Normal view MARC view ISBD view

Tannins from Syzygium guineense suppress Wnt signaling and proliferation of Wnt-dependent tumors through a direct effect on secreted Wnts. [electronic resource]

By:

Koval, Alexey

Contributor(s):

Producer: 20190924Description: 110-120 p. digitalISSN:

1872-7980

Subject(s):

Online resources:

Available from publisher's website

In: Cancer letters vol. 435

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

There are no comments on this title.

to post a comment.

Back to results

1001 Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis.
by Schrander-Stumpel, C T
1002 Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.
by Plomp, A S
1003 Psychosocial problems, coping strategies, and the need for information of parents of children with Prader-Willi syndrome and Angelman syndrome.
by van den Borne, H W
1004 A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32.
by Veugelers, M
1005 Genetic heterogeneity of gingival fibromatosis on chromosome 2p.
by Shashi, V
1006 Rett syndrome in adolescent and adult females: clinical and molecular genetic findings.
by Smeets, E
1007 Cryptic translocation t(5;18) in familial mental retardation.
by Vogels, A
1008 Metabolic studies in older mentally retarded patients: significance of metabolic testing and correlation with the clinical phenotype.
by Van Buggenhout, G J
1009 Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.
by Engelen, J J
1010 A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy.
by Steyaert, J
1011 Cloning, characterization, and chromosomal localization to 4p16 of the human gene (LRPAP1) coding for the alpha 2-macroglobulin receptor-associated protein and structural comparison with the murine gene coding for the 44-kDa heparin-binding protein.
by Van Leuven, F
1012 Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.
by Devriendt, K
1013 Clinical and molecular genetic features of congenital spinal muscular atrophy.
by Devriendt, K
1014 Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).
by Debeer, Ph
1015 Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita.
by Devriendt, K
1016 A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males.
by Meloni, I
1017 Oculocerebral syndrome with hypopigmentation (Cross syndrome). Report of two siblings born to consanguineous parents.
by Fryns, J P
1018 Genetic heterogeneity in Rieger eye malformation.
by Legius, E
1019 Longitudinal changes in cognitive and adaptive behavior in fragile X females: a prospective multicenter analysis.
by Fisch, G S
1020 Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome.
by Munroe, P B