van Heyningen V - Search Results

1

Hanson IM, Seawright A, Hardman K, Hodgson S, Zaletayev D, Fekete G, van Heyningen V. Hanson IM, et al. Among authors: van heyningen v. Hum Mol Genet. 1993 Jul;2(7):915-20. doi: 10.1093/hmg/2.7.915. Hum Mol Genet. 1993. PMID: 8364574

2

Human RAG2, like RAG1, is on chromosome 11 band p13 and therefore not linked to ataxia telangiectasia complementation groups.

Sherrington PD, Forster A, Seawright A, van Heyningen V, Rabbitts TH. Sherrington PD, et al. Among authors: van heyningen v. Genes Chromosomes Cancer. 1992 Nov;5(4):404-6. doi: 10.1002/gcc.2870050417. Genes Chromosomes Cancer. 1992. PMID: 1283330

3

The human PAX6 gene is mutated in two patients with aniridia.

Jordan T, Hanson I, Zaletayev D, Hodgson S, Prosser J, Seawright A, Hastie N, van Heyningen V. Jordan T, et al. Among authors: van heyningen v. Nat Genet. 1992 Aug;1(5):328-32. doi: 10.1038/ng0892-328. Nat Genet. 1992. PMID: 1302030

4

Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.

Little MH, Dunn R, Byrne JA, Seawright A, Smith PJ, Pritchard-Jones K, van Heyningen V, Hastie ND. Little MH, et al. Among authors: van heyningen v. Oncogene. 1992 Apr;7(4):635-41. Oncogene. 1992. PMID: 1314367

5

Zinc finger point mutations within the WT1 gene in Wilms tumor patients.

Little MH, Prosser J, Condie A, Smith PJ, Van Heyningen V, Hastie ND. Little MH, et al. Among authors: van heyningen v. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4791-5. doi: 10.1073/pnas.89.11.4791. Proc Natl Acad Sci U S A. 1992. PMID: 1317572 Free PMC article.

6

Modulation of DNA binding specificity by alternative splicing of the Wilms tumor wt1 gene transcript.

Bickmore WA, Oghene K, Little MH, Seawright A, van Heyningen V, Hastie ND. Bickmore WA, et al. Among authors: van heyningen v. Science. 1992 Jul 10;257(5067):235-7. doi: 10.1126/science.1321494. Science. 1992. PMID: 1321494

7

Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.

Fantes JA, Bickmore WA, Fletcher JM, Ballesta F, Hanson IM, van Heyningen V. Fantes JA, et al. Among authors: van heyningen v. Am J Hum Genet. 1992 Dec;51(6):1286-94. Am J Hum Genet. 1992. PMID: 1334370 Free PMC article.

8

Mouse Small eye results from mutations in a paired-like homeobox-containing gene.

Hill RE, Favor J, Hogan BL, Ton CC, Saunders GF, Hanson IM, Prosser J, Jordan T, Hastie ND, van Heyningen V. Hill RE, et al. Among authors: van heyningen v. Nature. 1992 Feb 20;355(6362):750. doi: 10.1038/355750a0. Nature. 1992. PMID: 1346927 No abstract available.

9

The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13-p14.

Hanson IM, Seawright A, van Heyningen V. Hanson IM, et al. Among authors: van heyningen v. Genomics. 1992 Aug;13(4):1331-3. doi: 10.1016/0888-7543(92)90060-6. Genomics. 1992. PMID: 1505967

10

Mouse mutations and human disorders are paired.

Hill R, Van Heyningen V. Hill R, et al. Among authors: van heyningen v. Trends Genet. 1992 Apr;8(4):119-20. doi: 10.1016/0168-9525(92)90359-C. Trends Genet. 1992. PMID: 1631953 Review. No abstract available.

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