P. Malloy

O. Hiort, Jining Wang, P. Malloy, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genetic disorders and defects in vitamin d action.

P. Malloy, D. Feldman, 2010, Endocrinology and metabolism clinics of North America.

Compound Heterozygous Mutations in the Vitamin D Receptor in a Patient With Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets With Alopecia

Jining Wang, P. Malloy, D. Feldman, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Inactivation of the human vitamin D receptor by caspase-3.

P. Malloy, D. Feldman, 2009, Endocrinology.

Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy.

M. Geffner, P. Malloy, D. Feldman, 2009, Bone.

A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia.

Jining Wang, P. Malloy, D. Feldman, 2007, Archives of biochemistry and biophysics.

Enhanced Coactivator Binding and Transcriptional Activation of Mutant Vitamin D Receptors From Patients With Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets by Phosphorylation and Vitamin D Analogs

Sungtae Kim, S. Christakos, Yan Liu, 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hereditary 1,25-dihydroxyvitamin D resistant rickets due to a mutation causing multiple defects in vitamin D receptor function.

S. Peleg, P. Malloy, D. Feldman, 2004, Endocrinology.

A Unique Insertion/Substitution in Helix H1 of the Vitamin D Receptor Ligand Binding Domain in a Patient With Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets

P. Malloy, D. Feldman, M. L. Reyes, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hereditary 1 , 25-Dihydroxyvitamin

S. Peleg, P. Malloy, D. Feldman, 2004 .

A novel mutation in helix 12 of the vitamin D receptor impairs coactivator interaction and causes hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia.

P. Malloy, D. Feldman, P. Clark, 2002, Molecular endocrinology.

Modulation of vitamin d receptor activity by the corepressor hairless: differential effects of hairless isoforms.

K. Jensen, Jining Wang, P. Malloy, 2009, Endocrinology.

Rapid isoelectric focusing in a vertical polyacrylamide minigel system.

E. F. Robertson, H. Reeves, P. Malloy, 1987, Analytical biochemistry.

The role of insulin‐like growth factor binding protein‐3 in the growth inhibitory actions of androgens in LNCaP human prostate cancer cells

Jining Wang, P. Malloy, D. Feldman, 2008, International journal of cancer.

IMPLEMENT A TION OF A COMPUTERIZED PROTOCOL FOR ANTICOAGULANT THERAPY

P. Malloy, 2012 .

An ochre mutation in the vitamin D receptor gene causes hereditary 1,25-dihydroxyvitamin D3-resistant rickets in three families.

B. O’Malley, Z. Hochberg, J. Pike, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Vitamin D receptor gene polymorphisms: analysis of ligand binding and hormone responsiveness in cultured skin fibroblasts.

P. Malloy, D. Feldman, C. Gross, 1998, Biochemical and biophysical research communications.

Hereditary Resistance to Vitamin D

P. Malloy, D. Feldman, 1999 .

The presence of a polymorphism at the translation initiation site of the vitamin D receptor gene is associated with low bone mineral density in postmenopausal mexican‐American women

R. Marcus, P. Malloy, M. Villa, 1996, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The Molecular Basis of Hereditary 1 , 25Dihydroxyvitamin 25Dihydroxyvitamin 25Dihydroxyvitamin D 3 Resistant Rickets in Seven Related Families

Z. Hochberg, J. Pike, P. Malloy, 2013 .

The molecular basis of hereditary 1,25-dihydroxyvitamin D3 resistant rickets in seven related families.

Z. Hochberg, J. Pike, P. Malloy, 1990, The Journal of clinical investigation.

Biological activity of 19‐nor, 10‐keto, 25‐hydroxyvitamin D3

G. Sivam, P. Malloy, D. Feldman, 1987, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The Vitamin D Receptor Gene Start Codon Polymorphism: A Functional Analysis of FokI Variants

P. Malloy, D. Feldman, A. Krishnan, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The role of the vitamin D receptor and ERp57 in photoprotection by 1α,25-dihydroxyvitamin D3.

Vanessa B. Sequeira, R. Mason, M. Rybchyn, 2012, Molecular endocrinology.

A novel mutation in the deoxyribonucleic acid-binding domain of the vitamin D receptor causes hereditary 1,25-dihydroxyvitamin D-resistant rickets.

