PubMed for id: 162922

Year	Number of Results
1988	1
1991	1
1992	1
1993	1
1994	2
1996	2
2001	1
2019	1
2020	2
2021	142
2022	191
2023	176
2024	56

1

[X-linked recessive chondrodysplasia punctata. Cytogenetic study and role of molecular biology].

Malou E, Gekas J, Troucelier-Lucas V, Mornet E, Razafimanantsoa L, Cuvelier B, Mathieu M, Thépot F. Malou E, et al. Arch Pediatr. 2001 Feb;8(2):176-80. doi: 10.1016/s0929-693x(00)00181-0. Arch Pediatr. 2001. PMID: 11232459 French.

2

Regional localisation of two non-specific X-linked mental retardation genes (MRX30 and MRX31).

Donnelly AJ, Partington MW, Ryan AK, Mulley JC. Donnelly AJ, et al. Am J Med Genet. 1996 Jul 12;64(1):113-20. doi: 10.1002/(SICI)1096-8628(19960712)64:1<113::AID-AJMG19>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8826460

3

Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38).

Schutz CK, Ives EJ, Chalifoux M, MacLaren L, Farrell S, Robinson PD, White BN, Holden JJ. Schutz CK, et al. Am J Med Genet. 1996 Jul 12;64(1):89-96. doi: 10.1002/(SICI)1096-8628(19960712)64:1<89::AID-AJMG16>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8826457

4

Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.

Kozák L, Chiurazzi P, Genuardi M, Pomponi MG, Zollino M, Neri G. Kozák L, et al. J Med Genet. 1993 Oct;30(10):866-9. doi: 10.1136/jmg.30.10.866. J Med Genet. 1993. PMID: 8230164 Free PMC article.

5

Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.

Hu LJ, Blumenfeld-Heyberger S, Hanauer A, Weissenbach J, Mandel JL. Hu LJ, et al. Am J Med Genet. 1994 Jul 15;51(4):569-74. doi: 10.1002/ajmg.1320510455. Am J Med Genet. 1994. PMID: 7943041

6

Pericentromeric genes for non-specific X-linked mental retardation (MRX).

Gedeon A, Kerr B, Mulley J, Turner G. Gedeon A, et al. Am J Med Genet. 1994 Jul 15;51(4):553-64. doi: 10.1002/ajmg.1320510453. Am J Med Genet. 1994. PMID: 7943039

7

Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2).

Sutherland GR, Gedeon AK, Haan EA, Woodroffe P, Mulley JC. Sutherland GR, et al. Am J Med Genet. 1988 May-Jun;30(1-2):493-508. doi: 10.1002/ajmg.1320300152. Am J Med Genet. 1988. PMID: 3177467

8

Localisation of the MRX3 gene for non-specific X linked mental retardation.

Gedeon A, Kerr B, Mulley J, Turner G. Gedeon A, et al. J Med Genet. 1991 Jun;28(6):372-7. doi: 10.1136/jmg.28.6.372. J Med Genet. 1991. PMID: 1870093 Free PMC article.

9

Nomenclature guidelines for X-linked mental retardation.

Mulley JC, Kerr B, Stevenson R, Lubs H. Mulley JC, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):383-91. doi: 10.1002/ajmg.1320430159. Am J Med Genet. 1992. PMID: 1605216 Review.

10

SigH stress response mediates killing of Mycobacterium tuberculosis by activating nitronaphthofuran prodrugs via induction of Mrx2 expression.

Cioetto-Mazzabò L, Boldrin F, Beauvineau C, Speth M, Marina A, Namouchi A, Segafreddo G, Cimino M, Favre-Rochex S, Balasingham S, Trastoy B, Munier-Lehmann H, Griffiths G, Gicquel B, Guerin ME, Manganelli R, Alonso-Rodríguez N. Cioetto-Mazzabò L, et al. Nucleic Acids Res. 2023 Jan 11;51(1):144-165. doi: 10.1093/nar/gkac1173. Nucleic Acids Res. 2023. PMID: 36546765 Free PMC article.

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