Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Mf, Seldin"'
Publikováno v:
Blood. 83:3753-3757
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematologic disorder that affects both sexes equally. The biochemical defect in PNH resides in the incomplete enzymatic assembly of glycosylphosphatidylinositol (GPI) anchors used for su
Autor:
Rc, Briggs, Ja, Briggs, Ozer J, Sealy L, Ll, Dworkin, stephen kingsmore, Mf, Seldin, Gp, Kaur, Rs, Athwal, En, Dessypris
Publikováno v:
Europe PubMed Central
We have previously shown that the human myeloid cell nuclear differentiation antigen (MNDA) is expressed at both the antigen and mRNA levels specifically in human monocytes and granulocytes and earlier stage cells in the myeloid lineage. A 200 amino
Autor:
Da, Hosford, Fh, Lin, Wang Y, Stephen Caddick, Rees M, Nj, Parkinson, Barclay J, Rd, Cox, Rm, Gardiner, Denton P, Mf, Seldin, Chen B
Publikováno v:
Europe PubMed Central
To understand the cellular and molecular mechanisms that underlie generalized absence seizures sufficiently well to design rational, efficacious new therapies for patients, it is necessary to turn to animal models to gain insights into these mechanis
Publikováno v:
Europe PubMed Central
We report the molecular cloning of a cDNA encoding a high affinity human glycine transporter. An open reading frame of 1914 nucleotides encodes a 638-amino acid protein that transports glycine in a Na+/Cl(-)-dependent manner. In common with other Na+
Autor:
Yao Z; Immunex Cororation, 51 University Street, Seattle, Washington 98101, USA., Fanslow WC, Seldin MF, Rousseau AM, Painter SL, Comeau MR, Cohen JI, Spriggs MK
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2011 Nov 01; Vol. 187 (9), pp. 4392-402.
Autor:
Sr, Nash, Giros B, stephen kingsmore, Km, Kim, el-Mestikawy S, Dong Q, Fumagalli F, Mf, Seldin, Mg, Caron
Publikováno v:
Europe PubMed Central
Two genes were identified and characterized that express cDNAs related to previously identified neurotransmitter and/or osmolyte transporters, but which are expressed specifically in the kidney. RNA transcribed from one of these two genes (XT2) was f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::70ff5eda1cd9472b78485c5afcde14a9
http://europepmc.org/abstract/med/9932288
http://europepmc.org/abstract/med/9932288
Autor:
stephen kingsmore, Md, Barbosa, Vt, Tchernev, Jc, Detter, Ac, Lossie, Mf, Seldin, Rf, Holcombe
Publikováno v:
Europe PubMed Central
Chediak-Higashi syndrome (CHS) is a systemic disorder of human and mouse (beige, bg) that is characterized by aberrant intracellular protein kinesis and lysosomal trafficking. Affected individuals exhibit a severe primary immune deficiency that princ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d65d0246f9212b2a780b0bc85412034a
http://europepmc.org/abstract/med/8952226
http://europepmc.org/abstract/med/8952226
Autor:
Sr, Nash, Giros B, stephen kingsmore, Jm, Rochelle, St, Suter, Gregor P, Mf, Seldin, Mg, Caron
Publikováno v:
Europe PubMed Central
The complete coding sequence from a human creatine transporter cDNA was isolated from a kidney library. This transporter is a member of a superfamily of proteins which includes the family of Na(+)- and Cl(-)-dependent transporters responsible for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::86063d1087e144449bb8b3442b0c1a09
http://europepmc.org/abstract/med/7953292
http://europepmc.org/abstract/med/7953292
Autor:
Steven Pittler, Ak, Lee, Altherr MR, Ta, Howard, Mf, Seldin, Rl, Hurwitz, Jj, Wasmuth, Baehr W
Publikováno v:
Europe PubMed Central
We have determined the primary structures of the human and mouse retinal rod cGMP-gated cation channel by analysis of cDNA clones and amplified DNA. The open reading frames predicted polypeptides of 690 and 683 residues exhibiting 88% sequence simila
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9128ff2a74b2828739c3d154fdb4cecc
http://europepmc.org/abstract/med/1372902
http://europepmc.org/abstract/med/1372902
Autor:
Nolte, Jessica
Publikováno v:
Stem Cells & Development; 11/15/2021, Vol. 30 Issue 22, p1093-1102, 10p