Found: 15
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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 296, doi. 10.1038/15472
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- Article
An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi.
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- Molecular Microbiology, 2003, v. 47, n. 6, p. 1495, doi. 10.1046/j.1365-2958.2003.03381.x
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- Article
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.
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- Nature, 1987, v. 328, n. 6126, p. 168, doi. 10.1038/328168a0
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- Article
Genetic linkage of Meleda disease to chromosome 8qter.
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- European Journal of Human Genetics, 1998, v. 6, n. 6, p. 542, doi. 10.1038/sj.ejhg.5200254
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- Article
Genome-enabled phylogenetic and functional reconstruction of an araphid pennate diatom Plagiostriata sp. CCMP470, previously assigned as a radial centric diatom, and its bacterial commensal.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65941-x
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- Article
The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis.
- Published in:
- Nucleic Acids Research, 2001, v. 29, n. 10, p. 2145, doi. 10.1093/nar/29.10.2145
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- Article
The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis.
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- Nucleic Acids Research, 2001, v. 29, n. 10, p. 2145, doi. 10.1093/nar/29.10.2145
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- Article
The DNA sequence and analysis of human chromosome 14.
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- Nature, 2003, v. 421, n. 6923, p. 601, doi. 10.1038/nature01348
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- Article
A physical map of human chromosome 14.
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- Nature, 2001, v. 409, n. 6822, p. 947, doi. 10.1038/35057177
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- Article
Mutations in <i>CERS3</i> Cause Autosomal Recessive Congenital Ichthyosis in Humans.
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- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003536
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- Article
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
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- Human Molecular Genetics, 2003, v. 12, n. 18, p. 2369, doi. 10.1093/hmg/ddg235
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- Article
Mutations in the gene encoding SLURP-1 in Mal de Meleda.
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- Human Molecular Genetics, 2001, v. 10, n. 8, p. 875, doi. 10.1093/hmg/10.8.875
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- Article
A Novel Gene that Encodes a Protein with a Putative src Homology 3 Domain is a Candidate Gene for Familial Juvenile Nephronophthisis.
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- Human Molecular Genetics, 1997, v. 6, n. 13, p. 2317, doi. 10.1093/hmg/6.13.2317
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- Article
Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1.
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- Human Molecular Genetics, 1997, v. 6, n. 13, p. 2247, doi. 10.1093/hmg/6.13.2247
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- Article
Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.
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- Human Molecular Genetics, 1995, v. 4, n. 12, p. 2373
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- Article