Works matching IS 10614036 AND DT 2001 AND VI 27 AND IP 4

Results: 24

All hands on deck at dawn.

Published in:: Nature Genetics, 2001, v. 27, n. 4, p. 347, doi. 10.1038/86818
Publication type:: Article

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 367, doi. 10.1038/86856

By:

Charlier, Carole;
Segers, Karin;
Karim, Latifa;
Shay, Tracy;
Gyapay, Gabor;
Cockett, Noelle;
Georges, Michel

Publication type:

Article

Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 392, doi. 10.1038/86891

By:

Zenklusen, Jean C.;
Conti, Claudio J.;
Green, Eric D.

Publication type:

Article

How does the mouse get its trunk?

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 351, doi. 10.1038/86829

By:

Dunn, N Ray;
Hogan, Brigid L M

Publication type:

Article

Fanconi anemia and breast cancer: what's the connection?

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 352, doi. 10.1038/86832

By:

Youssoufian, Hagop

Publication type:

Article

A particular GAP in mind.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 354, doi. 10.1038/86835

By:

Zhu, Yuan;
Parada, Luis F

Publication type:

Article

The pancreas and its heartless beginnings.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 355, doi. 10.1038/86839

By:

Duncan, Stephen A

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 2001, v. 27, n. 4, p. 357
Publication type:: Article

Yesterday's news.

Published in:

2001

By:

McGee, Glenn

Publication type:

Book Review

Retrotransposons as epigenetic mediators of phenotypic variation in mammals.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 361, doi. 10.1038/86850

By:

Whitelaw, Emma;
Martin, David I.K.

Publication type:

Article

Single-nucleotide polymorphisms in the public domain: how useful are they?

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 371, doi. 10.1038/86864

By:

Marth, Gabor;
Yeh, Raymond;
Minton, Matthew;
Donaldson, Rachel;
Li, Qun;
Duan, Shenghui;
Davenport, Ruth;
Miller, Raymond D.;
Kwok, Pui-Yan

Publication type:

Article

Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 372, doi. 10.1038/86867

By:

Cookson, William O.C.M.;
Ubhi, Baljinder;
Lawrence, Robert;
Abecasis, Gonçalo R.;
Walley, Andrew J.;
Cox, Helen E.;
Coleman, Rosemary;
Leaves, Nicholas I.;
Trembath, Richard C.;
Moffatt, Miriam F.;
Harper, John I.

Publication type:

Article

Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 369, doi. 10.1038/86860

By:

Wakamatsu, Nobuaki;
Yamada, Yasukazu;
Yamada, Kenichiro;
Ono, Takao;
Nomura, Noriko;
Taniguchi, Hiroko;
Kitoh, Hiroshi;
Mutoh, Norihiro;
Yamanaka, Tsutomu;
Mushiake, Kyosuke;
Kato, Kanefusa;
Sonta, Shin-ichi;
Nagaya, Masahiro

Publication type:

Article

Trinucleotide expansion in haploid germ cells by gap repair.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 407, doi. 10.1038/86906

By:

Kovtun, Irina V.;
McMurray, Cynthia T.

Publication type:

Article

A major susceptibility locus for leprosy in India maps to chromosome 10p13.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 439, doi. 10.1038/86958

By:

Siddiqui, M. Ruby;
Meisner, Sarah;
Tosh, Kerrie;
Balakrishnan, Karuppiah;
Ghei, Satish;
Fisher, Simon E.;
Golding, Marina;
Shanker Narayan, Nallakandy P.;
Sitaraman, Thiagarajan;
Sengupta, Utpal;
Pitchappan, Ramasamy;
Hill, Adrian V.S.

Publication type:

Article

Hepatocyte nuclear factor-1α is an essential regulator of bile acid and plasma cholesterol metabolism.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 375, doi. 10.1038/86871

By:

Shih, David Q.;
Bussen, Markus;
Sehayek, Ephraim;
Ananthanarayanan, Meenakshisundaram;
Shneider, Benjamin L.;
Suchy, Frederick J.;
Shefer, Sarah;
Bollileni, Jaya S.;
Gonzalez, Frank J.;
Breslow, Jan L.;
Stoffel, Markus

Publication type:

Article

Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 383, doi. 10.1038/86882

By:

Kuehl, Peter;
Zhang, Jiong;
Lin, Yvonne;
Lamba, Jatinder;
Assem, Mahfoud;
Schuetz, John;
Watkins, Paul B.;
Daly, Ann;
Wrighton, Steven A.;
Hall, Stephen D.;
Maurel, Patrick;
Relling, Mary;
Brimer, Cynthia;
Yasuda, Kazuto;
Venkataramanan, Raman;
Strom, Stephen;
Thummel, Kenneth;
Boguski, Mark S.;
Schuetz, Erin

Publication type:

Article

Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 399, doi. 10.1038/86898

By:

Costa, Rui M.;
Yang, Tao;
Huynh, Duong P.;
Pulst, Stefan M.;
Viskochil, David H.;
Silva, Alcino J.;
Brannan, Camilynn I.

Publication type:

Article

The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm?specific protein with an extracellular cysteine-rich domain.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 412, doi. 10.1038/86912

By:

Kalantry, Sundeep;
Manning, Sharon;
Haub, Olivia;
Tomihara-Newberger, Carol;
Lee, Hong-Gee;
Fangman, Jennifer;
Disteche, Christine M.;
Manova, Katia;
Lacy, Elizabeth

Publication type:

Article

An alternative mode of translation permits production of a variant NBS1 protein from the common Nijmegen breakage syndrome allele.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 417, doi. 10.1038/86920

By:

Maser, Richard S.;
Zinkel, Robert;
Petrini, John H.J.

Publication type:

Article

An abundance of X-linked genes expressed in spermatogonia.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 422, doi. 10.1038/86927

By:

Wang, P. Jeremy;
McCarrey, John R.;
Yang, Fang;
Page, David C.

Publication type:

Article

TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 427, doi. 10.1038/86934

By:

Kuramochi, Masami;
Fukuhara, Hiroshi;
Nobukuni, Takahiro;
Kanbe, Takamasa;
Maruyama, Tomoko;
Ghosh, Hara P.;
Pletcher, Mathew;
Isomura, Minoru;
Onizuka, Masataka;
Kitamura, Tadaichi;
Sekiya, Takao;
Reeves, Roger H.;
Murakami, Yoshinori

Publication type:

Article

Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 431, doi. 10.1038/86941

By:

Arikawa-Hirasawa, Eri;
Wilcox, William R.;
Le, Alexander H.;
Silverman, Neil;
Govindraj, Prasanthi;
Hassell, John R.;
Yamada, Yoshihiko

Publication type:

Article

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.

Published in:

Nature Genetics, 2001, v. 27, n. 4, p. 435, doi. 10.1038/86948

By:

Glatt, Charles E.;
DeYoung, Joseph A.;
Delgado, Sharon;
Service, Susan K.;
Giacomini, Kathleen M.;
Edwards, Robert H.;
Risch, Neil;
Freimer, Nelson B.

Publication type:

Article