P. Malloy, D. Feldman, A. Al-Ashwal, 1996, The Journal of clinical endocrinology and metabolism.

Hereditary 1 alpha,25-dihydroxyvitamin D-resistant rickets resulting from a mutation in the vitamin D receptor deoxyribonucleic acid-binding domain.

P. Malloy, D. Feldman, Y. Weisman, 1994, The Journal of clinical endocrinology and metabolism.

Candida albicans estrogen-binding protein gene encodes an oxidoreductase that is inhibited by estradiol.

P. Malloy, D. Feldman, A. Krishnan, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Cell-autonomous regulation of brown fat identity gene UCP1 by unliganded vitamin D receptor.

P. Malloy, B. Feldman, 2013, Molecular endocrinology.

Immunochemical localization of NADP-specific isocitrate dehydrogenase in Escherichia coli.

H. Reeves, P. Malloy, J. Swafford, 1983, Science.

Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor

E. Delvin, P. Malloy, D. Feldman, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Mutant vitamin D receptors which confer hereditary resistance to 1,25-dihydroxyvitamin D3 in humans are transcriptionally inactive in vitro.

B. O’Malley, J. Pike, P. Malloy, 1989, The Journal of biological chemistry.

Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor.

T. Srivastava, Jining Wang, P. Malloy, 2010, Molecular genetics and metabolism.

Darrell M. Wilson, Jining Wang, P. Malloy, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Vitamin D Deficiency, Rickets and Osteomalacia

P. Malloy, D. Feldman, 2003 .

Synthesis and Biological Evaluation of 1 r , 25-Dihydroxyvitamin D 3 Analogues Hydroxymethylated at C-26 †

M. A. Regueira, F. Sussman, P. Ordóñez-Morán, 2011 .

Point mutations in the human vitamin D receptor gene associated with hypocalcemic rickets.

B. O’Malley, R. Kesterson, D. Kieback, 1988, Science.

Oestrogen-binding protein in Candida albicans: antibody development and cellular localization by electron immunocytochemistry.

C. Ardies, P. Malloy, D. Feldman, 1995, Microbiology.

Glucocorticoids can promote androgen-independent growth of prostate cancer cells through a mutated androgen receptor

Donna M. Peehl, David Feldman, D. Peehl, 2000, Nature Medicine.

Cloning and expression of the gene from Candida albicans that encodes a high-affinity corticosteroid-binding protein.

P. Malloy, D. Feldman, X. Zhao, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Hereditary 1,25-dihydroxyvitamin D-resistant rickets in a Pomeranian dog caused by a novel mutation in the vitamin D receptor gene.

J. Gookin, P. Malloy, D. Feldman, 2009, Journal of veterinary internal medicine.

Hereditary 1,25-Dihydroxyvitamin D-resistant rickets.

P. Malloy, D. Feldman, 1997, Endocrine development.

CHAPTER 13 – Vitamin D: Biology, Action, and Clinical Implications

E. Balint, P. Malloy, D. Feldman, 2008 .

Human vitamin D receptor mutations: identification of molecular defects in hypocalcemic vitamin D resistant rickets.

B. O’Malley, D. Kieback, J. Pike, 1989, Advances in experimental medicine and biology.

Clinical evaluation of the Vitek Neisseria-Haemophilus Identification card

P. Schreckenberger, P. Malloy, W. Janda, 1987, Journal of clinical microbiology.

Genetic Disorders Of Vitamin D Synthesis and Action

W. Miller, P. Malloy, D. Feldman, 2018 .

Erratum: Glucocorticoids can promote androgen-independent growth of prostate cancer cells through a mutated androgen receptor (Nature Medicine (2000) 6 (703-706))

D. Peehl, N. Navone, P. Malloy, 2000 .

CHAPTER 72 – Hereditary 1,25-Dihydroxyvitamin D—Resistant Rickets

P. Malloy, 2005 .

The vitamin D receptor and the syndrome of hereditary 1,25-dihydroxyvitamin D-resistant rickets.

