RNA-Seq Reveals Activation of Both Common and Cytokine-Specific Pathways following Neutrophil Priming

por Wright, Helen L., Thomas, Huw B., Moots, Robert J., Edwards, Steven W.
Publicado 2013

Whose Gene Is It Anyway? The Effect of Preparation Purity on Neutrophil Transcriptome Studies

por Thomas, Huw B., Moots, Robert J., Edwards, Steven W., Wright, Helen L.
Publicado 2015

Differential changes in gene expression in human neutrophils following TNF‐α stimulation: Up‐regulation of anti‐apoptotic proteins and down‐regulation of proteins involved in death...

por Chiewchengchol, Direkrit, Wright, Helen L., Thomas, Huw B., Lam, Connie W., Roberts, Kate J., Hirankarn, Nattiya, Beresford, Michael W., Moots, Robert J., Edwards, Steven W.
Publicado 2015

Modelling the developmental spliceosomal craniofacial disorder Burn-McKeown syndrome using induced pluripotent stem cells

por Wood, Katherine A., Rowlands, Charlie F., Thomas, Huw B., Woods, Steven, O’Flaherty, Julieta, Douzgou, Sofia, Kimber, Susan J., Newman, William G., O’Keefe, Raymond T.
Publicado 2020

Early B-cell Factor 3–Related Genetic Disease Can Mimic Urofacial Syndrome

por Harkness, J. Robert, Beaman, Glenda M., Teik, Keng W., Sidhu, Sangeet, Sayer, John A., Cordell, Heather J., Thomas, Huw B., Wood, Katherine, Stuart, Helen M., Woolf, Adrian S., Newman, William G.
Publicado 2020

Disease modeling of core pre-mRNA splicing factor haploinsufficiency

por Wood, Katherine A, Rowlands, Charlie F, Qureshi, Wasay Mohiuddin Shaikh, Thomas, Huw B, Buczek, Weronika A, Briggs, Tracy A, Hubbard, Simon J, Hentges, Kathryn E, Newman, William G, O’Keefe, Raymond T
Publicado 2019

A homozygous missense variant in CHRM3 associated with familial urinary bladder disease

por Beaman, Glenda M., Galatà, Gabriella, Teik, Keng W., Urquhart, Jill E., Aishah, Ali, O'Sullivan, James, Bhaskar, Sanjeev S., Wood, Katherine A., Thomas, Huw B., O'Keefe, Raymond T., Woolf, Adrian S., Stuart, Helen M., Newman, William G.
Publicado 2019

Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54

por Smith, Thomas B., Rea, Alessandro, Thomas, Huw B., Thompson, Kyle, Oláhová, Monika, Maroofian, Reza, Zamani, Mina, He, Langping, Sadeghian, Saeid, Galehdari, Hamid, Lotan, Nava Shaul, Gilboa, Tal, Herman, Kristin C., McCorvie, Thomas J., Yue, Wyatt W., Houlden, Henry, Taylor, Robert W., Newman, William G., O’Keefe, Raymond T.
Publicado 2023

A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations

por Jayadev, Ranjay, Morais, Mychel R. P. T., Ellingford, Jamie M., Srinivasan, Sandhya, Naylor, Richard W., Lawless, Craig, Li, Anna S., Ingham, Jack F., Hastie, Eric, Chi, Qiuyi, Fresquet, Maryline, Koudis, Nikki-Maria, Thomas, Huw B., O’Keefe, Raymond T., Williams, Emily, Adamson, Antony, Stuart, Helen M., Banka, Siddharth, Smedley, Damian, Sherwood, David R., Lennon, Rachel
Publicado 2022

Comparison of in silico strategies to prioritize rare genomic variants impacting RNA splicing for the diagnosis of genomic disorders

por Rowlands, Charlie, Thomas, Huw B., Lord, Jenny, Wai, Htoo A., Arno, Gavin, Beaman, Glenda, Sergouniotis, Panagiotis, Gomes-Silva, Beatriz, Campbell, Christopher, Gossan, Nicole, Hardcastle, Claire, Webb, Kevin, O’Callaghan, Christopher, Hirst, Robert A., Ramsden, Simon, Jones, Elizabeth, Clayton-Smith, Jill, Webster, Andrew R., Douglas, Andrew G. L., O’Keefe, Raymond T., Newman, William G., Baralle, Diana, Black, Graeme C. M., Ellingford, Jamie M.
Publicado 2021