W. Paradee

发表

Characterization of Mice Ubiquitously Overexpressing Human 15-Lipoxygenase-1: Effect of Diabetes on Peripheral Neuropathy and Treatment with Menhaden Oil

E. Davidson, M. Yorek, L. Coppey, 2021, Journal of diabetes research.

TFH cells depend on Tcf1-intrinsic HDAC activity to suppress CTLA4 and guard B-cell help function

Jianmin Wang, Xiaoke Ma, Chengyu Liu, 2020, Proceedings of the National Academy of Sciences.

Molecular characterization of the 3p14.2 constitutive fragile site

C. Mullins, V. Jayasankar, W. Paradee, 1994 .

Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3.

T. Glover, D. Smith, B. Opalka, 1995, Genomics.

High‐throughput Screening of Mouse Knockout Lines Identifies True Lean and Obese Phenotypes

D. Powell, A. Sands, A. Suwanichkul, 2008, Obesity.

Neuropeptide S (NPS) neurons: Parabrachial identity and novel distributions

Joel C Geerling, Dake Huang, Silvia Gasparini, 2022, The Journal of comparative neurology.

Deletion of the Gene Encoding the Ubiquitously Expressed Glucose-6-phosphatase Catalytic Subunit-related Protein (UGRP)/Glucose-6-phosphatase Catalytic Subunit-β Results in Lowered Plasma Cholesterol and Elevated Glucagon*

J. K. Oeser, R. O’Brien, O. McGuinness, 2006, Journal of Biological Chemistry.

Cardiometabolic Consequences of Deleting the Regulator of G protein Signaling-2 (Rgs2) From Cells Expressing Agouti-Related Peptide or the ANG (Angiotensin) II Type 1A Receptor in Mice

C. Sigmund, G. Deng, K. Gibson-Corley, 2022, Hypertension.

A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.

R. Shridhar, T. Glover, D. Smith, 1996, Genomics.

The Cloning of Tumor Suppressor Genes from the Short Arm of Human Chromosome 3 that Play a Role in the Development of Renal Cell Carcinoma

David I. Smith, V. Shridhar, Wanguo Liu, 1995 .

Tcf1 and Lef1 are required for the immunosuppressive function of regulatory T cells

D. Meyerholz, Weiqun Peng, Zhouhao Zeng, 2019, The Journal of experimental medicine.

FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites.

T. Glover, D. Smith, B. Hall, 1996, Human molecular genetics.

Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function

S. T. Warren, S. Warren, H. Melikian, 1999, Neuroscience.

Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.

R. Shridhar, T. Glover, D. Smith, 1997, Genomics.

Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors.

F. Sarkar, R. Shridhar, T. Glover, 1996, Cancer research.

The FHIT gene is alternatively spliced in normal kidney and renal cell carcinoma

David I. Smith, L. Cannizzaro, W. Paradee, 1997, Oncogene.

D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13.

J. Horton, R. Taggart, C. Mullins, 1993, Human molecular genetics.

Tyr is Responsible for the Cctq1a QTL and Links Developmental Environment to Central Corneal Thickness Determination

Michael G. Anderson, T. Scheetz, A. Hedberg-Buenz, 2021, bioRxiv.

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

C. Gunter, D. Nelson, S. Warren, 1998, Human molecular genetics.

Frequent Breakpoints in the 3 pl 4 . 2 Fragile Site , FRA 3 B , in Pancreatic Tumors 1

David I. Smith, R. Shridhar, T. Glover, 2006 .

Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas

David I. Smith, D. Grignon, W. Sakr, 1997, Oncogene.