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1

Digitale Medien

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17 (1995)

Friedman, Thomas B. ; Liang, Yong ; Weber, James L. ; [weitere]

[s.l.] : Nature Publishing Group

Nature genetics 9 (1995), S. 86-91

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ISSN: 1546-1718

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Medizin

Notizen: [Auszug] Two percent of the residents of Bengkala, Bali, have profound, congenital, neurosensory, nonsyndromal deafness due to an autosomal recessive mutation at the DFNB3 locus. We have employed a direct genorne–wide disequilibrium search strategy, allele–frequency–dependent homozygosity ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/ng0195-86

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2

Digitale Medien

Testis-derived Sertoli cells have a trophic effect on dopamine neurons and alleviate hemiparkinsonism in rats (1997)

Sanberg, Paul R. ; Borlongan, Cesario V. ; Othberg, Agneta I. ; [weitere]

[s.l.] : Nature Publishing Group

Nature medicine 3 (1997), S. 1129-1132

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ISSN: 1546-170X

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Medizin

Notizen: [Auszug] Neural tissue transplantation has become an alternative treatment for Parkinson's disease (PD)1,2 and other neurodegenerative disorders. The clinical use of neural grafts as a source of dopamine for Parkinson's disease patients, although beneficial, is associated with logistical and ethical issues. ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/nm1097-1129

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3

Digitale Medien

Linkage-disequilibrium mapping without genotyping (1998)

Cheung, Vivian G. ; Gregg, Jeffrey P. ; Gogolin-Ewens, Kathryn J. ; [weitere]

[s.l.] : Nature Publishing Group

Nature genetics 18 (1998), S. 225-230

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ISSN: 1546-1718

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Medizin

Notizen: [Auszug] Genomic mismatch scanning (GMS) is a technique that enriches for regions of identity by descent (IBD) between two individuals without the need for genotyping or sequencing. Regions of IBD selected by GMS are mapped by hybridization to a microarray containing ordered clones of genomic DNA from ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/ng0398-225

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4

Digitale Medien

A mutation in PDS causes non-syndromic recessive deafness (1998)

Li, Xiaoyan C. ; Everett, Lorraine A. ; Lalwani, Anil K. ; [weitere]

[s.l.] : Nature Publishing Group

Nature genetics 18 (1998), S. 215-217

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ISSN: 1546-1718

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Medizin

Notizen: [Auszug] A much as 10% of all hereditary deafness may be Pendred syndrome, an autosomal recessive disorder characterized by congenital sensorineural deafness and thyroid goitre (OMIM entry 274600; ref. 1). Variable intrafamilial expression has been noted, particularly with respect to goitre which may appear ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/ng0398-215

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5

Digitale Medien

Binding of α-foetoprotein to murine T cells (1975)

DATTWYLER, RAYMOND J. ; MURGITA, ROBERT A. ; TOMASI, THOMAS B.

[s.l.] : Nature Publishing Group

Nature 256 (1975), S. 656-657

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ISSN: 1476-4687

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik

Notizen: [Auszug] To define the cell type(s) affected by AFP we studied the binding of AFP to the surface of various cells involved in the immune reaction using direct immunofluorescence on preparations of thymus derived lymphochtes (T cells), bone marrow derived lymphocytes (B cells) and macrophages. Mouse ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/256656a0

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6

Digitale Medien

Hypermutation in T cells questioned (1995)

Kelsoe, Garnett ; Zheng, Biao ; Kepler, Thomas B.

[s.l.] : Nature Publishing Group

Nature 375 (1995), S. 286-286

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ISSN: 1476-4687

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik

Notizen: [Auszug] KELSOE ET AL. REPLY - Bachl and Wabl are mistaken in stating that we presented insufficient data for a proper analysis of our results. Mutations in Va genes arise in vivo as a consequence of reaction in the germinal centre (GC) or in vitro during the PCR. Both processes are ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/375286a0

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7

Digitale Medien

Molecular basis for interaction of the protein tyrosine kinase ZAP-70 with the T-cell receptor (1995)

Hatada, Marcos H. ; Lu, Xiaode ; Laird, Ellen R. ; [weitere]

[s.l.] : Nature Publishing Group

Nature 377 (1995), S. 32-38

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ISSN: 1476-4687

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik

Notizen: [Auszug] The crystal structure of the tandem SH2 domains of human ZAP-70 in complex with a peptide derived from the ζ-subunit of the T-cell receptor reveals an unanticipated interaction between the two domains. A coiled coil of α-helices connects the two SH2 domains, producing an interface that ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/377032a0

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8

Digitale Medien

Reduction of transcription by homologue asynapsis in Drosophila imaginal discs (1996)

Goldsborough, Andrew S. ; Kornberg, Thomas B.

[s.l.] : Nature Publishing Group

Nature 381 (1996), S. 807-810

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ISSN: 1476-4687

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik

Notizen: [Auszug] Ubx specifies haltere and abdominal identities in the Drosophila epidermis. Mutations that reduce its activity (for example null alleles such as Ubx1, deletions of the locus, and some regulatory mutations; see Fig. la) transform these cells to wing13. In contrast, mutations that increase its ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/381807a0

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9

Digitale Medien

Solution structure of human CTLA-4 and delineation of a CD80/CD86 binding site conserved in CD28 (1997)

Metzler, William J. ; Bajorath, Jürgen ; Fenderson, William ; [weitere]

[s.l.] : Nature Publishing Group

Nature structural biology 4 (1997), S. 527-531

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ISSN: 1072-8368

Quelle: Nature Archives 1869 - 2009

Thema: Biologie , Medizin

Notizen: [Auszug] The structure of human CTLA-4 reveals that residues Met 99, Tyr 100 and Tyr 104 of the M99 YPPPY104 motif are adjacent to a patch of charged surface residues on the A‘GFCC’ face of the protein. Mutation of these residues, which are conserved in the CTLA-4/CD28 family, significantly ...

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1038/nsb0797-527

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