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Results: 1 to 20 of 91

1.

An 8-bp deletion in mNOTCH4 intron 10 leads to its retention in mRNA and to synthesis of a truncated protein.

Auffray C, Gayon R, Benraiss A, Martin N, Laurendeau I, Garaud J, Lucas B, Boitard C, Krief P.

Exp Cell Res. 2006 Feb 1;312(3):233-44. Epub 2005 Nov 21.

PMID:
16300754
[PubMed - indexed for MEDLINE]
2.

Gene organization of human NOTCH4 and (CTG)n polymorphism in this human counterpart gene of mouse proto-oncogene Int3.

Sugaya K, Sasanuma S, Nohata J, Kimura T, Fukagawa T, Nakamura Y, Ando A, Inoko H, Ikemura T, Mita K.

Gene. 1997 Apr 21;189(2):235-44.

PMID:
9168133
[PubMed - indexed for MEDLINE]
3.

Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene.

Uyttendaele H, Marazzi G, Wu G, Yan Q, Sassoon D, Kitajewski J.

Development. 1996 Jul;122(7):2251-9.

PMID:
8681805
[PubMed - indexed for MEDLINE]
Free Article
4.

The mouse mammary tumor associated gene INT3 is a unique member of the NOTCH gene family (NOTCH4).

Gallahan D, Callahan R.

Oncogene. 1997 Apr 24;14(16):1883-90.

PMID:
9150355
[PubMed - indexed for MEDLINE]
Free Article
5.

Cloning, expression, and functional characterization of human cyclooxygenase-1 splicing variants: evidence for intron 1 retention.

Qin N, Zhang SP, Reitz TL, Mei JM, Flores CM.

J Pharmacol Exp Ther. 2005 Dec;315(3):1298-305. Epub 2005 Sep 1.

PMID:
16141368
[PubMed - indexed for MEDLINE]
Free Article
6.
7.

Glucocorticoid and growth factor synergism requirement for Notch4 chromatin domain activation.

Wu J, Bresnick EH.

Mol Cell Biol. 2007 Mar;27(6):2411-22. Epub 2007 Jan 12.

PMID:
17220278
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genetic analysis of the (CTG)n NOTCH4 polymorphism in 65 multiplex bipolar pedigrees.

Swift-Scanlan T, Lan TH, Fallin MD, Coughlin JM, Potash JB, DePaulo JR, McInnis MG.

Psychiatr Genet. 2002 Mar;12(1):43-7.

PMID:
11901359
[PubMed - indexed for MEDLINE]
9.

Methylation analysis of the NOTCH4 -25 C/T polymorphism in schizophrenia.

McDonald PP, O'reilly R, Singh SM.

Psychiatr Genet. 2011 Feb;21(1):5-13. doi: 10.1097/YPG.0b013e32834133bc.

PMID:
21085055
[PubMed - indexed for MEDLINE]
10.

Triplet repeat polymorphism in the NOTCH4 gene with the human major histocompatibility complex in a healthy population and patients with a salivary gland tumor in Japan.

Ando A, Sugaya K, Shigenari A, Naruse TK, Horiuchi M, Shiina T, Kawata H, Chen L, Ikemura T, Inoko H.

Tissue Antigens. 1997 Jul;50(1):66-70.

PMID:
9243759
[PubMed - indexed for MEDLINE]
11.

NUMB is a break of WNT-Notch signaling cycle.

Katoh M, Katoh M.

Int J Mol Med. 2006 Sep;18(3):517-21.

PMID:
16865239
[PubMed - indexed for MEDLINE]
12.

Aberrant Notch3 and Notch4 expression in human hepatocellular carcinoma.

Gramantieri L, Giovannini C, Lanzi A, Chieco P, Ravaioli M, Venturi A, Grazi GL, Bolondi L.

Liver Int. 2007 Sep;27(7):997-1007.

PMID:
17696940
[PubMed - indexed for MEDLINE]
13.

Impaired Notch4 activity elicits endothelial cell activation and apoptosis: implication for transplant arteriosclerosis.

Quillard T, Coupel S, Coulon F, Fitau J, Chatelais M, Cuturi MC, Chiffoleau E, Charreau B.

Arterioscler Thromb Vasc Biol. 2008 Dec;28(12):2258-65. doi: 10.1161/ATVBAHA.108.174995. Epub 2008 Sep 18.

PMID:
18802018
[PubMed - indexed for MEDLINE]
Free Article
14.

Receptor binding specificities of Herstatin and its intron 8-encoded domain.

Shamieh LS, Evans AJ, Denton MC, Clinton GM.

FEBS Lett. 2004 Jun 18;568(1-3):163-6.

PMID:
15196940
[PubMed - indexed for MEDLINE]
Free Article
15.

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population.

Parle-McDermott A, Pangilinan F, Mills JL, Kirke PN, Gibney ER, Troendle J, O'Leary VB, Molloy AM, Conley M, Scott JM, Brody LC.

Am J Med Genet A. 2007 Jun 1;143A(11):1174-80.

PMID:
17486595
[PubMed - indexed for MEDLINE]
16.

The role of the vascular endothelial growth factor-Delta-like 4 ligand/Notch4-ephrin B2 cascade in tumor vessel remodeling and endothelial cell functions.

Hainaud P, Contrerès JO, Villemain A, Liu LX, Plouët J, Tobelem G, Dupuy E.

Cancer Res. 2006 Sep 1;66(17):8501-10.

PMID:
16951162
[PubMed - indexed for MEDLINE]
Free Article
17.
18.
19.

crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1).

Conti V, Aghaie A, Cilli M, Martin N, Caridi G, Musante L, Candiano G, Castagna M, Fairen A, Ravazzolo R, Guenet JL, Puliti A.

Int J Mol Med. 2006 Oct;18(4):593-600.

PMID:
16964410
[PubMed - indexed for MEDLINE]
20.

Porcine Parkin: molecular cloning of PARK2 cDNA, expression analysis, and identification of a splicing variant.

Bjerre D, Madsen LB, Bendixen C, Larsen K.

Biochem Biophys Res Commun. 2006 Sep 1;347(3):803-13. Epub 2006 Jul 10.

PMID:
16844087
[PubMed - indexed for MEDLINE]

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