana | 3 |
| Mammalia | 2 |
| Ginecología, obstetricia, pediatría, geriatría | 1 |
| Sistemas fisiológicos específicos de los animales | 1 |
| Bioquímica | 1 |
Principales fuentes de datos
| Origen | Num. Publicaciones |
|---|---|
| Scopus | 7 |
| Google Scholar | 3 |
| RRAAE | 0 |
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Coautores destacados por número de publicaciones
| Coautor | Num. Publicaciones |
|---|---|
| Vanessa Romero | 7 |
| Nakaoka H. | 2 |
| Inoue I. | 2 |
| Reyes C. | 2 |
| Benjamín Arias-Almeida | 2 |
| Liehr T. | 1 |
| Juan Carlos Pozo-Palacios | 1 |
| Arianne Llamos Paneque | 1 |
| Samantha Sáenz Hinojosa | 1 |
| Tajima A. | 1 |
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Publicaciones del autor
High order formation and evolution of hornerin in primates
ArticleAbstract: Genomic duplication or loss can accelerate evolution because the number of repeats could affect molePalabras claves:Birth-and-death model, Epidermal differentiation complex, Hornerin, HRNR, Primate, S100 fused type proteinAutores:Hosomichi K., Inoue I., Nakaoka H., Vanessa RomeroFuentes:googlescopusThe limits of clinical findings in similar phenotypes, from Carpenter to ATRX syndrome using a whole exome sequencing approach: a case review
ReviewAbstract: Background: The diagnostic process for uncommon disorders with similar manifestations is complicatedPalabras claves:ATRX syndrome, Rare Diseases, Whole exome sequencingAutores:Arias B., Hosomichi K., Samantha S. Sáenz, Vanessa RomeroFuentes:scopusNovel SRY-box transcription factor 9 variant in campomelic dysplasia and the location of missense and nonsense variants along the protein domains: A case report
ArticleAbstract: Background: Campomelic dysplasia (CD) is a rare disorder that involves the skeletal and genital systPalabras claves:campomelic dysplasia, ECUADOR, high-mobility group box (HMG), self-dimerization domain (DIM), SOX9 geneAutores:Carlos A. Calvache, Estefanía C. Vásquez, Hosomichi K., Juan C. Pozo, Vanessa RomeroFuentes:scopusStructure and evolution of the filaggrin gene repeated region in primates
ArticleAbstract: Background: The evolutionary dynamics of repeat sequences is quite complex, with some duplicates nevPalabras claves:Birth-and-death evolution, copy number variation, Duplication/loss, FilaggrinAutores:Hosomichi K., Inoue I., Nakaoka H., Shibata H., Vanessa RomeroFuentes:googlescopusNovel Variation in Acyl-CoA Synthetase Long Chain Family Member 6 (ACSL6) Results in Protein Structural Modification and Multiple Non-Related Neoplasia in a 46-Year-Old: Case Report
ArticleAbstract: Multiple non-related neoplasia does not have an established approach or benefits for performing wholPalabras claves:ACSL6, astrocytoma, Breast, missense, thyroidAutores:Benjamín Arias-Almeida, Erick Freire, Hosomichi K., María Isabel Castillo, Reyes C., Vanessa RomeroFuentes:scopus