Lane PW - Search Results

1

Downeast anemia (dea), a new mouse model of severe nonspherocytic hemolytic anemia caused by hexokinase (HK(1)) deficiency.

Peters LL, Lane PW, Andersen SG, Gwynn B, Barker JE, Beutler E. Peters LL, et al. Among authors: lane pw. Blood Cells Mol Dis. 2001 Sep-Oct;27(5):850-60. doi: 10.1006/bcmd.2001.0454. Blood Cells Mol Dis. 2001. PMID: 11783948

2

Mouse models of genetic diseases.

Leiter EH, Beamer WG, Shultz LD, Barker JE, Lane PW. Leiter EH, et al. Among authors: lane pw. Birth Defects Orig Artic Ser. 1987;23(3):221-57. Birth Defects Orig Artic Ser. 1987. PMID: 3307936 Review. No abstract available.

3

The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia.

Chase TH, Lyons BL, Bronson RT, Foreman O, Donahue LR, Burzenski LM, Gott B, Lane P, Harris B, Ceglarek U, Thiery J, Wittenburg H, Thon JN, Italiano JE Jr, Johnson KR, Shultz LD. Chase TH, et al. Blood. 2010 Feb 11;115(6):1267-76. doi: 10.1182/blood-2009-05-219808. Epub 2009 Oct 21. Blood. 2010. PMID: 19846887 Free PMC article.

4

Juvenile bare: a new hair loss mutation on chromosome 7 of the mouse.

Lane PW, Bronson RT, Cook SA, Ward-Bailey P, Donahue LR, Davisson MT. Lane PW, et al. J Hered. 1998 May-Jun;89(3):254-7. doi: 10.1093/jhered/89.3.254. J Hered. 1998. PMID: 9656467

5

Hairpatches, a single gene mutation characterized by progressive renal disease and alopecia in the mouse. A potential model for a newly described heritable human disorder.

Shultz LD, Lane PW, Coman DR, Taylor S, Hall E, Lyons B, Wood BG, Schlager G. Shultz LD, et al. Among authors: lane pw. Lab Invest. 1991 Nov;65(5):588-600. Lab Invest. 1991. PMID: 1836514

6

Rostral cerebellar malformation, (rcm): a new recessive mutation on chromosome 3 of the mouse.

Lane PW, Bronson RT, Spencer CA. Lane PW, et al. J Hered. 1992 Jul-Aug;83(4):315-8. doi: 10.1093/oxfordjournals.jhered.a111221. J Hered. 1992. PMID: 1401878

7

Hydrocephalus with hop gait (hyh): a new mutation on chromosome 7 in the mouse.

Bronson RT, Lane PW. Bronson RT, et al. Among authors: lane pw. Brain Res Dev Brain Res. 1990 Jun 1;54(1):131-6. doi: 10.1016/0165-3806(90)90073-8. Brain Res Dev Brain Res. 1990. PMID: 2364541

8

New mutation causing sterility in the mouse.

Handel MA, Lane PW, Schroeder AC, Davisson MT. Handel MA, et al. Among authors: lane pw. Gamete Res. 1988 Dec;21(4):409-23. doi: 10.1002/mrd.1120210409. Gamete Res. 1988. PMID: 3220432

9

Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac.

Johnson KR, Lane PW, Ward-Bailey P, Davisson MT. Johnson KR, et al. Among authors: lane pw. Genomics. 1995 Sep 20;29(2):457-64. doi: 10.1006/geno.1995.9981. Genomics. 1995. PMID: 8666395

10

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.

Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, Faust JR. Bronson RT, et al. Among authors: lane pw. Am J Med Genet. 1998 May 26;77(4):289-97. doi: 10.1002/(sici)1096-8628(19980526)77:4<289::aid-ajmg8>3.0.co;2-i. Am J Med Genet. 1998. PMID: 9600738

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