Kerem BS - Search Results

1

Correlation between genotype and phenotype in patients with cystic fibrosis.

Augarten A, Kerem BS, Kerem E, Gazit E, Yahav Y. Augarten A, et al. Among authors: kerem bs. N Engl J Med. 1994 Mar 24;330(12):866. N Engl J Med. 1994. PMID: 8114851 No abstract available.

2

Gene, RNA, and ASO-based therapeutic approaches in Cystic Fibrosis.

Allaire NE, Griesenbach U, Kerem B, Lueck JD, Stanleigh N, Oren YS. Allaire NE, et al. J Cyst Fibros. 2023 Mar;22 Suppl 1(Suppl 1):S39-S44. doi: 10.1016/j.jcf.2022.12.016. Epub 2023 Jan 17. J Cyst Fibros. 2023. PMID: 36658041 Free PMC article.

3

Cystic fibrosis manifested as undescended testis and absence of vas deferens.

Goshen R, Kerem E, Shoshani T, Kerem BS, Feigin E, Zamir O, Yahav Y. Goshen R, et al. Among authors: kerem bs, kerem e. Pediatrics. 1992 Dec;90(6):982-3. Pediatrics. 1992. PMID: 1359500 No abstract available.

4

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

Kerem E, Corey M, Kerem BS, Rommens J, Markiewicz D, Levison H, Tsui LC, Durie P. Kerem E, et al. Among authors: kerem bs. N Engl J Med. 1990 Nov 29;323(22):1517-22. doi: 10.1056/NEJM199011293232203. N Engl J Med. 1990. PMID: 2233932 Free article.

5

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.

Kerem BS, Zielenski J, Markiewicz D, Bozon D, Gazit E, Yahav J, Kennedy D, Riordan JR, Collins FS, Rommens JM, et al. Kerem BS, et al. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8447-51. doi: 10.1073/pnas.87.21.8447. Proc Natl Acad Sci U S A. 1990. PMID: 2236053 Free PMC article.

6

Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis.

Lemna WK, Feldman GL, Kerem B, Fernbach SD, Zevkovich EP, O'Brien WE, Riordan JR, Collins FS, Tsui LC, Beaudet AL. Lemna WK, et al. N Engl J Med. 1990 Feb 1;322(5):291-6. doi: 10.1056/NEJM199002013220503. N Engl J Med. 1990. PMID: 2296270 Free article.

7

Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus.

Kerem E, Corey M, Kerem B, Durie P, Tsui LC, Levison H. Kerem E, et al. J Pediatr. 1989 May;114(5):767-73. doi: 10.1016/s0022-3476(89)80134-9. J Pediatr. 1989. PMID: 2715890

8

Shoshani T, Kerem E, Szeinberg A, Augarten A, Yahav Y, Cohen D, Rivlin J, Tal A, Kerem B. Shoshani T, et al. J Clin Invest. 1994 Apr;93(4):1502-7. doi: 10.1172/JCI117128. J Clin Invest. 1994. PMID: 7512981 Free PMC article.

9

Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21.

Shoshani T, Augarten A, Yahav J, Gazit E, Kerem B. Shoshani T, et al. Hum Mol Genet. 1994 Apr;3(4):657-8. doi: 10.1093/hmg/3.4.657. Hum Mol Genet. 1994. PMID: 7520798 No abstract available.

10

A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews.

Shoshani T, Berkun Y, Yahav Y, Augarten A, Bashan N, Rivlin Y, Gazit E, Sereth H, Kerem E, Kerem BS. Shoshani T, et al. Among authors: kerem bs, kerem e. Genomics. 1993 Jan;15(1):236-7. doi: 10.1006/geno.1993.1046. Genomics. 1993. PMID: 7679367 No abstract available.

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