Pitx2 Regulates Procollagen Lysyl Hydroxylase (Plod) Gene Expression: Implications for the Pathology of Rieger Syndrome

por Hjalt, Tord A., Amendt, Brad A., Murray, Jeffrey C.
Publicado 2001

Hyperglycemia as a risk factor for the development of retinopathy of prematurity

por Mohamed, Shakir, Murray, Jeffrey C, Dagle, John M, Colaizy, Tarah
Publicado 2013

The effects of oral clefts on hospital use throughout the lifespan

por Wehby, George L, Pedersen, Dorthe Almind, Murray, Jeffrey C, Christensen, Kaare
Publicado 2012

Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study

por Pedersen, Dorthe Almind, Wehby, George L., Murray, Jeffrey C., Christensen, Kaare
Publicado 2016

A systematic review of limiting antigen avidity enzyme immunoassay for detection of recent HIV-1 infection to expand supported applications

por Kin-On Lau, Joseph, Murdock, Nicholas, Murray, Jeffrey, Justman, Jessica, Parkin, Neil, Miller, Veronica
Publicado 2022

Polymorphisms of CYP51A1 from Cholesterol Synthesis: Associations with Birth Weight and Maternal Lipid Levels and Impact on CYP51 Protein Structure

por Lewińska, Monika, Zelenko, Urska, Merzel, Franci, Golic Grdadolnik, Simona, Murray, Jeffrey C., Rozman, Damjana
Publicado 2013

Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression

por Clyman, Ronald I., Hills, Nancy K., Dagle, John M., Murray, Jeffrey C., Kelsey, Keegan
Publicado 2021

Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome

por Maciolek, Nicole L, Alward, Wallace LM, Murray, Jeffrey C, Semina, Elena V, McNally, Mark T
Publicado 2006

Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases

por Leslie, Elizabeth J., Standley, Jennifer, Compton, John, Bale, Sherri, Schutte, Brian C., Murray, Jeffrey C.
Publicado 2013

Genetic associations with neonatal thyroid stimulating hormone levels

por Alul, Farah Y., Shchelochkov, Oleg A., Berberich, Stanton L., Murray, Jeffrey C., Ryckman, Kelli K.
Publicado 2013

Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia

por Brémond-Gignac, Dominique, Bitoun, Pierre, Reis, Linda M., Copin, Henri, Murray, Jeffrey C., Semina, Elena V.
Publicado 2010

Transcriptome landscape of the human placenta

por Kim, Jinsil, Zhao, Keyan, Jiang, Peng, Lu, Zhi-xiang, Wang, Jinkai, Murray, Jeffrey C, Xing, Yi
Publicado 2012

Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations

por Yang, Tian, Jia, Zhonglin, Bryant-Pike, Whitney, Chandrasekhar, Anand, Murray, Jeffrey C, Fritzsch, Bernd, Bassuk, Alexander G
Publicado 2014

Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

por Mueller, Kathryn L., Murray, Jeffrey C., Michaelson, Jacob J., Christiansen, Morten H., Reilly, Sheena, Tomblin, J. Bruce
Publicado 2016

The US Food and Drug Administration's tentative approval process and the global fight against HIV

por Chahal, Harinder Singh, Murray, Jeffrey S, Shimer, Martin, Capella, Peter, Presto, Ryan, Valdez, Mary Lou, Lurie, Peter G
Publicado 2017

Impact of the US Food and Drug Administration registration of antiretroviral drugs on global access to HIV treatment

por Chahal, Harinder Singh, Capella, Peter, Presto, Ryan, Murray, Jeffrey S, Shimer, Martin, Valdez, Mary Lou, Lurie, Peter G
Publicado 2018

An Evaluation of US Food and Drug Administration’s Program to Register HIV Drugs for Use in Resource-Constrained Settings

por Chahal, Harinder Singh, Koukounas, Kalli, Capella, Peter, Presto, Ryan, Murray, Jeffrey S., Shimer, Martin, Riley, Karen, Valdez, Mary Lou
Publicado 2019

A novel nonsense mutation in keratin 10 causes a familial case of recessive epidermolytic ichthyosis

por Gutierrez, Jeydith A, Hannoush, Zeina C, Vargas, Luis G, Momany, Allison, Garcia, Carmen C, Murray, Jeffrey C, Dunnwald, Martine
Publicado 2013

Sustained virological response rates with direct-acting antivirals in black subjects with HCV genotype 1 infection: systematic analysis of clinical trials

por Struble, Kimberly, Chan-Tack, Kirk, Qi, Karen, Valappil, Thamban, Connelly, Sarah, Mishra, Poonam, Price, Dionne, Murray, Jeffrey, Birnkrant, Debra
Publicado 2019

Candidate gene and locus analysis of myopia

por Mutti, Donald O., Cooper, Margaret E., O'Brien, Sarah, Jones, Lisa A., Marazita, Mary L., Murray, Jeffrey C., Zadnik, Karla
Publicado 2007