M. Luce

发表

Distribution of 13 truncating mutations in the neurofibromatosis 1 gene.

R. Heim, L. Kam-Morgan, C. Binnie, 1995, Human molecular genetics.

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC

H. Ostrer, K. Kinzler, B. Vogelstein, 1997, Nature Genetics.

Hepatoblastoma and APC gene mutation in familial adenomatous polyposis.

G. Petersen, S. Hamilton, M. Cayouette, 1996, Gut.

Human breast tumors containing non-DNA-binding immunoreactive (67 kDa) estrogen receptor

C. Benz, G. Scott, M. Luce, 2004, Breast Cancer Research and Treatment.

A multicenter proficiency trial of gene amplification (PCR) for the detection of HIV-1.

M. Ascher, H. Sheppard, M. Luce, 1991, Journal of acquired immune deficiency syndromes.

Attenuated familial adenomatous polyposis (AFAP) a phenotypically and genotypically distinctive variant of FAP

T. Smyrk, M. Cayouette, M. Luce, 1995, Cancer.

Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene

S. Powell, D. Ahnen, G. Petersen, 1998, Gut.

Phenotypic Expression of Disease in Families That Have Mutations in the 5 Region of the Adenomatous Polyposis Coli Gene

G. Petersen, S. Hamilton, M. Cayouette, 1997, Annals of Internal Medicine.

Reduction in heat shock gene expression correlates with increased thermosensitivity in senescent human fibroblasts.

M. Luce, V. Cristofalo, 1992, Experimental cell research.

The use and interpretation of commercial APC gene testing for familial adenomatous polyposis.

G. Petersen, S. Hamilton, M. Luce, 1997, The New England journal of medicine.

Screening for truncated NF1 proteins

R. Heim, L. Kam-Morgan, R. Farber, 1994, Nature Genetics.

APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis.

K. Kinzler, B. Vogelstein, S. Gruber, 1997, Gut.

This initial description of a spectrum of BRCA 1 mutations , two of which are recurrent in unrelated individuals from high-risk African American kindreds , should provide initial data for more-intensive genetic epidemiology studies in blacks of African descent

S. Neuhausen, M. Luce, S. Cummings, 2006 .

Rapid identification of RT-PCR clones containing translation-terminating mutations.

C. Boland, L. Kam-Morgan, C. Binnie, 1997, Mutation research.

In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer.

Sajeev P. Cherian, M. Hawn, L. Kam-Morgan, 1995, Gastroenterology.

Decreased accuracy of protein synthesis in extracts from aging human diploid fibroblasts

M. Luce, C. Bunn, 1989, Experimental Gerontology.

Altered sensitivity of protein synthesis to paromomycin in extracts from aging human diploid fibroblasts

M. Luce, C. Bunn, 1987, Experimental Gerontology.

The accuracy of protein synthesis in reticulocyte and HeLa cell lysates.

M. Luce, C. Bunn, K. Tschanz, 1985, Biochimica et biophysica acta.

Metallothionein expression and stress responses in aging human diploid fibroblasts

M. Luce, C. Bunn, Jeffrey P. Schyberg, 1993, Experimental Gerontology.

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

G. Petersen, M. Luce, F. Giardiello, 2001, Familial Cancer.

Genetic alterations and epithelial dysplasia in juvenile polyposis syndrome and sporadic juvenile polyps.

C. Moskaluk, A. Rashid, B. Rezai, 1997, The American journal of pathology.

Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N'-nitro-N-nitrosoguanidine.

M. Hawn, C. Boland, M. Luce, 1996, The Journal of clinical investigation.

Pathology and genetic testing

R. A. Decker, S. Markowitz, A. Thor, 1997 .

Human papillomavirus detection and p53 expression in clear‐cell adenocarcinoma of the vagina and cervix

S. Waggoner, M. Luce, A. Herbst, 1994, Obstetrics and gynecology.

Mutational analysis of patients with neurofibromatosis, type 1 (NF1) and malignant myeloid disorders using a protein truncation assay.

M. Cayouette, M. Luce, K. Shannon, 1995 .

Identification of DNA mismatch repair gene mutations in hereditary nonpolyposis colon cancer patients

L. Kam-Morgan, C. Binnie, M. Cayouette, 1996, International journal of cancer.

HLA-DQ alpha allele and genotype frequencies in various human populations, determined by using enzymatic amplification and oligonucleotide probes.

M. Stoneking, W. Klitz, M. Luce, 1990, American journal of human genetics.

p53 protein expression and gene analysis in clear cell adenocarcinoma of the vagina and cervix.

J. Boyd, H. Takahashi, S. Waggoner, 1996, Gynecologic oncology.

Ovarian neoplasm and endometrioid carcinoma in a patient with Turcot syndrome.

M. Luce, M. Bialer, F. Giardiello, 1997, Journal of pediatric gastroenterology and nutrition.

Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders.

M. Cayouette, M. Luce, K. Shannon, 1997, The New England journal of medicine.

Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes.

O. Kallioniemi, B. Ward, H. Nevanlinna, 1997, Human molecular genetics.

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

K Offit, A Oliphant, S. Loader, 1997, JAMA.

UvA-DARE ( Digital Academic Repository ) APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis

B. Vogelstein, S. Gruber, S. Piantadosi, 1998 .