Tim Footz - Publications, H-index & Citations

Tim Footz

university of alberta

20H指数

64论文数

1.2K被引数

收录论文 22

发表时间

Fractalkine enhances oligodendrocyte regeneration and remyelination in a demyelination mouse model

STEM CELL REPORTS

IF5.1

2023-02-01

OAAI

de Almeida, Monique M. A.; Watson, Adrianne E. S.; Bibi, Sana; Dittmann, Nicole L.; Goodkey, Kara; Sharafodinzadeh, Pedram; Galleguillos, Danny; Nakhaei-Nejad, Maryam; Kosaraju, Jayasankar; Steinberg, Noam; Wang, Beatrix S.; Footz, Tim; Giuliani, Fabrizio; Wang, Jing; Sipione, Simonetta; Edgar, Julia M.; Voronova, Anastassia

Hepatoma Derived Growth Factor Enhances Oligodendrocyte Genesis from Subventricular Zone Precursor Cells

ASN NEURO

IF3.7

2022-03-16

OAAI

Li, Yutong; Dittmann, Nicole Leanne; Watson, Adrianne Eve Scovil; de Almeida, Monique Marylin Alves; Footz, Tim; Voronova, Anastassia

Fractalkine signaling regulates oligodendroglial cell genesis from SVZ precursor cells

STEM CELL REPORTS

IF5.1

2021-08-01

OAAI

Watson, Adrianne E. S.; de Almeida, Monique M. A.; Dittmann, Nicole L.; Li, Yutong; Torabi, Pouria; Footz, Tim; Vetere, Gisella; Galleguillos, Danny; Sipione, Simonetta; Cardona, Astrid E.; Voronova, Anastassia

Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins

MOLECULES

IF4.6

2021-06-09

OAAI

Chrystal, Paul W.; Footz, Tim; Hodges, Elizabeth D.; Jensen, Justin A.; Walter, Michael A.; Allison, W. Ted

Agathisflavone Modifies Microglial Activation State and Myelination in Organotypic Cerebellar Slices Culture

JOURNAL OF NEUROIMMUNE PHARMACOLOGY

IF3.5

2021-04-21

OAAI

de Almeida, Monique Marylin Alves; Pieropan, Francesca; Footz, Tim; David, Jorge Mauricio; David, Juceni Pereira; da Silva, Victor Diogenes Amaral; dos Santos Souza, Cleide; Voronova, Anastassia; Butt, Arthur Morgan; Costa, Silvia Lima

FOXQ1 is Differentially Expressed Across Breast Cancer Subtypes with Low Expression Associated with Poor Overall Survival

breast cancer

IF3.4

2021-03-01

OAAI

Elian, Fahed A.; Are, Ubah; Ghosh, Sunita; Nuin, Paulo; Footz, Tim; McMullen, Todd P. W.; Brindley, David N.; Walter, Michael A.

FOXQ1 is differentially expressed across breast cancer subtypes and potentially can serve as a prognostic marker

FASEB JOURNAL

IF4.2

2020-04-16

OAAI

Elian, Fahed; Are, Ubah; Nuin, Paulo; Footz, Tim; Brindley, David; McMullen, Todd; Walter, Michael

Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma

HUMAN MOLECULAR GENETICS

IF3.2

2018-12-17

OAAI

Lahola-Chomiak, Adrian A.; Footz, Tim; Nguyen-Phuoc, Kim; Neil, Gavin J.; Fan, Baojian; Allen, Ken F.; Greenfield, David S.; Parrish, Richard K.; Linkroum, Kevin; Pasquale, Louis R.; Leonhardt, Ralf M.; Ritch, Robert; Javadiyan, Shari; Craig, Jamie E.; Allison, W. T.; Lehmann, Ordan J.; Walter, Michael A.; Wiggs, Janey L.

FOXF2 is required for cochlear development in humans and mice

HUMAN MOLECULAR GENETICS

IF3.2

2018-12-17

OAAI

Bademci, Guney; Abad, Clemer; Incesulu, Armagan; Elian, Fahed; Reyahi, Azadeh; Diaz-Horta, Oscar; Cengiz, Filiz B.; Sineni, Claire J.; Seyhan, Serhat; Atli, Emine Ikbal; Basmak, Hikmet; Demir, Selma; Nik, Ali Moussavi; Footz, Tim; Guo, Shengru; Duman, Duygu; Fitoz, Suat; Gurkan, Hakan; Blanton, Susan H.; Walter, Michael A.; Carlsson, Peter; Walz, Katherina; Tekin, Mustafa

FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2018-05-22

OAAI

Doucette, Lance P.; Footz, Tim; Walter, Michael A.

Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma

HUMAN MOLECULAR GENETICS

IF3.2

2017-07-03

OAAI

Protas, Meredith E.; Weh, Eric; Footz, Tim; Kasberger, Jay; Baraban, Scott C.; Levin, Alex V.; Katz, L. Jay; Ritch, Robert; Walter, Michael A.; Semina, Elena V.; Gould, Douglas B.

Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger Syndrome

HUMAN MUTATION

IF3.7

2016-11-21

OAAI

Seifi, Morteza; Footz, Tim; Taylor, Sherry A. M.; Walter, Michael A.

Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome

ACTA OPHTHALMOLOGICA

IF2.8

2016-03-24

OAAI

Seifi, Morteza; Footz, Tim; Taylor, Sherry A. M.; Elhady, Ghada M.; Abdalla, Ebtesam M.; Walter, Michael A.

PITX2 Is Involved in Stress Response in Cultured Human Trabecular Meshwork Cells through Regulation of SLC13A3

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2011-09-28

OAAI

Strungaru, M. Hermina; Footz, Tim; Liu, Yi; Berry, Fred B.; Belleau, Pascal; Semina, Elena V.; Raymond, Vincent; Walter, Michael A.

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

HUMAN MOLECULAR GENETICS

IF3.2

2009-10-28

127

PREAI

Ye, Ming; Berry-Wynne, Karyn M.; Asai-Coakwell, Mika; Sundaresan, Periasamy; Footz, Tim; French, Curtis R.; Abitbol, Marc; Fleisch, Valerie C.; Corbett, Nathan; Allison, W. Ted; Drummond, Garry; Walter, Michael A.; Underhill, T. Michael; Waskiewicz, Andrew J.; Lehmann, Ordan J.

Severe Molecular Defects of a Novel FOXC1 W152G Mutation Result in Aniridia

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2009-08-01

PREAI

Ito, Yoko A.; Footz, Tim K.; Berry, Fred B.; Mirzayans, Farideh; Yu, May; Khan, Arif O.; Walter, Michael A.

Analysis of Mutations of the PITX2 Transcription Factor Found in Patients with Axenfeld-Rieger Syndrome

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2009-06-01

PREAI

Footz, Tim; Idrees, Faisal; Acharya, Moulinath; Kozlowski, Kathy; Walter, Michael A.