Works by McDermott, David H.

Results: 23

Risk of Superficial Fungal Infections in WHIM Syndrome.

Published in:

Dermatology & Therapy, 2025, v. 15, n. 5, p. 1173, doi. 10.1007/s13555-025-01396-0

By:

Strong, Jennifer;
Adhanom, Rutha;
Kim, Caleb S.;
Saito, Yoshine;
Meltzer, Jasmine C.;
Hallaert, Patrick;
Martinez, Sophia;
Salancy, Abigail;
Kong, Heidi H.;
Cowen, Edward W.;
Castelo-Soccio, Leslie;
Murphy, Philip M.;
McDermott, David H.;
Brownell, Isaac

Publication type:

Article

AMD3100 is a potent antagonist at CXCR4<sup>R334X</sup>, a hyperfunctional mutant chemokine receptor and cause of WHIM syndrome.

Published in:

Journal of Cellular & Molecular Medicine, 2011, v. 15, n. 10, p. 2071, doi. 10.1111/j.1582-4934.2010.01210.x

By:

McDermott, David H.;
Lopez, Joseph;
Deng, Francis;
Liu, Qian;
Ojode, Teresa;
Chen, Haoqian;
Ulrick, Jean;
Kwatemaa, Nana;
Kelly, Corin;
Anaya-O'Brien, Sandra;
Garofalo, Mary;
Marquesen, Martha;
Hilligoss, Dianne;
DeCastro, Rosamma;
Malech, Harry L.;
Murphy, Philip M.

Publication type:

Article

Chemokines and their receptors in infectious diesease.

Published in:

Springer Seminars in Immunopathology, 2000, v. 22, n. 4, p. 393, doi. 10.1007/s002810000052

By:

McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

Recalcitrant tinea capitis in WHIM syndrome.

Published in:

Skin Health & Disease, 2025, v. 5, n. 1, p. 41, doi. 10.1093/skinhd/vzae002

By:

Meltzer, Jasmine C;
Strong, Jennifer;
Martinez, Sophia;
Salancy, Abigail;
Adhanom, Rutha;
Cowen, Edward W;
Castelo-Soccio, Leslie;
Murphy, Philip M;
McDermott, David H;
Brownell, Isaac

Publication type:

Article

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1.

Published in:

Science Immunology, 2020, v. 5, n. 49, p. 1, doi. 10.1126/sciimmunol.abc9492

By:

Howson, Lauren J.;
Awad, Wael;
von Borstel, Anouk;
Lim, Hui Jing;
McWilliam, Hamish E. G.;
Sandoval-Romero, Maria L.;
Majumdar, Shamik;
Hamzeh, Abdul Rezzak;
Andrews, Thomas D.;
McDermott, David H.;
Murphy, Philip M.;
Le Nours, Jérôme;
Mak, Jeffrey Y. W.;
Liu, Ligong;
Fairlie, David P.;
McCluskey, James;
Villadangos, Jose A.;
Cook, Matthew C.;
Turner, Stephen J.;
Davey, Martin S.

Publication type:

Article

CXCR4 signaling determines the fate of hematopoietic multipotent progenitors by stimulating mTOR activity and mitochondrial metabolism.

Published in:

Science Signaling, 2024, v. 17, n. 860, p. 1, doi. 10.1126/scisignal.adl5100

By:

Rondeau, Vincent;
Kalogeraki, Maria;
Roland, Lilian;
Nader, Zeina Abou;
Gourhand, Vanessa;
Bonaud, Amélie;
Lemos, Julia;
Khamyath, Mélanie;
Moulin, Clémentine;
Schell, Bérénice;
Delord, Marc;
Bidaut, Ghislain;
Lecourt, Séverine;
Freitas, Christelle;
Anginot, Adrienne;
Mazure, Nathalie;
McDermott, David H.;
Parietti, Véronique;
Setterblad, Niclas;
Dulphy, Nicolas

Publication type:

Article

JAGN1 mutations in severe congenital neutropenia.

