Gu XX - Search Results

1

Linkage analysis in three families with nonspecific X-linked mental retardation.

Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Claes S, et al. Among authors: gu xx. Am J Med Genet. 1996 Jul 12;64(1):137-46. doi: 10.1002/(SICI)1096-8628(19960712)64:1<137::AID-AJMG24>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826464

2

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Gu XX, Decorte R, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Gu XX, et al. J Med Genet. 1996 Jan;33(1):52-5. doi: 10.1136/jmg.33.1.52. J Med Genet. 1996. PMID: 8825049 Free PMC article.

3

Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DR beta 1 chain in multiple sclerosis.

Ghabanbasani MZ, Gu XX, Spaepen M, Vandevyver C, Raus J, Marynen P, Carton H, Cassiman JJ. Ghabanbasani MZ, et al. Among authors: gu xx. J Neuroimmunol. 1995 Jun;59(1-2):77-82. doi: 10.1016/0165-5728(95)00027-y. J Neuroimmunol. 1995. PMID: 7797622

4

Lack of association between HLA class II polymorphisms and essential hypertension in a Belgian population.

Gu XX, Spaepen M, Raeymaekers P, Guo C, Fagard R, Amery A, Lijnen P, Cassiman JJ. Gu XX, et al. J Hum Hypertens. 1995 Jul;9(7):553-5. J Hum Hypertens. 1995. PMID: 7562884

5

Lack of association between the I/D polymorphism of the angiotensin-converting enzyme gene and essential hypertension in a Belgian population.

Gu XX, Spaepen M, Guo C, Fagard R, Amery A, Lijnen P, Cassiman JJ. Gu XX, et al. J Hum Hypertens. 1994 Sep;8(9):683-5. J Hum Hypertens. 1994. PMID: 7807498

6

Genetic data obtained for two Chinese Han populations with a quadruplex fluorescent STR typing system (HUMVWA, HUMTH01, D21S11 and HPRT).

Xiao FX, Gilissen A, Gu XX, Cassiman JJ, Decorte R. Xiao FX, et al. Among authors: gu xx. Int J Legal Med. 1998;111(6):343-5. doi: 10.1007/s004140050187. Int J Legal Med. 1998. PMID: 9826100

7

Mutation analysis in adenylosuccinate lyase deficiency: eight novel mutations in the re-evaluated full ADSL coding sequence.

Marie S, Cuppens H, Heuterspreute M, Jaspers M, Tola EZ, Gu XX, Legius E, Vincent MF, Jaeken J, Cassiman JJ, Van den Berghe G. Marie S, et al. Among authors: gu xx. Hum Mutat. 1999;13(3):197-202. doi: 10.1002/(SICI)1098-1004(1999)13:3<197::AID-HUMU3>3.0.CO;2-D. Hum Mutat. 1999. PMID: 10090474

8

Association of particular HLA class II alleles, haplotypes and genotypes with susceptibility to IDDM in the Belgian population.

Buyse I, Sandkuyl LA, Zamani Ghabanbasani M, Gu XX, Bouillon R, Bex M, Dooms L, Emonds MP, Duhamel M, Marynen P, et al. Buyse I, et al. Among authors: gu xx. Diabetologia. 1994 Aug;37(8):808-17. doi: 10.1007/BF00404338. Diabetologia. 1994. PMID: 7988783 Clinical Trial.

9

HLA class II and T-cell receptor beta chain polymorphisms in Belgian patients with rheumatoid arthritis: no evidence for disease association with the TCRBC2, TCRBV8 and TCRBV11 polymorphisms.

Vandevyver C, Gu XX, Geusens P, Spaepen M, Philippaerts L, Cassiman JJ, Raus J. Vandevyver C, et al. Among authors: gu xx. Ann Rheum Dis. 1994 Sep;53(9):580-6. doi: 10.1136/ard.53.9.580. Ann Rheum Dis. 1994. PMID: 7979596 Free PMC article.

10

Association between miR-30 polymorphism and ischemic stroke in Chinese population.

Luo YP, Gu XX, Liu C, Huang Y, Lu LJ, Zhang SY, Yuan YL. Luo YP, et al. Among authors: gu xx. BMC Med Genomics. 2024 Nov 13;17(1):269. doi: 10.1186/s12920-024-02041-z. BMC Med Genomics. 2024. PMID: 39538152 Free PMC article.

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