Why are some human disease-associated mutations fixed in mice?

By Gao L.   Zhang J.  

Trends in Genetics, Vol. 19, Iss. 12, 2003-12 ,pp. : 678-681

Elsevier

Access to resources Recommend Favorite

Absence of MEN2A- or 2B-type RET mutations in primary neuroblastoma tumour tissue

By Peaston A.E.   Camacho M.L.   Norris M.D.   Haber M.   Marsh D.J.   Robinson B.G.   Hyland V.J.   Marshall G.M.  

Molecular and Cellular Probes, Vol. 12, Iss. 4, 1998-08 ,pp. : 239-242

Academic Press

Access to resources Recommend Favorite

Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease

By Odermatt A.   Taschner P.E.M.   Scherer S.W.   Beatty B.   Khanna V.K.   Cornblath D.R.   Chaudhry V.   Yee W.C.   Schrank B.   Karpati G.   Breuning M.H.   Knoers N.   Maclennan D.H.  

Genomics, Vol. 45, Iss. 3, 1997-11 ,pp. : 541-553

Academic Press

Access to resources Recommend Favorite

Distribution of GDNF family receptor α3 and RET in rat and human non-neural tissues

By Yang Chunhua   Hutto David   Sah Dinah  

Journal of Molecular Histology, Vol. 37, Iss. 1-2, 2006-01 ,pp. : 69-77

Springer Publishing Company

Access to resources Recommend Favorite

Efficient Detection of Mutations in Wilson Disease by Manifold Sequencing

By Waldenstrom E.   Lagerkvist A.   Dahlman T.   Westermark K.   Landegren U.  

Genomics, Vol. 37, Iss. 3, 1996-11 ,pp. : 303-309

Academic Press

Access to resources Recommend Favorite