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Page 1
Upper lip abscess due to congenital sinus infection: A case report.
Imura H, Chimedtseren I, Furukawa H, Ito M, Natsume N. Imura H, et al. Among authors: furukawa h. Congenit Anom (Kyoto). 2022 May;62(3):134-135. doi: 10.1111/cga.12459. Epub 2022 Feb 17. Congenit Anom (Kyoto). 2022. PMID: 35137994 No abstract available.
Changes in the birth prevalence of orofacial clefts in Japan: Has the birth prevalence of orofacial clefts been affected by improved accuracy of prenatal diagnosis?
Natsume N, Furukawa H, Niimi T, Takeuchi K, Yoshida W, Sakuma C, Imura H, Fujiwara K, Akashi J, Hayami K, Natsume N. Natsume N, et al. Among authors: furukawa h. Congenit Anom (Kyoto). 2022 Jan;62(1):11-17. doi: 10.1111/cga.12444. Epub 2021 Sep 28. Congenit Anom (Kyoto). 2022. PMID: 34505318
Prevention of cleft lip and/or palate in A/J mice by licorice solution.
Chimedtseren I, Niimi T, Inoue M, Furukawa H, Imura H, Minami K, Garidkhuu A, Gantugs AE, Natsume N. Chimedtseren I, et al. Among authors: furukawa h. Congenit Anom (Kyoto). 2023 Sep;63(5):141-146. doi: 10.1111/cga.12527. Epub 2023 Jun 3. Congenit Anom (Kyoto). 2023. PMID: 37269175
Questionnaire survey on public awareness of cleft lip with/without palate in Mongolia.
Gantugs AE, Imura H, Chimedtseren I, Kitagawa K, Sakuma C, Natsume N, Kawana T, Badamnyambuu B, Kurose M, Niimi T, Furukawa H, Natsume N. Gantugs AE, et al. Among authors: furukawa h. Congenit Anom (Kyoto). 2024 Mar;64(2):40-46. doi: 10.1111/cga.12552. Epub 2024 Feb 3. Congenit Anom (Kyoto). 2024. PMID: 38308585
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.
Suzuki S, Marazita ML, Cooper ME, Miwa N, Hing A, Jugessur A, Natsume N, Shimozato K, Ohbayashi N, Suzuki Y, Niimi T, Minami K, Yamamoto M, Altannamar TJ, Erkhembaatar T, Furukawa H, Daack-Hirsch S, L'heureux J, Brandon CA, Weinberg SM, Neiswanger K, Deleyiannis FW, de Salamanca JE, Vieira AR, Lidral AC, Martin JF, Murray JC. Suzuki S, et al. Among authors: furukawa h. Am J Hum Genet. 2009 Mar;84(3):406-11. doi: 10.1016/j.ajhg.2009.02.002. Epub 2009 Feb 26. Am J Hum Genet. 2009. PMID: 19249007 Free PMC article.
Association between IRF6, TP63, GREM1 Gene Polymorphisms and Non-Syndromic Orofacial Cleft Phenotypes in Vietnamese Population: A Case-Control and Family-Based Study.
Pham LNG, Niimi T, Suzuki S, Nguyen MD, Nguyen LCH, Nguyen TD, Hoang KA, Nguyen DM, Sakuma C, Hayakawa T, Hiyori M, Natsume N, Furukawa H, Imura H, Akashi J, Ohta T, Natsume N. Pham LNG, et al. Among authors: furukawa h. Genes (Basel). 2023 Oct 25;14(11):1995. doi: 10.3390/genes14111995. Genes (Basel). 2023. PMID: 38002937 Free PMC article.
Two missense mutations in the IRF6 gene in two Japanese families with Van der Woude syndrome.
Matsuzawa N, Yoshiura K, Machida J, Nakamura T, Niimi T, Furukawa H, Toyoda T, Natsume N, Shimozato K, Niikawa N. Matsuzawa N, et al. Among authors: furukawa h. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004 Oct;98(4):414-7. doi: 10.1016/j.tripleo.2003.12.034. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004. PMID: 15472655
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
Butali A, Suzuki S, Cooper ME, Mansilla AM, Cuenco K, Leslie EJ, Suzuki Y, Niimi T, Yamamoto M, Ayanga G, Erkhembaatar T, Furukawa H, Fujiwawa K, Imura H, Petrin AL, Natsume N, Beaty TH, Marazita ML, Murray JC. Butali A, et al. Among authors: furukawa h. Am J Med Genet A. 2013 May;161A(5):965-72. doi: 10.1002/ajmg.a.35749. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463464 Free PMC article.