PubMed for id: 300797028

Year	Number of Results
1993	2
1995	1
1997	1
1998	2
2004	1
2009	1
2018	1
2023	3
2024	2

1

Erdr1 Drives Macrophage Programming via Dynamic Interplay with YAP1 and Mid1.

Wang Y. Wang Y. Immunohorizons. 2024 Feb 1;8(2):198-213. doi: 10.4049/immunohorizons.2400004. Immunohorizons. 2024. PMID: 38392560 Free PMC article.

2

Absence of the RING domain in MID1 results in patterning defects in the developing human brain.

Frank S, Gabassi E, Käseberg S, Bertin M, Zografidou L, Pfeiffer D, Brennenstuhl H, Falk S, Karow M, Schweiger S. Frank S, et al. Life Sci Alliance. 2024 Jan 18;7(4):e202302288. doi: 10.26508/lsa.202302288. Print 2024 Apr. Life Sci Alliance. 2024. PMID: 38238086 Free PMC article.

3

Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant.

Perea-Cabrera M, Granados-Riveron JT, Segura-Stanford B, Moreno-Vargas LM, Prada-Gracia D, Moran-Espinosa MC, Erdmenger J, Diaz-Garcia H, Sánchez-Urbina R. Perea-Cabrera M, et al. Mol Genet Genomic Med. 2023 Sep;11(9):e2234. doi: 10.1002/mgg3.2234. Epub 2023 Jul 27. Mol Genet Genomic Med. 2023. PMID: 37498300 Free PMC article.

4

B-box1 Domain of MID1 Interacts with the Ube2D1 E2 Enzyme Differently Than RING E3 Ligases.

Kaur A, Gladu EM, Wright KM, Webb JA, Massiah MA. Kaur A, et al. Biochemistry. 2023 Mar 7;62(5):1012-1025. doi: 10.1021/acs.biochem.2c00693. Epub 2023 Feb 23. Biochemistry. 2023. PMID: 36820504

5

Esophageal Atresia / Tracheoesophageal Fistula Overview – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.

Scott DA. Scott DA. 2009 Mar 12 [updated 2018 Sep 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2009 Mar 12 [updated 2018 Sep 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301753 Free Books & Documents. Review.

6

MID1-Related Opitz G/BBB Syndrome.

Meroni G. Meroni G. 2004 Dec 17 [updated 2023 Oct 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2004 Dec 17 [updated 2023 Oct 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301502 Free Books & Documents. Review.

7

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain.

Gaudenz K, Roessler E, Quaderi N, Franco B, Feldman G, Gasser DL, Wittwer B, Horst J, Montini E, Opitz JM, Ballabio A, Muenke M. Gaudenz K, et al. Am J Hum Genet. 1998 Sep;63(3):703-10. doi: 10.1086/302010. Am J Hum Genet. 1998. PMID: 9718340 Free PMC article.

8

The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome.

Perry J, Feather S, Smith A, Palmer S, Ashworth A. Perry J, et al. Hum Mol Genet. 1998 Feb;7(2):299-305. doi: 10.1093/hmg/7.2.299. Hum Mol Genet. 1998. PMID: 9425238

9

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.

Quaderi NA, Schweiger S, Gaudenz K, Franco B, Rugarli EI, Berger W, Feldman GJ, Volta M, Andolfi G, Gilgenkrantz S, Marion RW, Hennekam RC, Opitz JM, Muenke M, Ropers HH, Ballabio A. Quaderi NA, et al. Nat Genet. 1997 Nov;17(3):285-91. doi: 10.1038/ng1197-285. Nat Genet. 1997. PMID: 9354791 Free article.

10

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.

Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R, Leonard CO, Burton BK, Josephson KD, Laxová R, Aleck KA, Allanson JE, Guion-Almeida ML, Martin RA, Leichtman LG, Price RA, Opitz JM, Muenke M. Robin NH, et al. Nat Genet. 1995 Dec;11(4):459-61. doi: 10.1038/ng1295-459. Nat Genet. 1995. PMID: 7493033

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