Roos D - Search Results

1

Location of the epitope for 7D5, a monoclonal antibody raised against human flavocytochrome b558, to the extracellular peptide portion of primate gp91phox.

Yamauchi A, Yu L, Pötgens AJ, Kuribayashi F, Nunoi H, Kanegasaki S, Roos D, Malech HL, Dinauer MC, Nakamura M. Yamauchi A, et al. Among authors: roos d. Microbiol Immunol. 2001;45(3):249-57. doi: 10.1111/j.1348-0421.2001.tb02614.x. Microbiol Immunol. 2001. PMID: 11345535 Free article.

2

Immunocytochemical discovery of the 22- to 23-Kd subunit of cytochrome b558 at the surface of human peripheral phagocytes.

Nakamura M, Sendo S, van Zwieten R, Koga T, Roos D, Kanegasaki S. Nakamura M, et al. Among authors: roos d. Blood. 1988 Nov;72(5):1550-2. Blood. 1988. PMID: 3179440 Free article.

3

PU.1 as an essential activator for the expression of gp91(phox) gene in human peripheral neutrophils, monocytes, and B lymphocytes.

Suzuki S, Kumatori A, Haagen IA, Fujii Y, Sadat MA, Jun HL, Tsuji Y, Roos D, Nakamura M. Suzuki S, et al. Among authors: roos d. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6085-90. doi: 10.1073/pnas.95.11.6085. Proc Natl Acad Sci U S A. 1998. PMID: 9600921 Free PMC article.

4

Detection of gp91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b558 biosynthesis.

Porter CD, Kuribayashi F, Parkar MH, Roos D, Kinnon C. Porter CD, et al. Among authors: roos d. Biochem J. 1996 Apr 15;315 ( Pt 2)(Pt 2):571-5. doi: 10.1042/bj3150571. Biochem J. 1996. PMID: 8615831 Free PMC article.

5

Hematologically important mutations: X-linked chronic granulomatous disease (third update).

Roos D, Kuhns DB, Maddalena A, Roesler J, Lopez JA, Ariga T, Avcin T, de Boer M, Bustamante J, Condino-Neto A, Di Matteo G, He J, Hill HR, Holland SM, Kannengiesser C, Köker MY, Kondratenko I, van Leeuwen K, Malech HL, Marodi L, Nunoi H, Stasia MJ, Ventura AM, Witwer CT, Wolach B, Gallin JI. Roos D, et al. Blood Cells Mol Dis. 2010 Oct 15;45(3):246-65. doi: 10.1016/j.bcmd.2010.07.012. Epub 2010 Aug 21. Blood Cells Mol Dis. 2010. PMID: 20729109 Free PMC article. Review.

6

Inherited p40phox deficiency differs from classic chronic granulomatous disease.

van de Geer A, Nieto-Patlán A, Kuhns DB, Tool AT, Arias AA, Bouaziz M, de Boer M, Franco JL, Gazendam RP, van Hamme JL, van Houdt M, van Leeuwen K, Verkuijlen PJ, van den Berg TK, Alzate JF, Arango-Franco CA, Batura V, Bernasconi AR, Boardman B, Booth C, Burns SO, Cabarcas F, Bensussan NC, Charbit-Henrion F, Corveleyn A, Deswarte C, Azcoiti ME, Foell D, Gallin JI, Garcés C, Guedes M, Hinze CH, Holland SM, Hughes SM, Ibañez P, Malech HL, Meyts I, Moncada-Velez M, Moriya K, Neves E, Oleastro M, Perez L, Rattina V, Oleaga-Quintas C, Warner N, Muise AM, López JS, Trindade E, Vasconcelos J, Vermeire S, Wittkowski H, Worth A, Abel L, Dinauer MC, Arkwright PD, Roos D, Casanova JL, Kuijpers TW, Bustamante J. van de Geer A, et al. Among authors: roos d. J Clin Invest. 2018 Aug 31;128(9):3957-3975. doi: 10.1172/JCI97116. Epub 2018 Aug 6. J Clin Invest. 2018. PMID: 29969437 Free PMC article.

7

A novel polymorphism in the coding region of CYBB, the human gp91-phox gene.

Kuribayashi F, de Boer M, Leusen JH, Verhoeven AJ, Roos D. Kuribayashi F, et al. Among authors: roos d. Hum Genet. 1996 May;97(5):611-3. doi: 10.1007/BF02281870. Hum Genet. 1996. PMID: 8655140

8

Functional epitope on human neutrophil flavocytochrome b558.

Burritt JB, Foubert TR, Baniulis D, Lord CI, Taylor RM, Mills JS, Baughan TD, Roos D, Parkos CA, Jesaitis AJ. Burritt JB, et al. Among authors: roos d. J Immunol. 2003 Jun 15;170(12):6082-9. doi: 10.4049/jimmunol.170.12.6082. J Immunol. 2003. PMID: 12794137

9

Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).

Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, de Boer M, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Garcia-Morato MB, Shephard JLV, Cagdas D, Tezcan I, Sherkat R, Mortaz E, Fayezi A, Shahrooei M, Wolach B, Blancas-Galicia L, Kanegane H, Kawai T, Condino-Neto A, Vihinen M, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Roos D, et al. Blood Cells Mol Dis. 2021 Dec;92:102596. doi: 10.1016/j.bcmd.2021.102596. Epub 2021 Jul 28. Blood Cells Mol Dis. 2021. PMID: 34547651

10

Splice site mutations are a common cause of X-linked chronic granulomatous disease.

de Boer M, Bolscher BG, Dinauer MC, Orkin SH, Smith CI, Ahlin A, Weening RS, Roos D. de Boer M, et al. Among authors: roos d. Blood. 1992 Sep 15;80(6):1553-8. Blood. 1992. PMID: 1520880 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

968 results

Search Page