PubMed for id: 373141

Year	Number of Results
1989	1
1997	1
1998	2
1999	1
2000	1
2002	1
2003	1
2004	1
2005	2
2006	2
2008	1
2009	5
2010	5
2011	3
2012	4
2013	2
2014	1
2016	4
2017	2
2018	3
2019	3
2020	2
2021	3
2022	1
2023	3
2024	1

1

Cloning of two Bombyx homologues of the Drosophila rosy gene and their relationship to larval translucent skin colour mutants.

Yasukochi Y, Kanda T, Tamura T. Yasukochi Y, et al. Genet Res. 1998 Feb;71(1):11-9. doi: 10.1017/s0016672397003078. Genet Res. 1998. PMID: 9674379

2

Functional characterization of Bmcap in uric acid metabolism in the silkworm.

Tang L, Yang D, Liu Z, Wang Y, Yang X, Liu Y, Chen D, Tang Z, Huang Y. Tang L, et al. Insect Sci. 2024 Feb;31(1):147-156. doi: 10.1111/1744-7917.13236. Epub 2023 Jun 26. Insect Sci. 2024. PMID: 37358054

3

Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review.

Gavril EC, Nucă I, Pânzaru MC, Ivanov AV, Mihai CT, Antoci LM, Ciobanu CG, Rusu C, Popescu R. Gavril EC, et al. Genes (Basel). 2023 Feb 11;14(2):465. doi: 10.3390/genes14020465. Genes (Basel). 2023. PMID: 36833393 Free PMC article. Review.

4

Relationship between phenotypic features in Loeys-Dietz syndrome and the presence of intracranial aneurysms.

Huguenard AL, Johnson GW, Desai RR, Osbun JW, Dacey RG, Braverman AC. Huguenard AL, et al. J Neurosurg. 2022 Oct 28;138(5):1385-1392. doi: 10.3171/2022.9.JNS221373. Print 2023 May 1. J Neurosurg. 2022. PMID: 36308480

5

Loeys-Dietz Syndrome.

Velchev JD, Van Laer L, Luyckx I, Dietz H, Loeys B. Velchev JD, et al. Adv Exp Med Biol. 2021;1348:251-264. doi: 10.1007/978-3-030-80614-9_11. Adv Exp Med Biol. 2021. PMID: 34807423

6

5'-Nucleotidase Plays a Key Role in Uric Acid Metabolism of Bombyx mori.

Tang L, Yang D, Wang Y, Yang X, Chen K, Luo X, Xu J, Liu Y, Tang Z, Zhang Q, Liu Z, Huang Y. Tang L, et al. Cells. 2021 Aug 30;10(9):2243. doi: 10.3390/cells10092243. Cells. 2021. PMID: 34571893 Free PMC article.

7

Ehlers-Danlos Syndrome Type IV - Anaesthetic Considerations.

Kazakov D, Pavlov G, Stefanov C. Kazakov D, et al. Folia Med (Plovdiv). 2021 Feb 28;63(1):153-155. doi: 10.3897/folmed.63.e53968. Folia Med (Plovdiv). 2021. PMID: 33650410

8

Biallelic variants in EFEMP1 in a man with a pronounced connective tissue phenotype.

Driver SGW, Jackson MR, Richter K, Tomlinson P, Brockway B, Halliday BJ, Markie DM, Robertson SP, Wade EM. Driver SGW, et al. Eur J Hum Genet. 2020 Apr;28(4):445-452. doi: 10.1038/s41431-019-0546-7. Epub 2019 Dec 2. Eur J Hum Genet. 2020. PMID: 31792352 Free PMC article.

9

A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis.

Shalhub S, Byers PH, Hicks KL, Coleman DM, Davis FM, De Caridi G, Weaver KN, Miller EM, Schermerhorn ML, Shean K, Oderich G, Ribeiro M, Nishikawa C, Charlton-Ouw K, Behrendt CA, Debus ES, von Kodolitsch Y, Zarkowsky D, Powell RJ, Pepin M, Milewicz DM, Regalado ES, Lawrence PF, Woo K. Shalhub S, et al. J Vasc Surg. 2020 Jan;71(1):149-157. doi: 10.1016/j.jvs.2019.04.487. Epub 2019 Jul 26. J Vasc Surg. 2020. PMID: 31353273 Free PMC article.

10

SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy.

Fischer-Zirnsak B, Koenig R, Alisch F, Güneş N, Hausser I, Saha N, Beck-Woedl S, Haack TB, Thiel C, Kamrath C, Tüysüz B, Henning S, Mundlos S, Hoffmann K, Horn D, Kornak U. Fischer-Zirnsak B, et al. J Hum Genet. 2019 Jul;64(7):609-616. doi: 10.1038/s10038-019-0602-8. Epub 2019 Apr 24. J Hum Genet. 2019. PMID: 31015584

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