MAS promoter regulation: a role for Sry and tyrosine nitration of the KRAB domain of ZNF274 as a feedback mechanism.

Jeremy W. Prokop , Frank J. Rauscher , Hongzhuang Peng , Yuanjie Liu
Clinical Science 126 ( 10) 727 -738

6
2014
Beyond thermoregulation: metabolic function of cetacean blubber in migrating bowhead and beluga whales

H. C. Ball , R. L. Londraville , J. W. Prokop , John C. George
Journal of Comparative Physiology B-biochemical Systemic and Environmental Physiology 187 ( 1) 235 -252

17
2017
Chromosome Y genetic variants: impact in animal models and on human disease

J. W. Prokop , C. F. Deschepper
Physiological Genomics 47 ( 11) 525 -537

22
2015
Sept8/SEPTIN8 involvement in cellular structure and kidney damage is identified by genetic mapping and a novel human tubule hypoxic model.

Jeremy W. Prokop , Leah C. Solberg Woods , Michael R. Garrett , Patrick B. Kyle
Scientific Reports 11 ( 1) 2071 -2071

2021
Kinetic Characterization of ASXL1/2-Mediated Allosteric Regulation of the BAP1 Deubiquitinase.

Surbhi Joshi , Jacob P. Mandell , Paul R. Collop , Kasirajan Ayyanathan
Molecular Cancer Research

2021
Emerging Role of ODC1 in Neurodevelopmental Disorders and Brain Development.

Caleb P. Bupp , Jeremy W. Prokop , Daniel B. Campbell , Daniel Vogt
Genes 12 ( 4) 470

2021
Perinatal Manifestations of DARS2-Associated Leukoencephalopathy With Brainstem and Spinal Cord Involvement and Lactate Elevation (LBSL)

Laurie H. Seaver , Laurie H. Seaver , Jeremy W. Prokop , Jason Umfleet
Child Neurology Open 8

2
2021
Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.

Jeremy W. Prokop , Nan Cher Yeo , Christian Ottmann , Surya B. Chhetri
Journal of The American Society of Nephrology 29 ( 5) 1525 -1535

16
2018
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay.

Susan M Hiatt , Matthew B Neu , Ryne C Ramaker , Andrew A Hardigan
PLOS Genetics 14 ( 11) 1 -16

12
2018
RNF213 variants in a child with PHACE syndrome and moyamoya vasculopathy.

Kala F. Schilter , Jack E. Steiner , Wendy Demos , Mohit Maheshwari
American Journal of Medical Genetics Part A 173 ( 9) 2557 -2561

8
2017
A method for in silico identification of SNAIL/SLUG DNA binding potentials to the E-box sequence using molecular dynamics and evolutionary conserved amino acids

Jeremy W. Prokop , Yuanjie Liu , Amy Milsted , Hongzhuang Peng
Journal of Molecular Modeling 19 ( 9) 3463 -3469

15
2013
49
2014
Structural libraries of protein models for multiple species to understand evolution of the renin-angiotensin system.

Jeremy W. Prokop , Victoria Petri , Mary E. Shimoyama , Ingrid K.M. Watanabe
General and Comparative Endocrinology 215 106 -116

9
2015
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder

Susan M. Hiatt , Michelle L. Thompson , Jeremy W. Prokop , James M.J. Lawlor
American Journal of Human Genetics 104 ( 4) 701 -708

4
2019
7
2019
Expanding the phenotype of the CDKL5 deficiency disorder: Are seizures mandatory?

Conor I. MacKay , David Bick , Jeremy W. Prokop , Ivan Muñoz
American Journal of Medical Genetics Part A 182 ( 5) 1217 -1222

3
2020
Functional domain analysis of SOX18 transcription factor using a single-chain variable fragment-based approach.

Johannes Zuegg , Stephen Mahler , Mathias Francois , Frank R. Fontaine
mAbs 10 ( 4) 596 -606

4
2018
Mutations in RABL3 alter KRAS prenylation and are associated with hereditary pancreatic cancer.

Jill A. Rosenfeld , Andrew G. Cox , John Hedgepeth , Julia I. Wucherpfennig
Nature Genetics 51 ( 9) 1308 -1314

20
2019
Molecular modeling in the age of clinical genomics, the enterprise of the next generation.

Jeremy W. Prokop , Jozef Lazar , Gabrielle Crapitto , D. Casey Smith
Journal of Molecular Modeling 23 ( 3) 75 -75

29
2017
Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats.

Gregory R. Keele , Jeremy W. Prokop , Hong He , Katie Holl
Obesity 26 ( 1) 213 -222

33
2018