Published in:

British Journal of Haematology, 2021, v. 192, n. 1, p. 9, doi. 10.1111/bjh.17135

By:

McDermott, David H.;
Malech, Harry L.

Publication type:

Article

Genetic Variation in OAS1 Is a Risk Factor for Initial Infection with West Nile Virus in Man.

Published in:

PLoS Pathogens, 2009, v. 5, n. 2, p. 1, doi. 10.1371/journal.ppat.1000321

By:

K.^Lim, Jean;
Lisco, Andrea;
McDermott, David H.;
Huynh, Linda;
Ward, Jerrold M.;
Johnson, Bernard;
Johnson, Hope;
Pape, John;
A.^Foster, Gregory;
Krysztof, David;
Follmann, Dean;
L. Stramer, Susan;
Margolis, Leonid B.;
Murphy, Philip M.

Publication type:

Article

Multicenter Experience of Hematopoietic Stem Cell Transplantation in WHIM Syndrome.

Published in:

Journal of Clinical Immunology, 2022, v. 42, n. 1, p. 171, doi. 10.1007/s10875-021-01155-8

By:

Laberko, Alexandra;
Deordieva, Ekaterina;
Krivan, Gergely;
Goda, Vera;
Bhar, Saleh;
Kawahara, Yuta;
Rao, Kanchan;
Worth, Austen;
McDermott, David H.;
Balashov, Dmitry;
Maschan, Alexey;
Shcherbina, Anna

Publication type:

Article

Correction to: TREC Screening for WHIM Syndrome.

Published in:

2021

By:

Oman Evans II, Martin;
Petersen, Maureen M.;
Khojah, Amer;
Jyonouchi, Soma C.;
Edwardson, George S.;
Khan, Yasmin West;
Connelly, James Albert;
Morris, David;
Majumdar, Shamik;
McDermott, David H.;
Walter, Jolan E.;
Murphy, Philip M.

Publication type:

Correction Notice

TREC Screening for WHIM Syndrome.

Published in:

Journal of Clinical Immunology, 2021, v. 41, n. 3, p. 621, doi. 10.1007/s10875-020-00921-4

By:

Evans II, Martin Oman;
Petersen, Maureen M.;
Khojah, Amer;
Jyonouchi, Soma C.;
Edwardson, George S.;
Khan, Yasmin West;
Connelly, James Albert;
Morris, David;
Majumdar, Shamik;
McDermott, David H.;
Walter, Jolan E.;
Murphy, Philip M.

Publication type:

Article

Abnormal Newborn Screen in a WHIM Syndrome Infant.

Published in:

2019

By:

Evans II, Martin O.;
McDermott, David H.;
Murphy, Philip M.;
Petersen, Maureen M.

Publication type:

Letter

WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure.

Published in:

Journal of Clinical Immunology, 2019, v. 39, n. 6, p. 532, doi. 10.1007/s10875-019-00665-w

By:

Heusinkveld, Lauren E.;
Majumdar, Shamik;
Gao, Ji-Liang;
McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

Mechanisms of Sustained Neutrophilia in Patient WHIM-09, Cured of WHIM Syndrome by Chromothripsis.

Published in:

Journal of Clinical Immunology, 2018, v. 38, n. 1, p. 77, doi. 10.1007/s10875-017-0457-8

By:

Liu, Qian;
Li, Zhanzhuo;
Y. Yang, Alexander;
Gao, Ji-Liang;
S. Velez, Daniel;
J. Cho, Elena;
McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

WHIM syndrome: Immunopathogenesis, treatment and cure strategies.

Published in:

Immunological Reviews, 2019, v. 287, n. 1, p. 91, doi. 10.1111/imr.12719

By:

McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

Periodontal disease in patients with WHIM syndrome.

