Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23

Genomics

Volumn 18, Issue 3, 1993, Pages 467-472

  Kimberling, William J ^a,d   Kumar, Shrawan ^a,d   Gabow, Patricia A ^b   Kenyon, Judith B ^a,d   Connolly, Christopher J ^a,d   Somlo, Stefan ^c  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^b UNIVERSITY OF COLORADO   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d CREIGHTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 4Q; DNA FLANKING REGION; GENE ISOLATION; GENE LOCATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; HUMAN CELL; KIDNEY POLYCYSTIC DISEASE; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

EID: 0027767585     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0888-7543(11)80001-7     Document Type: Article

References (42)

1. Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: Data for genetic counselling
2. Hypertension in autosomal dominant polycystic kidney disease
3. The molecular biology of acute lymphoblastic leukemia
4. Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene
5. A new interstitial deletion of chromosome No.4 de!(4) (q22::q25)
6. Specific endothelin binding sites in renal medullary collecting duct cells: Lack of interaction with ANP binding and cGMP signalling
7. Intracranial aneurysms in autosomal dominant polycystic kidney disease
8. Elevated c-myc protooncogene expression in autosomal recessive polycystic kidney disease
9. Cloning and chromosomal localization of a human endothelin ETA receptor
10. Segregation analysis of autosomal dominant polycystic kidney disease
11. Endothelin-1 promotes steroidogenesis and stimulates protooncogene expression in transformed murine Leydig cells
12. Deletion of the c-kit protooncogene in the human developmental defect piebald trait
13. Autosomal dominant polycystic kidney disease-More than a renal disease
14. Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease
15. Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16
16. The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region
17. Organization, structure, chromosomal assignment, and expression of the gene encoding the human endothelin-A receptor
18. Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1
19. Linkage heterogeneity of autosomal dominant polycystic kidney disease
20. Genetic linkage studies of autosomal dominant polycystic kidney disease: Search for the second gene in a large Sicilian family
21. Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1
22. Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
23. Chromosomal localization of the genes encoding the p50/p105 subunits of NF-kappa B (NFKB2) and the I kappa B/MAD-3 (NFKBI) inhibitor of NF-kappa B to 4q24 and 14q13, respectively
24. Related subunits of NF-kappa B map to two distinct loci associated with translocations in leukemia, NFKB1 and NFKB2
25. Genetic and physical maps of human chromosome 4 based on dinucleotide repeats
26. Report of the committee on the genetic constitution of chromosome 4
27. A comprehensive genetic linkage map of the human genome
28. Possible locus for polycystic kidney disease on chromosome 2
29. The diagnosis and prognosis of autosomal dominant polycystic kidney disease
30. Genetic heterogeneity of polycystic kidney disease in Europe
31. Possible genetic heterogeneity of Usher Syndrome type 2: A family unlinked to chromosome 1q markers
32. Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease
33. A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
34. Regional localization of the autosomal dominant polycystic kidney disease locus
35. A second genetic locus for autosomal dominant polycystic kidney disease
36. Interstitial deletion of 4(q21q25) in a liveborn male
37. Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markers
38. C-myc as an inducer of polycystic kidney disease in transgenic mice
39. A second-generation linkage map of the human genome
40. Abnormal extracellular matrix and excessive growth of human adult polycystic kidney disease epithelia
41. A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease families