Volume 17; Issue 2

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Nature Genetics
Volume 17; Issue 2

Nature Genetics

Volume 17; Issue 2

1

Come together

Journal:

Nature Genetics

Year:

1997

File:

PDF, 216 KB

1997

2

Chloride channels cough up

Thakker, Rajesh V.

Journal:

Nature Genetics

Year:

1997

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PDF, 578 KB

1997

3

The maddening hunt for madness genes

Moldin, Steven O.

Journal:

Nature Genetics

Year:

1997

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PDF, 448 KB

1997

4

On the TRAIL from p53 to apoptosis?

Kastan, Michael

Journal:

Nature Genetics

Year:

1997

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PDF, 228 KB

1997

5

A searchlight through the fog

Wright, Alan F.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 431 KB

1997

6

Touching base

Journal:

Nature Genetics

Year:

1997

File:

PDF, 156 KB

1997

7

A human compound heterozygote for two MLH1 missense mutations

Hackman, Peter, Tannergård, Pia, Osei-Mensa, Salome, Chen, Jindong, Kane, Michael F., Kolodner, Richard, Lambert, Bo, Hellgren, Dennis, Lindblom, Annika

Journal:

Nature Genetics

Year:

1997

File:

PDF, 185 KB

1997

8

Sex–dependent rearrangements resulting in CMT1A and HNPP

Lopes, Judith, Vandenberghe, Antoon, Tardieu, Sandrine, lonasescu, Victor, Lévy, Nicolas, Wood, Nicholas, Tachi, Nobutada, Bouche, Pierre, Latour, Philippe, Brice, Alexis

Journal:

Nature Genetics

Year:

1997

File:

PDF, 229 KB

1997

9

Early-onset type-ll diabetes mellitus (MODY4) linked to IPF1

Staffers, Doris A., Ferrer, Jorge, Clarke, William L., Habener, Joel F.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 253 KB

1997

10

Mutations in RPE65 cause Leber's congenital amaurosis

Marlhens, Françoise, Bareil, Corinne, Griffoin, Jean-Michel, Zrenner, Eberhart, Amalric, Pierre, Eliaou, Claudie, Liu, Su-Yan, Harris, Eddie, Redmond, T. Michael, Arnaud, Bernard

Journal:

Nature Genetics

Year:

1997

File:

PDF, 459 KB

1997

11

KILLER/DR5 is a DNA damage–inducible p53–regulated death receptor gene

Wu, Gen Sheng, Burns, Timothy F., McDonald, E. Robert, Jiang, Wen, Meng, Ray, Krantz, Ian D., Kao, Gary, Gan, Dai-Di, Zhou, Jun-Ying, Muschel, Ruth

Journal:

Nature Genetics

Year:

1997

File:

PDF, 530 KB

1997

12

PTEN1 is frequently mutated in primary endometrial carcinomas

Kong, Dehe, Suzuki, Akihiko, Zou, Tong-Tong, Sakurada, Akira, Kemp, Lawrence W., Wakatsuki, Shigeru, Yokoyama, Tadaaki, Yamakawa, Hiromitsu, Furukawa, Toru, Sato, Masami

Journal:

Nature Genetics

Year:

1997

File:

PDF, 354 KB

1997

13

Genetic interaction between HAP1/REF-1 and p53

Meira, Lisiane B., Cheo, David L., Hammer, Robert E., Burns, Dennis K., Reis, Antonio, Friedberg, Errol C.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 133 KB

1997

14

Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain

Gibbons, Richard J., Bachoo, Satvinder, Picketts, David J., Aftimos, Salim, Asenbauer, Bernhard, Bergoffen, JoAnn, Berry, Susan A., Dahl, Niklas, Fryer, Alan, Keppler, Kim

Journal:

Nature Genetics

Year:

1997

File:

PDF, 484 KB

1997

15

Diabetes, dependence, asymptotics, selection and significance

Kong, Augustine, Frigge, Mike, Bell, Graeme I., Lander, Eric S., Daly, Mark J., Cox, Nancy J.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 126 KB

1997

16

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

Hildebrandt, Friedhelm, Otto, Edgar, Rensing, Cornelia, Nothwang, Hans Gerd, Vollmer, Martin, Adolphs, Jörn, Hanusch, Helge, Brandis, Matthias

Journal:

Nature Genetics

Year:

1997

File:

PDF, 576 KB

1997

17

Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

Chen, Ken-Shiung, Manian, Prasad, Koeuth, Thearith, Potocki, Lorraine, Zhao, Qi, Chinault, A. Craig, Lee, Cheng Chi, Lupski, James R.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 1.29 MB

1997

18

Positional cloning of the gene associated with X-linked juvenile retinoschisis

Sauer, Christian G., Gehrig, Andrea, Warneke-Wittstock, Regina, Marquardt, Andreas, Ewing, Cecil C., Gibson, Alice, Lorenz, Birgit, Jurklies, Bernhard, Weber, Bernhard H.F.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 931 KB

1997

19

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Simon, David B., Bindra, Ranjit S., Mansfield, Traci A., Nelson-Williams, Carol, Mendonca, Erica, Stone, Rosário, Schurman, Scott, Nayir, Ahmet, Alpay, Harika, Bakkaloglu, Aysin

Journal:

Nature Genetics

Year:

1997

File:

PDF, 925 KB

1997

20

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

Lu, Weining, Peissel, Bernard, Babakhanlou, Hermik, Pavlova, Anna, Geng, Lin, Fan, Xiaohong, Larson, Cecilia, Brent, Gregory, Zhou, Jing

Journal:

Nature Genetics

Year:

1997

File:

PDF, 502 KB

1997

21

Male–driven evolution of DNA sequences in birds

Ellegren, Hans, Fridolfsson, Anna-Karin

Journal:

Nature Genetics

Year:

1997

File:

PDF, 324 KB

1997

22

Identification of PAHX, a Refsum disease gene

Mihalik, Stephanie J., Morrell, James C., Kim, Do, Sacksteder, Katherine A., Watkins, Paul A., Gould, Stephen J.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 608 KB

1997

23

Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene

Jansen, Gerbert A., Oftnan, Rob, Ferdinandusse, Sacha, Ijlst, Lodewijk, Muijsers, Anton O., Skjeldal, Ola H., Stokke, Oddvar, Jakobs, Cornells, Besley, Guy T.N., Wraith, J. Ed

Journal:

Nature Genetics

Year:

1997

File:

PDF, 485 KB

1997

24

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

Gu, Su-min, Thompson, Debra A., Srikumari, C.R. Srisailapathy, Lorenz, Birgit, Finckh, Ulrich, Nicoletti, Aileen, Murthy, K.R., Rathmann, Michaela, Kumaramanickavel, Govindasamy, Denton, Michael J.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 378 KB

1997

25

Mutation of the gene encoding cellular retinaldehyde–binding protein in autosomal recessive retinitis pigmentosa

Maw, Marion A., Kennedy, Breandan, Knight, Allison, Bridges, Robyn, Roth, Karen E., Mani, E.J., Mukkadan, J.K., Nancarrow, Derek, Crabb, John W., Denton, Michael J.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 393 KB

1997

26

The genetic and functional basis of isolated 17,20–lyase deficiency

Geller, David H., Auchus, Richard J., Mendonça, Berenice B., Miller, Walter L.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 686 KB

1997

27

Increased stress response and β–phenylethylamine in MAOB–deficient mice

Grimsby, Joseph, Toth, Miklos, Chen, Kevin, Kumazawa, Takeshi, Klaidman, Lori, Adams, James D., Karoum, Farouk, Gal, Judit, Shih, Jean C.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 626 KB

1997

28

Drosophila CBP is required for dorsal–dependent twist gene expression

Akimaru, Hiroshi, Hou, De-Xing, Ishii, Shunsuke

Journal:

Nature Genetics

Year:

1997

File:

PDF, 546 KB

1997

29

Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia

Rötig, Agnès, de Lonlay, Pascale, Chretien, Dominique, Foury, Françoise, Koenig, Michel, Sidi, Daniel, Munnich, Arnold, Rustin, Pierre

Journal:

Nature Genetics

Year:

1997

File:

PDF, 345 KB

1997

30

Targetting of the gene encoding fibrillin–1 recapitulates the vascular aspect of Marfan syndrome

Pereira, Lygia, Andrikopoulos, Konstantinos, Tian, Jenny, Lee, Sui Ying, Keene, Douglas R., Ono, Robert, Reinhardt, Dieter P., Sakai, Lynn Y., Biery, Nancy Jensen, Bunton, Tracie

Journal:

Nature Genetics

Year:

1997

File:

PDF, 767 KB

1997

31

Cre–mediated chromosome loss in mice

Lewandoski, Mark, Martin, Gail R.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 407 KB

1997

32

Human telomeres contain two distinct Myb–related proteins, TRF1 and TRF2

Broccoli, Dominique, Smogorzewska, Agata, Chong, Laura, de Lange, Titia

Journal:

Nature Genetics

Year:

1997

File:

PDF, 731 KB

1997

33

Telomeric localization of TRF2, a novel human telobox protein

Bilaud, Thomas, Brun, Christine, Ancelin, Katia, Koering, Catherine Elaine, Laroche, Thierry, Gilson, Eric

Journal:

Nature Genetics

Year:

1997

File:

PDF, 535 KB

1997

34

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

McGrath, John A., McMillan, James R., Shemanko, Carrie S., Runswick, Sarah K., Leigh, Irene M., Lane, E. Birgitte, Garrod, David R., Eady, Robin A.J.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 813 KB

1997

35

Autumn days, purple haze

Journal:

Nature Genetics

Year:

1997

File:

PDF, 225 KB

1997

36

Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma

Iida, Shinsuke, Rao, Pulivarthi H., Butler, Marion, Corradini, Paolo, Boccadoro, Mario, Klein, Bernard, Chaganti, R.S.K., Dalla-Favera, Riccardo

Journal:

Nature Genetics

Year:

1997

File:

PDF, 668 KB

1997

37

Molecular evolution—who is in the driver's seat?

Journal:

Nature Genetics

Year:

1997

File:

PDF, 265 KB

1997

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