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Oncogene|February 14, 2007
Caspase cleavage of the APC tumor suppressor and release of an amino-terminal domain is required for the transcription-independent function of APC in apoptosisJ Qian, K Steigerwald, K A Combs, et al.Journal of Autism and Developmental Disorders|July 14, 2001
The development of a stress survey schedule for persons with autism and other developmental disabilitiesJ Groden, A Diller, M Bausman, et al.Materials & Design|April 4, 2022
Additive manufacturing of Ti-Ni bimetallic structuresAli Afrouzian, Cory J Groden, David P Field, et al.Experimental Cell Research|May 1, 1983
Bloom's syndrome cells have an abnormal serum growth responseJ F Lechner, M E Kaighn, A M Jetten, et al.American Journal of Human Genetics|December 5, 1998
The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestryN A Ellis, S Ciocci, M Proytcheva, et al.Human Molecular Genetics|July 1, 1993
Identical APC exon 15 mutations result in a variable phenotype in familial adenomatous polyposisP Paul, T Letteboer, L Gelbert, et al.Research in Developmental Disabilities|January 1, 1987
Effects of fenfluramine on the behavior of autistic individualsG Groden, J Groden, M Dondey, et al.Genetic Testing|August 28, 1999
High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish originL Shahrabani-Gargir, R Shomrat, Y Yaron, et al.Human Mutation|March 3, 1998
A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome geneJ E Straughen, J Johnson, D McLaren, et al.Gastroenterology|August 7, 2001
Numerous colonic adenomas in an individual with Bloom's syndromeA M Lowy, J J Kordich, V Gismondi, et al.Pageof 6