J. Pike, P. Malloy, D. Feldman, 1999, Endocrine reviews.

Hereditary 1,25-dihydroxyvitamin D resistant rickets: Molecular basis and implications for the role of 1,25(OH)2D3 in normal physiology

P. Malloy, D. Feldman, 1990, Molecular and Cellular Endocrinology.

Hereditary vitamin D resistant rickets caused by a novel mutation in the vitamin D receptor that results in decreased affinity for hormone and cellular hyporesponsiveness.

R. Bouillon, P. Malloy, D. Feldman, 1997, The Journal of clinical investigation.

Cloning and characterization of the gene encoding the ADP-ribosylation factor in Candida albicans.

P. Malloy, D. Feldman, K. Denich, 1992, Gene.

Novel pathways that contribute to the anti-proliferative and chemopreventive activities of calcitriol in prostate cancer

D. Peehl, L. Nonn, P. Malloy, 2007, The Journal of Steroid Biochemistry and Molecular Biology.

Identification of a functional vitamin D response element in the human insulin-like growth factor binding protein-3 promoter.

P. Malloy, D. Feldman, Lihong Peng, 2004, Molecular endocrinology.

A novel nonsense mutation in the ligand binding domain of the vitamin D receptor causes hereditary 1,25-dihydroxyvitamin D-resistant rickets.

R. Bouillon, P. Malloy, D. Feldman, 2002, Molecular genetics and metabolism.

Chapter 33 – Genetic Disorders of Vitamin D Synthesis and Action

W. Miller, P. Malloy, D. Feldman, 2013 .

Molecular Defects in the Vitamin D Receptor Associated with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets (HVDRR)

P. Malloy, D. Feldman, 2010 .

A novel inborn error in the ligand-binding domain of the vitamin D receptor causes hereditary vitamin D-resistant rickets.

W. Zhu, P. Malloy, D. Feldman, 2001, Molecular genetics and metabolism.

Vitamin DBiology, Action, and Clinical Implications

P. Malloy, D. Feldman, Coleman Gross, 2001 .

Vitamin D resistance.

P. Malloy, D. Feldman, David Feldman, 1999, The American journal of medicine.

Genetic defects of the 1,25-dihydroxyvitamin D3 receptor.

B. O’Malley, J. Pike, P. Malloy, 1991, Journal of receptor research.

Abnormal binding of vitamin D receptors to deoxyribonucleic acid in a kindred with vitamin D-dependent rickets, type II.

Z. Hochberg, J. Pike, P. Malloy, 1989, The Journal of clinical endocrinology and metabolism.

Interaction of the vitamin D receptor with a vitamin D response element in the Mullerian-inhibiting substance (MIS) promoter: regulation of MIS expression by calcitriol in prostate cancer cells.

Jining Wang, P. Malloy, D. Feldman, 2009, Endocrinology.

Comparison of four rapid methods for identification of Enterobacteriaceae from blood cultures

P. Schreckenberger, P. Malloy, M. Ducate, 1983, Journal of clinical microbiology.

Automated methods in microbiology: II. Identification and susceptibility testing.

P. Malloy, B. Miceika, M. Ducate, 1983, The American journal of medical technology.

PPARgamma agonists enhance human vascular endothelial adhesiveness by increasing ICAM-1 expression.

G. Reaven, P. Malloy, D. Feldman, 1999, Biochemical and biophysical research communications.

Growth inhibitory concentrations of androgens up-regulate insulin-like growth factor binding protein-3 expression via an androgen response element in LNCaP human prostate cancer cells.

Jining Wang, P. Malloy, D. Feldman, 2006, Endocrinology.

VITAMIN D RECEPTOR MUTATIONS AND HEREDITARY 1,25-DIHYDROXYVITAMIN D RESISTANT RICKETS

J. Pike, P. Malloy, D. Feldman, 1991 .

Inactivation of the human vitamin D receptor by caspase-3.

P. Malloy, D. Feldman, 2009, Endocrinology.

Cell-autonomous regulation of brown fat identity gene UCP1 by unliganded vitamin D receptor.

P. Malloy, B. Feldman, 2013, Molecular endocrinology.

Synthesis and biological evaluation of 1α,25-dihydroxyvitamin D(3) analogues hydroxymethylated at C-26.

M. A. Regueira, F. Sussman, P. Ordóñez-Morán, 2011, Journal of medicinal chemistry.