Volume 10; Issue 3

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Nature Genetics
Volume 10; Issue 3

Nature Genetics

Volume 10; Issue 3

1

Genetics meets the press

Journal:

Nature Genetics

Year:

1995

File:

PDF, 241 KB

1995

2

Size is important, but…

Oliver, Stephen

Journal:

Nature Genetics

Year:

1995

File:

PDF, 294 KB

1995

3

Slippery DNA runs on and on and on…

Journal:

Nature Genetics

Year:

1995

File:

PDF, 330 KB

1995

4

CATCHing a break on 22

Glover, Thomas W.

Journal:

Nature Genetics

Year:

1995

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PDF, 220 KB

1995

5

How neutral are synonymous codon mutations?

Richard, Isabella, Beckmann, Jacques S.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 99 KB

1995

6

Atopy in Australia

Duffy, David L., Healey, Sue C., Chenevix-Trench, Georgia, Martin, Nick G., Weger, John, Lichter, Jay

Journal:

Nature Genetics

Year:

1995

File:

PDF, 114 KB

1995

7

Reply to “Atopy in Australia”

Hill, Michael R., Cookson, William O.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 114 KB

1995

8

Analysis of the nucleotide sequence of chromosome VI from Saccharomyces cerevisiae

Murakami, Yasufumi, Naitou, Masanori, Hagiwara, Hiroko, Shibata, Takehiko, Ozawa, Masashi, Sasanuma, Syun-ichi, Sasanuma, Motoe, Tsuchiya, Yukari, Soeda, Eiichi, Yokoyama, Kazushige

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.26 MB

1995

9

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

Bailey, L. Charles, Sellinger, Bea, Michaud, Dominique, Driscoll, Deborah A., Emanuel, Beverly S., Budarf, Marcia L., Collins, Joelle, Gong, Weilong, Roe, Bruce, Wang, Zhili

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.26 MB

1995

10

Adenosine–deaminase–deficient mice die perinatally and exhibit liver–cell degeneration, atelectasis and small intestinal cell death

Migchielsen, Alexandra A.J., Breuer, Marco L., van Roon, Marian A., Riele, Hein te, Zurcher, Chris, Ossendorp, Ferry, Toutain, Stephan, Hershfield, Michael S., Berns, Anton, Valerio, Dinko

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.32 MB

1995

11

Acid sphingomyelinase deficient mice: a model of types A and B Niemann–Pick disease

Horinouchi, Kenichi, Erlich, Shai, Perl, Daniel P., Ferlinz, Klaus, Bisgaier, Charles L., Sandhoff, Konrad, Desnick, Robert J., Stewart, Colin L., Schuchman, Edward H.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 848 KB

1995

12

The Grb2 binding domain of mSos1 is not required for downstream signal transduction

Wang, Wei, Fisher, Elizabeth M.C., Jia, Qi, Dunn, James M., Porfiri, Emilio, Downward, Julian, Egan, Sean E.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.15 MB

1995

13

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1

Brown, Arthur, Bernier, Gilbert, Mathieu, Martine, Rossant, Janet, Kothary, Rashmi

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.06 MB

1995

14

Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts

Stambolian, Dwight, Ai, Yunjun, Sidjanin, Duska, Nesburn, Kristin, Sathe, Ganesh, Rosenberg, Martin, Bergsma, Derk J.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 732 KB

1995

15

Identification of murine loci associated with susceptibility to chronic experimental autoimmune encephalomyelitis

Sundvall, Mats, Jirholt, Johan, Yang, Hai-Tao, Jansson, Liselotte, Engström, Åke, Pettersson, Ulf, Holmdahl, Rikard

Journal:

Nature Genetics

Year:

1995

File:

PDF, 511 KB

1995

16

Establishment of functional imprinting of the H19 gene in human developing placentae

Jinno, Yoshihiro, Ikeda, Yuichiro, Yun, Kankatsu, Maw, Marion, Masuzaki, Hideaki, Fukuda, Hisanobu, Inuzuka, Kunihiko, Fujishita, Akira, Ohtani, Yoshinobu, Okimoto, Tomoaki

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.22 MB

1995

17

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

Hecht, Jacqueline T., Nelson, Laura D., Crowder, Eric, Wang, Yang, Elder, Frederick F.B., Harrison, Wilbur R., Francomano, Clair A., Prange, Christa K., Lennon, Gregory G., Deere, Michelle

Journal:

Nature Genetics

Year:

1995

File:

PDF, 577 KB

1995

18

Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene

Briggs, M.D., Hoffman, S.M.G., King, L.M., Olsen, A.S., Mohrenweiser, H., Leroy, J.G., Mortier, G.R., Rimoin, D.L., Lachman, R.S., Gaines, E.S.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 853 KB

1995

19

Microsatellite evolution — evidence for directionality and variation in rate between species

Rubinsztein, David C., Amos, William, Leggo, Jayne, Goodburn, Sandy, Jain, Sanjeev, Li, Shi-Hua, Margolis, Russell L., Ross, Christopher A., Ferguson-Smith, Malcolm A.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 614 KB

1995

20

Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1

Chong, Samuel S., McCall, Alanna E., Cota, Juan, Subramony, S.H., Orr, Harry T., Hughes, Mark R., Zoghbi, Huda Y.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 1.29 MB

1995

21

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

Gruis, Nelleke A., van der Velden, Pieter A., Sandkuijl, Lodewijk A., Prins, Duncan E., Weaver-Feldhaus, Jane, Kamb, Alexander, Bergman, Wilma, Frants, Rune R.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 310 KB

1995

22

Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q

Eiberg, Hans, Berendt, Ida, Mohr, Jan

Journal:

Nature Genetics

Year:

1995

File:

PDF, 362 KB

1995

23

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

Bellus, Gary A., McIntosh, Iain, Smith, E. Anne, Aylsworth, Arthur S., Kaitila, Ilkka, Horton, William A., Greenhaw, Giselle A., Hecht, Jacqueline T., Francomano, Clair A.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 473 KB

1995

24

A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

Fuchs, Sigrid, Nakazawa, Mitsuru, Maw, Marion, Tamai, Makoto, Oguchi, Yoshihisa, Gal, Andreas

Journal:

Nature Genetics

Year:

1995

File:

PDF, 358 KB

1995

25

Mutation of a type II keratin gene (K6a) in pachyonychia congenita

Bowden, Paul E., Haley, Joanne L., Kansky, Aleksej, Rothnagel, Joseph A., Jones, David O., Turner, Richard J.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 652 KB

1995

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