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Items: 40

1.
2.

ABI sequencing analysis. Manipulation of sequence data from the ABI DNA sequencer.

Hagemann TL, Kwan SP.

Mol Biotechnol. 1999 Dec 1;13(2):137-52. Review.

PMID:
10934528
3.

Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemia.

Vihinen M, Kwan SP, Lester T, Ochs HD, Resnick I, Väliaho J, Conley ME, Smith CI.

Hum Mutat. 1999;13(4):280-5.

PMID:
10220140
4.
5.

Wiskott-Aldrich syndrome protein-deficient mice reveal a role for WASP in T but not B cell activation.

Snapper SB, Rosen FS, Mizoguchi E, Cohen P, Khan W, Liu CH, Hagemann TL, Kwan SP, Ferrini R, Davidson L, Bhan AK, Alt FW.

Immunity. 1998 Jul;9(1):81-91.

6.

BTKbase, mutation database for X-linked agammaglobulinemia (XLA).

Vihinen M, Brandau O, Brandén LJ, Kwan SP, Lappalainen I, Lester T, Noordzij JG, Ochs HD, Ollila J, Pienaar SM, Riikonen P, Saha BK, Smith CI.

Nucleic Acids Res. 1998 Jan 1;26(1):242-7.

7.

Variable expression of WASP in B cell lines of Wiskott-Aldrich syndrome patients.

Remold-O'Donnell E, Cooley J, Shcherbina A, Hagemann TL, Kwan SP, Kenney DM, Rosen FS.

J Immunol. 1997 May 1;158(9):4021-5.

PMID:
9126958
8.

SeqEd. Manipulation of sequence data and chromatograms from the ABI DNA sequencer analysis files.

Hagemann TL, Kwan SP.

Methods Mol Biol. 1997;70:55-63. No abstract available.

PMID:
9089602
9.

ABI analysis. Manipulation of sequence data from the ABI DNA sequencer.

Hagemann TL, Kwan SP.

Methods Mol Biol. 1997;70:39-54. No abstract available.

PMID:
9089601
10.

BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

Vihinen M, Belohradsky BH, Haire RN, Holinski-Feder E, Kwan SP, Lappalainen I, Lehväslaiho H, Lester T, Meindl A, Ochs HD, Ollila J, Vorechovsky I, Weiss M, Smith CI.

Nucleic Acids Res. 1997 Jan 1;25(1):166-71. Erratum in: Nucleic Acids Res 1997 May 1;25(9):1874.

11.

BTKbase: XLA-mutation registry.

Vihinen M, Brooimans RA, Kwan SP, Lehväslaiho H, Litman GW, Ochs HD, Resnick I, Schwaber JH, Vorĕchovsky I, Smith CI.

Immunol Today. 1996 Nov;17(11):502-6. No abstract available.

PMID:
8961625
12.

BTKbase, mutation database for X-linked agammaglobulinemia (XLA).

Vihinen M, Iwata T, Kinnon C, Kwan SP, Ochs HD, Vorechovský I, Smith CI.

Nucleic Acids Res. 1996 Jan 1;24(1):160-5.

14.
15.

BTKbase: a database of XLA-causing mutations. International Study Group.

Vihinen M, Cooper MD, de Saint Basile G, Fischer A, Good RA, Hendriks RW, Kinnon C, Kwan SP, Litman GW, Notarangelo LD, et al.

Immunol Today. 1995 Oct;16(10):460-5. Review. No abstract available.

PMID:
7576047
16.
17.
19.

Genomic organization of the Btk gene and exon scanning for mutations in patients with X-linked agammaglobulinemia.

Hagemann TL, Chen Y, Rosen FS, Kwan SP.

Hum Mol Genet. 1994 Oct;3(10):1743-9.

PMID:
7880320
20.

Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA).

Zhu Q, Zhang M, Rawlings DJ, Vihinen M, Hagemann T, Saffran DC, Kwan SP, Nilsson L, Smith CI, Witte ON, Chen SH, Ochs HD.

J Exp Med. 1994 Aug 1;180(2):461-70.

21.

A new RFLP marker, SP282, at the btk locus for genetic analysis in X-linked agammaglobulinaemia families.

Kwan SP, Walker AP, Hagemann T, Gupta S, Vayuvegula B, Ochs HD.

Prenat Diagn. 1994 Jun;14(6):493-6.