Published in:

Journal of Clinical Periodontology, 2024, v. 51, n. 4, p. 464, doi. 10.1111/jcpe.13940

By:

Brenchley, Laurie;
McDermott, David H.;
Gardner, Pamela J.;
Silva, Lakmali M.;
Gao, Ji‐Liang;
Cho, Elena;
Velez, Daniel;
Moutsopoulos, Niki M.;
Murphy, Philip M.;
Fraser, David

Publication type:

Article

Chromoanasynthesis as a cause of Jacobsen syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2020, v. 182, n. 11, p. 2533, doi. 10.1002/ajmg.a.61824

By:

Anzick, Sarah;
Thurm, Audrey;
Burkett, Sandra;
Velez, Daniel;
Cho, Elena;
Chlebowski, Colby;
Virtaneva, Kimmo;
Bruno, Daniel;
Martin, Clare B.;
Lang, David M.;
Brooks, Brian;
Martens, Craig;
McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

Assessment of cumulative evidence on genetic associations: interim guidelines.

Published in:

International Journal of Epidemiology, 2008, v. 37, n. 1, p. 120, doi. 10.1093/ije/dym159

By:

John PA Ioannidis;
Paolo Boffetta;
Julian Little;
Thomas R OÂBrien;
Andre G Uitterlinden;
Paolo Vineis;
David J Balding;
Anand Chokkalingam;
Siobhan M Dolan;
W Dana Flanders;
Julian PT Higgins;
Mark I McCarthy;
David H McDermott;
Grier P Page;
Timothy R Rebbeck;
Daniela Seminara;
Muin J Khoury

Publication type:

Article

CXCR4 antagonist AMD3100 redistributes leukocytes from primary immune organs to secondary immune organs, lung, and blood in mice.

Published in:

European Journal of Immunology, 2015, v. 45, n. 6, p. 1855, doi. 10.1002/eji.201445245

By:

Liu, Qian;
Li, Zhanzhuo;
Gao, Ji‐Liang;
Wan, Wuzhou;
Ganesan, Sundar;
McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

The effect of Rho kinase inhibition on long-term keratinocyte proliferation is rapid and conditional.

Published in:

Stem Cell Research & Therapy, 2014, v. 5, n. 2, p. 1, doi. 10.1186/scrt449

By:

Chapman, Sandra;
McDermott, David H.;
Kui Shen;
Moon Kyoo Jang;
McBride, Alison A.

Publication type:

Article

CCR5 Deficiency Is a Risk Factor for Early Clinical Manifestations of West Nile Virus Infection but not for Viral Transmission.

Published in:

Journal of Infectious Diseases, 2010, v. 201, n. 2, p. 178, doi. 10.1086/649426

By:

Lim, Jean K.;
McDermott, David H.;
Lisco, Andrea;
Foster, Gregory A.;
Krysztof, David;
Follmann, Dean;
Stramer, Susan L.;
Murphy, Philip M.

Publication type:

Article

Genetic Deficiency of Chemokine Receptor CCR5 Is a Strong Risk Factor for Symptomatic West Nile Virus Infection: A Meta-Analysis of 4 Cohorts in the US Epidemic.

Published in:

Journal of Infectious Diseases, 2008, v. 197, n. 2, p. 262, doi. 10.1086/524691

By:

Lim, Jean K.;
Louie, Christine Y.;
Glaser, Carol;
Jean, Cynthia;
Johnson, Bernard;
Johnson, Hope;
McDermott, David H.;
Murphy, Philip M.

Publication type:

Article

Cxcr4-haploinsufficient bone marrow transplantation corrects leukopenia in an unconditioned WHIM syndrome model.

Published in:

Journal of Clinical Investigation, 2018, v. 128, n. 8, p. 3312, doi. 10.1172/JCI120375

By:

Ji-Liang Gao;
Yim, Erin;
Siwicki, Marie;
Yang, Alexander;
Qian Liu;
Azani, Ari;
Owusu-Ansah, Albert;
McDermott, David H.;
Murphy, Philip M.

Publication type:

Article