Krantz ID - Search Results

1

KILLER/DR5 is a DNA damage-inducible p53-regulated death receptor gene.

Wu GS, Burns TF, McDonald ER 3rd, Jiang W, Meng R, Krantz ID, Kao G, Gan DD, Zhou JY, Muschel R, Hamilton SR, Spinner NB, Markowitz S, Wu G, el-Deiry WS. Wu GS, et al. Among authors: krantz id. Nat Genet. 1997 Oct;17(2):141-3. doi: 10.1038/ng1097-141. Nat Genet. 1997. PMID: 9326928 No abstract available.

2

Expanded non-invasive prenatal diagnostics.

Spinner NB, Krantz ID. Spinner NB, et al. Among authors: krantz id. Nat Med. 2019 Mar;25(3):361-362. doi: 10.1038/s41591-019-0386-6. Nat Med. 2019. PMID: 30804517 No abstract available.

3

Alagille syndrome.

Krantz ID, Piccoli DA, Spinner NB. Krantz ID, et al. J Med Genet. 1997 Feb;34(2):152-7. doi: 10.1136/jmg.34.2.152. J Med Genet. 1997. PMID: 9039994 Free PMC article. Review.

4

Mutations in the human Jagged1 gene are responsible for Alagille syndrome.

Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoli DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC. Oda T, et al. Among authors: krantz id. Nat Genet. 1997 Jul;16(3):235-42. doi: 10.1038/ng0797-235. Nat Genet. 1997. PMID: 9207787

5

Novel microdeletion syndromes.

Krantz ID, Spinner NB. Krantz ID, et al. Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):323-6. doi: 10.1002/ajmg.c.30150. Am J Med Genet C Semin Med Genet. 2007. PMID: 17910074 Review. No abstract available.

6

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.

Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB. Li L, et al. Among authors: krantz id. Nat Genet. 1997 Jul;16(3):243-51. doi: 10.1038/ng0797-243. Nat Genet. 1997. PMID: 9207788

7

Consequences of JAG1 mutations.

Kamath BM, Bason L, Piccoli DA, Krantz ID, Spinner NB. Kamath BM, et al. Among authors: krantz id. J Med Genet. 2003 Dec;40(12):891-5. doi: 10.1136/jmg.40.12.891. J Med Genet. 2003. PMID: 14684686 Free PMC article.

8

Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization.

Krantz ID, Rand EB, Genin A, Hunt P, Jones M, Louis AA, Graham JM Jr, Bhatt S, Piccoli DA, Spinner NB. Krantz ID, et al. Am J Med Genet. 1997 May 2;70(1):80-6. Am J Med Genet. 1997. PMID: 9129746

9

Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families.

Krantz ID, Colliton RP, Genin A, Rand EB, Li L, Piccoli DA, Spinner NB. Krantz ID, et al. Am J Hum Genet. 1998 Jun;62(6):1361-9. doi: 10.1086/301875. Am J Hum Genet. 1998. PMID: 9585603 Free PMC article.

10

Craniosynostosis in Alagille syndrome.

Kamath BM, Stolle C, Bason L, Colliton RP, Piccoli DA, Spinner NB, Krantz ID. Kamath BM, et al. Among authors: krantz id. Am J Med Genet. 2002 Oct 1;112(2):176-80. doi: 10.1002/ajmg.10608. Am J Med Genet. 2002. PMID: 12244552

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