L. Love-Gregory

发表

CD36 Modulates Fasting and Preabsorptive Hormone and Bile Acid Levels

N. Abumrad, N. Abumrad, Robyn A Tamboli, 2018, The Journal of clinical endocrinology and metabolism.

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.

Sebastian M. Armasu, Christine A. Williams, Audrey Y. Chu, 2019, American journal of human genetics.

An E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARγ Pro12Ala variant

M. Permutt, B. Suarez, J. Lin, 2002, Diabetologia.

Diagnostic Utility of Next-Generation Sequencing for Disorders of Somatic Mosaicism: A Five-Year Cumulative Cohort.

Jonathan W Heusel, Catherine E Cottrell, Samantha N McNulty, 2019, American journal of human genetics.

The fatty acid translocase gene CD36 and lingual lipase influence oral sensitivity to fat in obese subjects

S. Klein, N. Abumrad, M. Y. Pepino, 2012, Journal of Lipid Research.

CD36 genetics and the metabolic complications of obesity

N. Abumrad, L. Love-Gregory, 2011, Current opinion in clinical nutrition and metabolic care.

Beyond Panel-Based Testing: Exome Analysis Increases Sensitivity for Diagnosis of Genetic Kidney Disease.

Samantha N. McNulty, Parker C. Wilson, J. Gaut, 2020, Kidney360.

Prediction of striatal D2 receptor binding by DRD2/ANKK1 TaqIA allele status

D. Barch, K. Black, S. Eisenstein, 2016, Synapse.

Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation

J. Atkinson, S. Perkins, L. Love-Gregory, 2021, Frontiers in Medicine.

Variant in a common odorant-binding protein gene is associated with bitter sensitivity in people

M. Mitreva, M. H. Ozdener, Melania Melis, 2017, Behavioural Brain Research.

Cell-intrinsic lysosomal lipolysis is essential for macrophage alternative activation

Maxim N. Artyomov, D. O’Sullivan, B. Everts, 2014, Nature Immunology.

Physiological Mechanisms of Weight Gain-Induced Steatosis in People With Obesity.

S. Klein, E. Fabbrini, M. Yoshino, 2016, Gastroenterology.

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.

He Gao, Tim Kacprowski, Andres Metspalu, 2016, American journal of human genetics.

Forbidden knowledge

L. Love-Gregory, J. McCafferty, B. Schrag, 2003, Science and engineering ethics.

Variants in the CD36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol.

M. Permutt, D. Rao, S. Hunt, 2008, Human molecular genetics.

Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36 patient-oriented and epidemiological research

M. McCarthy, P. Deloukas, I. Borecki, 2016 .

A Multimodality Approach to Assessing Factor I Genetic Variants in Atypical Hemolytic Uremic Syndrome

Y. Sung, J. Atkinson, N. Pozzi, 2019, Kidney international reports.

Assessing the Pregnant Patient: A Review of New Potential Screening Tests

A. Gronowski, L. Love-Gregory, 2006 .

Adipose and Muscle Tissue Profile of CD36 Transcripts in Obese Subjects Highlights the Role of CD36 in Fatty Acid Homeostasis and Insulin Resistance

S. Klein, N. Abumrad, E. Fabbrini, 2014, Diabetes Care.

HNF4A genetic variants: role in diabetes

M. Permutt, L. Love-Gregory, 2007, Current opinion in clinical nutrition and metabolic care.

A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

Benjamin Glaser, M. Permutt, B. Suarez, 2004, Diabetes.

A Common CD36 Variant Influences Endothelial Function and Response to Treatment with Phosphodiesterase 5 Inhibition.

N. Abumrad, Leena Choi, L. Okamoto, 2016, The Journal of clinical endocrinology and metabolism.

CD36 maintains the gastric mucosa and associates with gastric disease

E. Gamazon, J. Mills, O. Kuda, 2021, Communications Biology.

Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population.

M. McCarthy, T. Frayling, B. Shields, 2004, Diabetes.

Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profile.

M. Connelly, S. Klein, J. Qi, 2011, Human molecular genetics.

Assessing allele frequencies of single nucleotide polymorphisms in DNA pools by pyrosequencing technology.

M. Permutt, J. Wasson, G. Skolnick, 2002, BioTechniques.

Evidence of common ancestry for the maple syrup urine disease (MSUD) Y438N allele in non-Mennonite MSUD patients.

R. Hillman, C. Phillips, L. Love-Gregory, 2002, Molecular genetics and metabolism.

Variants in Hepatocyte Nuclear Factor 4α Are Modestly Associated With Type 2 Diabetes in Pima Indians

Latisha Love-Gregory, Robert L Hanson, C. Bogardus, 2005 .

Searching for type 2 diabetes genes on chromosome 20.

M. Permutt, B. Suarez, B. Glaser, 2002, Diabetes.

Between a rock and a hard place: disclosing medical errors.

J. Ladenson, A. Gronowski, L. Love-Gregory, 2006, Clinical chemistry.

Identification of challenges and a framework for implementation of the AMP/ASCO/CAP classification guidelines for reporting somatic variants

Eric J. Duncavage, Bijal A. Parikh, Latisha Love-Gregory, 2020, Practical laboratory medicine.

Variants in the CD 36 gene associate with the metabolic syndrome and high-density lipoprotein cholesterol

M. Permutt, D. Rao, S. Hunt, 2008 .

Physiologic and genetic evidence links hemopexin to triglycerides in mice and humans

H. A. Lawson, S. Klein, C. Semenkovich, 2017, International Journal of Obesity.

Carrier detection and rapid newborn diagnostic test for the common Y393N maple syrup urine disease allele by PCR-RFLP: Culturally permissible testing in the Mennonite community

J. Dyer, R. Hillman, C. Phillips, 2001, Journal of Inherited Metabolic Disease.

Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36[S]

M. McCarthy, P. Deloukas, I. Borecki, 2016, Journal of Lipid Research.

Forbidden knowledge The challenge of immoralism

L. Love-Gregory, B. Schrag, K. Muskavitch, 2003 .

Identification of novel ALK rearrangements in gynecologic clear cell carcinoma

I. Hagemann, D. Cao, Lingxin Zhang, 2020, International journal of cancer.

Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36[S]

P. Deloukas, I. Borecki, A. Kraja, 2016, Journal of Lipid Research.