Works matching IS 10614036 AND DT 2001 AND VI 29 AND IP 2
Results: 32
Stem-cell politics.
- Published in:
- 2001
- Publication type:
- Editorial
Declaring financial interests.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 102, doi. 10.1038/ng1001-102
- Publication type:
- Article
Genetic inroads in familial ALS.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 103, doi. 10.1038/ng1001-103
- By:
- Publication type:
- Article
The promoter connection.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 105, doi. 10.1038/ng1001-105
- By:
- Publication type:
- Article
The adaptable lin-39.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 106, doi. 10.1038/ng1001-106
- By:
- Publication type:
- Article
Time for T.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 107, doi. 10.1038/ng1001-107
- By:
- Publication type:
- Article
Islands of linkage disequilibrium.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 109, doi. 10.1038/ng1001-109
- By:
- Publication type:
- Article
TOUCHINGbase.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 113
- Publication type:
- Article
The misunderstood geneticist.
- Published in:
- 2001
- By:
- Publication type:
- Book Review
TGF-β signaling in tumor suppression and cancer progression.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 117, doi. 10.1038/ng1001-117
- By:
- Publication type:
- Article
Intra-cytoplasmic sperm injection and infertility.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 131, doi. 10.1038/ng1001-131
- By:
- Publication type:
- Article
An SSLP marker?anchored BAC framework map of the mouse genome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 133, doi. 10.1038/ng1001-133
- By:
- Publication type:
- Article
A role for MLH3 in hereditary nonpolyposis colorectal cancer.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 137, doi. 10.1038/ng1001-137
- By:
- Publication type:
- Article
Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 139, doi. 10.1038/ng1001-139
- By:
- Publication type:
- Article
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 160, doi. 10.1038/ng1001-160
- By:
- Publication type:
- Article
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 166, doi. 10.1038/ng1001-166
- By:
- Publication type:
- Article
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 184, doi. 10.1038/ng1001-184
- By:
- Publication type:
- Article
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 189, doi. 10.1038/ng1001-189
- By:
- Publication type:
- Article
A radiation hybrid transcript map of the mouse genome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 194, doi. 10.1038/ng1001-194
- By:
- Publication type:
- Article
A radiation hybrid map of mouse genes.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 201, doi. 10.1038/ng1001-201
- By:
- Publication type:
- Article
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 217, doi. 10.1038/ng1001-217
- By:
- Publication type:
- Article
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 223, doi. 10.1038/ng1001-223
- By:
- Publication type:
- Article
High-resolution haplotype structure in the human genome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 229, doi. 10.1038/ng1001-229
- By:
- Publication type:
- Article
Haplotype tagging for the identification of common disease genes.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 233, doi. 10.1038/ng1001-233
- By:
- Publication type:
- Article
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 134, doi. 10.1038/ng716
- By:
- Publication type:
- Article
Identifying regulatory networks by combinatorial analysis of promoter elements.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 153, doi. 10.1038/ng724
- By:
- Publication type:
- Article
Disruption of Trrap causes early embryonic lethality and defects in cell cycle progression.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 206, doi. 10.1038/ng725
- By:
- Publication type:
- Article
Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 212, doi. 10.1038/ng727
- By:
- Publication type:
- Article
Gene polymorphism in Netherton and common atopic disease.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 175, doi. 10.1038/ng728
- By:
- Publication type:
- Article
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 179, doi. 10.1038/ng730
- By:
- Publication type:
- Article
Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 143, doi. 10.1038/ng731
- By:
- Publication type:
- Article
Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 141, doi. 10.1038/ng740
- By:
- Publication type:
- Article