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1. Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader–Willi syndrome mouse models

   Prader–Willi syndrome (PWS) is a neurobehavioral disorder caused by the lack of paternal expression of imprinted genes in the human chromosome region...

   Feng Ding, Yelena Prints, ... Uta Francke in Mammalian Genome

   Article 01 June 2005
   

2. cDNA2Genome: A tool for map** and annotating cDNAs

   Background

   In the last years several high-throughput cDNA sequencing projects have been funded worldwide with the aim of identifying and...

   Coral del Val, Karl-Heinz Glatting, Sandor Suhai in BMC Bioinformatics

   Article Open access 10 September 2003
   

3. Candidate gene polymorphisms among North Indians and their association with schizophrenia in a case-control study

   Knowledge of candidate gene polymorphisms in a population is useful for a variety of gene-disease association studies, particularly for some complex...

   Prachi Semwal, Suman Prasad, ... B. K. Thelma in Journal of Genetics

   Article 01 August 2002

4. List of transgenic and knockout mice: behavioral profiles

   A list of transgenic and knockout mice, having behavioral profiles, has been compiled. Behavioral and genetic information has been assembled in a...

   Valerie Bolivar, Melloni Cook, Lorraine Flaherty in Mammalian Genome

   Article 01 April 2000

5. Mouse chromosome X

   Yvonne Boyd, Helen J. Blair, ... Gail E. Herman in Mammalian Genome

   Article 01 December 1998

6. Master locus list

   in Mammalian Genome

   Article 01 December 1998

7. New seizure frequency QTL and the complex genetics of epilepsy in EL mice

   EL/Suz (EL) mice experience recurrent seizures that are similar to common partial complex epilepsy in humans. In the mice, seizures occur naturally...

   W. N. Frankel, A. Valenzuela, ... J. M. Coffin in Mammalian Genome

   Article 01 December 1995