PMID:
7937587
22.

Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23.

Hagemann T, Surosky R, Monaco AP, Lehrach H, Rosen FS, Kwan SP.

Genomics. 1994 May 1;21(1):262-5.

PMID:
8088799
23.

A BstNI polymorphism at the BTK locus in Xq21.3-Xq22.

Hagemann T, Kwan SP.

Hum Mol Genet. 1993 Dec;2(12):2201. No abstract available.

PMID:
7906593
24.

A polymorphic dinucleotide repeat at the DXS7 locus.

Moore BJ, Kwan SP, Bech-Hansen NT.

Nucleic Acids Res. 1992 Feb 25;20(4):929. No abstract available.

25.

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3.

Kwan SP, Lehner T, Hagemann T, Lu B, Blaese M, Ochs H, Wedgwood R, Ott J, Craig IW, Rosen FS.

Genomics. 1991 May;10(1):29-33.

PMID:
1675197
26.

Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.

Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F.

Genomics. 1990 Feb;6(2):238-42.

PMID:
2307467
27.

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.

Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS.

Genomics. 1988 Jul;3(1):39-43.

PMID:
2906042
28.

Evidence for a defect in "switch" T cells in patients with immunodeficiency and hyperimmunoglobulinemia M.

Mayer L, Kwan SP, Thompson C, Ko HS, Chiorazzi N, Waldmann T, Rosen F.

N Engl J Med. 1986 Feb 13;314(7):409-13.

PMID:
3080678
29.

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

Kwan SP, Kunkel L, Bruns G, Wedgwood RJ, Latt S, Rosen FS.

J Clin Invest. 1986 Feb;77(2):649-52.

30.

Elastic scattering of polarized neutrons on 16O, 59Co, and Pb at 23 MeV.

Lam ST, Dawson WK, Elbakr SA, Fielding HW, Green PW, Helmer RL, van Heerden IJ, Hussein AH, Kwan SP, Neilson GC, Otsubo T, Sheppard DM, Sherif HS, Soukup J.

Phys Rev C Nucl Phys. 1985 Jul;32(1):76-82. No abstract available.

PMID:
9952804
31.

Isospin dependence in the central real part of the optical model potential.

Kwan SP, Lam ST, Neilson GC, Sherif HS.

Phys Rev C Nucl Phys. 1985 Jan;31(1):271-273. No abstract available.

PMID:
9952514
32.

Multiple immunoglobulin switch region homologies outside the heavy chain constant region locus.

Kirsch IR, Ravetch JV, Kwan SP, Max EE, Ney RL, Leder P.

Nature. 1981 Oct 15-21;293(5833):585-7. No abstract available.

PMID:
6793874
33.

Two kappa immunoglobulin genes are expressed in the myeloma S107.

Kwan SP, Max EE, Seidman JG, Leder P, Scharff MD.

Cell. 1981 Oct;26(1 Pt 1):57-66.

PMID:
6799208
34.

Nucleic acid and protein sequences of phosphocholine-binding light chains.

Kwan SP, Rudikoff S, Seidman JG, Leder P, Scharff MD.

J Exp Med. 1981 May 1;153(5):1366-70.

35.

Recombination events that activate, diversify, and delete immunoglobulin genes.

Leder P, Max EE, Seidman JG, Kwan SP, Scharff M, Nau M, Norman B.

Cold Spring Harb Symp Quant Biol. 1981;45 Pt 2:859-65.

PMID:
6790218
36.

Immunoglobulin V/J recombination is accompanied by deletion of joining site and variable region segments.

Seidman JG, Nau MM, Norman B, Kwan SP, Scharff M, Leder P.

Proc Natl Acad Sci U S A. 1980 Oct;77(10):6022-6.

37.

Fusion of mouse myeloma and spleen cells.

Yelton DE, Diamond BA, Kwan SP, Scharff MD.

Curr Top Microbiol Immunol. 1978;81:1-7. No abstract available.

PMID:
567551
38.

Purification of a putative precursor of globin messenger RNA from mouse nucleated erythroid cells.

Kwan SP, Wood TG, Lingrel JB.

Proc Natl Acad Sci U S A. 1977 Jan;74(1):178-82.

39.

[Environmental sanitation control in industry].

Kwan SP.

Taehan Kanho. 1975 Apr 25;14(2):55-9. Korean. No abstract available.

PMID:
1055850
40.

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