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Scholar Results 1 - 10 of about 32 citing Sellick: A novel gene for neonatal diabetes maps to chromosome 10p12. 1-p13. (0.09 sec) 

Dynamic model based algorithms for screening and genotyping over 100K SNPs on …

- oxfordjournals.org
X Di, H Matsuzaki, TA Webster, E Hubbell, G … - Bioinformatics, 2005 - Oxford Univ Press
Motivation: A high density of single nucleotide polymorphism (SNP) coverage on
the genome is desirable and often an essential requirement for population
genetics studies. Region-specific or chromosome-specific linkage studies ...
Cited by 101 - Related articles - All 13 versions

Mutations in PTF1A cause pancreatic and cerebellar agenesis


GS Sellick, KT Barker, I Stolte-Dijkstra, C … - Nature genetics, 2004 - nature.com
Cited by 91 - Related articles - BL Direct - All 5 versions

Type 2 diabetes mellitus: not quite exciting enough?

- oxfordjournals.org
F Ashcroft, P Rorsman - Human molecular genetics, 2004 - Oxford Univ Press
Type 2 diabetes mellitus is a serious metabolic disease that afflicts around 5%
of the population in Western societies and over 150 million people worldwide. It
is characterized by elevation of the blood glucose concentration, usually ...
Cited by 70 - Related articles - All 5 versions

Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum

- cell.com
M Hoshino, S Nakamura, K Mori, T Kawauchi, … - Neuron, 2005 - Elsevier
The molecular machinery governing glutamatergic-GABAergic neuronal subtype
specification is unclear. Here we describe a cerebellar mutant, cerebelless,
which lacks the entire cerebellar cortex in adults. The primary defect of ...
Cited by 65 - Related articles - All 5 versions

Genome-wide association study in esophageal cancer using GeneChip mapping 10K array

- aacrjournals.org
N Hu, C Wang, Y Hu, HH Yang, C Giffen, ZZ … - Cancer research, 2005 - AACR
Whole genome association studies of complex human diseases represent a new
paradigm in the postgenomic era. In this study, we report application of the
Affymetrix, Inc. (Santa Clara, CA) high-density single nucleotide ...
Cited by 56 - Related articles - All 6 versions

Mutations in the Kir6. 2 subunit of the KATP channel and permanent neonatal diabetes: new …


AS Slingerland, AT Hattersley - Annals of Medicine, 2005 - informahealthcare.com
Abstract Permanent neonatal diabetes (PNDM) is diagnosed in the first three
months of life and is a major management problem as patients require lifelong
insulin injections. Recently, activating mutations in the KCNJ11 gene which ...
Cited by 43 - Related articles - All 7 versions

Using high-throughput SNP technologies to study cancer


LJ Engle, CL Simpson, JE Landers - Oncogene, 2006 - nature.com
Identifying genes involved in the development of cancer is crucial to fully
understanding cancer biology, for developing novel therapeutics for cancer
treatment and for providing methods for cancer prevention and early ...
Cited by 42 - Related articles - BL Direct - All 4 versions

Proportioning Whole-Genome Single-Nucleotide–Polymorphism Diversity for the …

- stlr.org [PDF] 
O Lao, K Duijn, P Kersbergen, P Knijff, M … - The American Journal of Human Genetics, 2006 - Elsevier
The identification of geographic population structure and genetic ancestry on
the basis of a minimal set of genetic markers is desirable for a wide range of
applications in medical and forensic sciences. However, the absence of ...
Cited by 40 - Related articles - BL Direct - All 14 versions

The Role of Voltage-Gated Calcium Channels in Pancreatic {beta}-Cell Physiology and …

- endojournals.org
SN Yang, PO Berggren - Endocrine reviews, 2006 - Endocrine Soc
Voltage-gated calcium (Ca V ) channels are ubiquitously expressed in various
cell types throughout the body. In principle, the molecular identity,
biophysical profile, and pharmacological property of Ca V channels are ...
Cited by 34 - Related articles - BL Direct - All 6 versions

A new method for autozygosity mapping using single nucleotide polymorphisms (SNPs) …

- bmj.com [PDF] 
CG Woods, EM Valente, J Bond, E Roberts - British Medical Journal, 2004 - jmg.bmj.com
Page 1. doi:10.1136/jmg.2003.016873 2004;41;e101 J. Med. Genet. CG Woods,
EM Valente, J Bond and E Roberts AR XCLUDE single nucleotide ...
Cited by 31 - Related articles - All 5 versions


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