Volume 16; Issue 3

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Nature Genetics
Volume 16; Issue 3

Nature Genetics

Volume 16; Issue 3

1

The internet strikes back

Journal:

Nature Genetics

Year:

1997

File:

PDF, 217 KB

1997

2

A celebration and a farewell

Goodfellow, Peter

Journal:

Nature Genetics

Year:

1997

File:

PDF, 254 KB

1997

3

Breast cancer genes—what are the real risks?

Journal:

Nature Genetics

Year:

1997

File:

PDF, 282 KB

1997

4

Alagille syndrome—a notch up for the Notch receptor

Artavanis-Tsakonas, Spyros

Journal:

Nature Genetics

Year:

1997

File:

PDF, 316 KB

1997

5

Raf revealed in life-or-death decisions

Pritchard, Catrin, McMahon, Martin

Journal:

Nature Genetics

Year:

1997

File:

PDF, 306 KB

1997

6

Looms to weave genomic nets

Journal:

Nature Genetics

Year:

1997

File:

PDF, 327 KB

1997

7

FISH with a twist

Lizardi, Paul M., Ward, David C.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 232 KB

1997

8

And finally, genes for human obesity

Leibel, Rudolph L.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 617 KB

1997

9

Touching base

Journal:

Nature Genetics

Year:

1997

File:

PDF, 142 KB

1997

10

The extent of genetic variation in the CCR5 gene

Ansari-Lari, M. Ali, Liu, Xiao-Mei, Metzker, Michael L., Rut, Andrew R., Gibbs, Richard A.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 439 KB

1997

11

Reversal of a mitochondrial DNA defect in human skeletal muscle

Clark, Kim M., Bindoff, Laurence A., Lightowlers, Robert N., Andrews, Richard M., Griffiths, Philip G., Johnson, Margaret A., Brierley, Elizabeth J., Turnbull, Douglass M.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 412 KB

1997

12

Deletion of the promoter region in the Atp7a gene of the mottled dappled mouse

Levinson, Barbara, Packman, Seymour, Gitschier, Jane

Journal:

Nature Genetics

Year:

1997

File:

PDF, 194 KB

1997

13

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

Graham, Brett H., Waymire, Katrina G., Cottrell, Barbara, Trounce, Ian A., MacGregor, Grant R., Wallace, Douglas C.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.28 MB

1997

14

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Spinner, Nancy B., Collins, Francis S., Oda, Takaya, Elkahloun, Abdel G., Pike, Brian L., Okajima, Kazuki, Krantz, Ian D., Genin, Anna, Piccoli, David A., Meltzer, Paul S.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 941 KB

1997

15

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

Li, Linheng, Krantz, Ian D., Deng, Yu, Genin, Anna, Banta, Amy B., Collins, Colin C., Qi, Ming, Trask, Barbara J., Kuo, Wen Lin, Cochran, Joanne

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.25 MB

1997

16

Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21

Nilsson, Mats, Krejci, Katerina, Koch, Jørn, Kwiatkowski, Marek, Gustavsson, Peter, Landegren, Ulf

Journal:

Nature Genetics

Year:

1997

File:

PDF, 394 KB

1997

17

A component of the transcriptional represser MeCP1 shares a motif with DNA methyltransferase and HRX proteins

Cross, Sally H., Meehan, Richard R., Nan, Xinsheng, Bird, Adrian

Journal:

Nature Genetics

Year:

1997

File:

PDF, 598 KB

1997

18

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

Chesi, Marta, Nardini, Elena, Brents, Leslie A., Schröck, Evelin, Ried, Thomas, Kuehl, W. Michael, Bergsagel, P. Leif

Journal:

Nature Genetics

Year:

1997

File:

PDF, 592 KB

1997

19

Correlation between severity and SMN protein level in spinal muscular atrophy

Lefebvre, Suzie, Burlet, Philippe, Liu, Qing, Bertrandy, Solange, Clermont, Olivier, Munnich, Arnold, Dreyfuss, Gideon, Melki, Judith

Journal:

Nature Genetics

Year:

1997

File:

PDF, 636 KB

1997

20

Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors

Snyder, Richard O., Miao, Carol H., Patijn, Gijsbert A., Spratt, S. Kaye, Danos, Olivier, Nagy, Dea, Gown, Allen M., Winther, Brian, Meuse, Leonard, Cohen, Lawrence K.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 911 KB

1997

21

Toward a functional analysis of the yeast genome through exhaustive two-hybrid screens

Fromont-Racine, Micheline, Rain, Jean-Christophe, Legrain, Pierre

Journal:

Nature Genetics

Year:

1997

File:

PDF, 920 KB

1997

22

Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in Drosophila

Cohen, Brenda, Bashirullah, Arash, Dagnino, Lina, Campbell, Christine, Fisher, William W., Leow, Ching Ching, Whiting, Elisabeth, Ryan, David, Zinyk, Dawn, Boulianne, Gabrielle

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.02 MB

1997

23

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

Pastural, Elodie, Barrat, Franck J., Dufourcq-Lagelouse, Rémi, Certain, Stéphanie, Sanal, Ozden, Jabado, Nada, Seger, Reinhard, Griscelli, Claude, Fischer, Alain, Basile, Geneviève de Saint

Journal:

Nature Genetics

Year:

1997

File:

PDF, 471 KB

1997

24

Endothelial apoptosis in Braf-deficient mice

Wojnowski, Leszek, Zimmer, Anne M., Beck, Thomas W., Hahn, Heidi, Bernal, Ricardo, Rapp, Ulf R., Zimmer, Andreas

Journal:

Nature Genetics

Year:

1997

File:

PDF, 887 KB

1997

25

Partial rescue of Brca15–6 early embryonic lethality by p53 or p21 null mutation

Hakem, Razqallah, de la Pompa, José Luis, Elia, Andrew, Potter, Julia, Mak, Tak W.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 672 KB

1997

26

Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

Raffin-Sanson, Marie-Laure, Sanders, Louise, Montague, Carl T., Hutton, John C., O'Rahilly, Stephen, Jackson, Robert S., Creemers, John W.M., Ohagi, Shinya

Journal:

Nature Genetics

Year:

1997

File:

PDF, 517 KB

1997

27

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia

Lee, Brendan, Thirunavukkarasu, Kannan, Zhou, Lei, Pastore, Lucio, Baldini, Antonio, Hecht, Jacqueline, Geoffrey, Valeric, Ducy, Patricia, Karsenty, Gerard

Journal:

Nature Genetics

Year:

1997

File:

PDF, 575 KB

1997

28

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

Bamshad, Michael, Lin, Robert C., Law, David J., Watkins, W. Scott, Krakowiak, Patrycja A., Moore, Mary E., Franceschini, Piergiorgio, Lala, Roberto, Holmes, Lewis B., Gebuhr, Tom C.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 726 KB

1997

29

Corrigendum: Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Journal:

Nature Genetics

Year:

1997

File:

PDF, 102 KB

1997

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