Point-Mutation, page 10

Search results for Point-Mutation

Found 5318 articles. Showing from 91 to 100.

American journal of medical genetics. Part A (2007-12-06)
Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene.

Molecular and cellular biology (2012-08-06)
A distinct Smoothened mutation causes severe cerebellar developmental defects and medulloblastoma in a novel transgenic mouse model.

Brain (2000-06-06)
Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot-Marie-Tooth type 1A.

Cell host & microbe (2008-03-03)
Mutation in the transcriptional regulator PhoP contributes to avirulence of Mycobacterium tuberculosis H37Ra strain.

Journal of bone and mineral research (2012-04-02)
A Phex mutation in a murine model of X-linked hypophosphatemia alters phosphate responsiveness of bone cells.

The Laryngoscope (2011-07-27)
Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients?

British journal of haematology (2010-12-23)
Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects.

Molecular endocrinology (1998-02-10)
A transcriptional silencing domain in DAX-1 whose mutation causes adrenal hypoplasia congenita.

Oncogene (2005-06-30)
A mutation hotspot at the p14ARF splice site.

AIDS (2007-09-21)
The presence of the Trim5alpha escape mutation H87Q in the capsid of late stage HIV-1 variants is preceded by a prolonged asymptomatic infection phase.

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