Works matching IS 09646906 AND DT 1998 AND VI 7 AND IP 10

Results: 32

The genetics of psoriasis: a complex disorder of the skin and immune system.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1537, doi. 10.1093/hmg/7.10.1537

By:

Bhalerao, Jayant;
Bowcock, Anne M.

Publication type:

Article

Ribozymes as therapeutic tools for genetic disease.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1649, doi. 10.1093/hmg/7.10.1649

By:

Phylactou, Leonidas A.;
Kilpatrick, Michael W.;
Wood, Matthew J.A.

Publication type:

Article

Mouse mutagenesis--systematic studies of mammalian gene function.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1627, doi. 10.1093/hmg/7.10.1627

By:

Brown, Steve D. M.;
Nolan, Patrick M.

Publication type:

Article

Engineering mammalian chromosomes.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1635, doi. 10.1093/hmg/7.10.1635

By:

Grimes, Brenda;
Cooke, Howard

Publication type:

Article

Position effect in human genetic disease.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1611, doi. 10.1093/hmg/7.10.1611

By:

Kleinjan, Dirk‐Jan;
van Heyningen, Veronica

Publication type:

Article

The role of the SMN gene in proximal spinal muscular atrophy.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1531, doi. 10.1093/hmg/7.10.1531

By:

Lefebvre, Suzie;
Bürglen, Lydie;
Frézal, Jean;
Munnich, Arnold;
Melki, Judith

Publication type:

Article

Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the art.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1573, doi. 10.1093/hmg/7.10.1573

By:

Smeitink, J. A. M.;
Loeffen, J. L. C. M.;
Triepels, R. H.;
Smeets, R. J. P.;
Trijbels, J. M. F.;
van den Heuvel, L. P.

Publication type:

Article

Gene defect behind APECED: a new clue to autoimmunity.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1547, doi. 10.1093/hmg/7.10.1547

By:

Björses, Petra;
Aaltonen, Johanna;
Horelli‐Kuitunen, Nina;
Yaspo, Marie‐Laure;
Peltonen, Leena

Publication type:

Article

A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1599, doi. 10.1093/hmg/7.10.1599

By:

Morison, Ian M.;
Reeve, Anthony E.

Publication type:

Article

The hereditary periodic fever syndromes: molecular analysis of a new family of inflammatory diseases.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1581, doi. 10.1093/hmg/7.10.1581

By:

Centola, Michael;
Aksentijevich, Ivona;
Kastner, Daniel L.

Publication type:

Article

The therapeutic reactivation of fetal haemoglobin.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1655, doi. 10.1093/hmg/7.10.1655

By:

Olivieri, Nancy F.;
Weatherall, D. J.

Publication type:

Article

ATM: from gene to function.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1555, doi. 10.1093/hmg/7.10.1555

By:

Rotman, Galit;
Shiloh, Yosef

Publication type:

Article

A practical guide to orient yourself in the labyrinth of genome databases.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1641, doi. 10.1093/hmg/7.10.1641

By:

Borsani, Giuseppe;
Ballabio, Andrea;
Banfi, Sandro

Publication type:

Article

Chromosome painting: a useful art.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1619, doi. 10.1093/hmg/7.10.1619

By:

Ried, Thomas;
Schröck, Evelin;
Ning, Yi;
Wienberg, Johannes

Publication type:

Article

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1589, doi. 10.1093/hmg/7.10.1589

By:

Kalatzis, Vasiliki;
Petit, Christine

Publication type:

Article

Two rights make a wrong: human left-right malformations.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1565, doi. 10.1093/hmg/7.10.1565

By:

Casey, Brett

Publication type:

Article

The therapeutic reactivation of fetal haemoglobin.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1655, doi. 10.1093/hmg/7.10.1655

By:

Olivieri, Nancy F.;
Weatherall, D. J.

Publication type:

Article

Ribozymes as therapeutic tools for genetic disease.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1649, doi. 10.1093/hmg/7.10.1649

By:

Phylactou, Leonidas A.;
Kilpatrick, Michael W.;
Wood, Matthew J. A.

Publication type:

Article

A practical guide to orient yourself in the labyrinth of genome databases.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1641, doi. 10.1093/hmg/7.10.1641

By:

Borsani, Giuseppe;
Ballabio, Andrea;
Banfi, Sandro

Publication type:

Article

Engineering mammalian chromosomes.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1635, doi. 10.1093/hmg/7.10.1635

By:

Grimes, Brenda;
Cooke, Howard

Publication type:

Article

The hereditary periodic fever syndromes: molecular analysis of a new family of inflammatory diseases.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1581, doi. 10.1093/hmg/7.10.1581

By:

Centola, Michael;
Aksentijevich, Ivona;
Kastner, Daniel L.

Publication type:

Article

Chromosome painting: a useful art.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1619, doi. 10.1093/hmg/7.10.1619

By:

Ried, Thomas;
Schröck, Evelin;
Ning, Yi;
Wienberg, Johannes

Publication type:

Article

Position effect in human genetic disease.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1611, doi. 10.1093/hmg/7.10.1611

By:

Kleinjan, Dirk-Jan;
Van Heyningen, Veronica

Publication type:

Article

A catalogue of imprinted genes and parent‐of‐origin effects in humans and animals.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1599, doi. 10.1093/hmg/7.10.1599

By:

Morison, Ian M.;
Reeve, Anthony E.

Publication type:

Article

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1589, doi. 10.1093/hmg/7.10.1589

By:

Kalatzis, Vasiliki;
Petit, Christine

Publication type:

Article

Mouse mutagenesis—systematic studies of mammalian gene function.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1627, doi. 10.1093/hmg/7.10.1627

By:

Brown, Steve D. M.;
Nolan, Patrick M.

Publication type:

Article

Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the art.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1573, doi. 10.1093/hmg/7.10.1573

By:

Smeitink, J. A. M.;
Loeffen, J. L. C. M.;
Triepels, R. H.;
Smeets, R. J. P.;
Trijbels, J. M. F.;
van den Heuvel, L. P.

Publication type:

Article

Two rights make a wrong: human left–right malformations.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1565, doi. 10.1093/hmg/7.10.1565

By:

Casey, Brett

Publication type:

Article

ATM: from gene to function.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1555, doi. 10.1093/hmg/7.10.1555

By:

Rotman, Galit;
Shiloh, Yosef

Publication type:

Article

Gene defect behind APECED: a new clue to autoimmunity.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1547, doi. 10.1093/hmg/7.10.1547

By:

Björses, Petra;
Aaltonen, Johanna;
Horelli-Kuitunen, Nina;
Yaspo, Marie-Laure;
Peltonen, Leena

Publication type:

Article

The genetics of psoriasis: a complex disorder of the skin and immune system.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1537, doi. 10.1093/hmg/7.10.1537

By:

Bhalerao, Jayant;
Bowcock, Anne M.

Publication type:

Article

The role of the SMN gene in proximal spinal muscular atrophy.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 10, p. 1531, doi. 10.1093/hmg/7.10.1531

By:

Lefebvre, Suzie;
Bürglen, Lydie;
Frézal, Jean;
Munnich, Arnold;
Melki, Judith

Publication type:

Article