P. Lane

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

R. Bronson, P. Lane, Roderick T. Bronson, 1990, Brain research. Developmental brain research.

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

M. Davisson, K. Johnson, P. Lane, 1995, Genomics.

Association of megacolon with two recessive spotting genes in the mouse.

P. Lane, 1966, The Journal of heredity.

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

L. Donahue, R. Bronson, K. Johnson, 1998, American journal of medical genetics.

A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse.

P. Lane, M. Deol, 1966, Journal of embryology and experimental morphology.

Association of megacolon with a new dominant spotting gene (Dom) in the mouse.

P. Lane, H. Liu, H. M. Liu, 1984, The Journal of heredity.

The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL/KsJ and C57BL/6J strains

K. Hummel, D. Coleman, P. Lane, 1972, Biochemical Genetics.

Vibrator (vb): a spinocerebellar system degeneration with autosomal recessive inheritance in mice

R. Sidman, P. Lane, W. Weimar, 1982, Brain Research.

Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.

R. Bronson, K. Johnson, M. Davisson, 2003, Genomics.

Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.

A. Ashworth, N. Arnheim, M. Davisson, 1998, Genomics.

Myodystrophy, a new myopathy on chromosome 8 of the mouse.

P. Lane, D. Myers, T. Beamer, 1976, The Journal of heredity.

The effect of restricted food intake on the life span of genetically obese mice.

M. Dickie, P. Lane, 1958, The Journal of nutrition.

Harlequin (Hw) produces progressive cerebellar cortical atrophy.

R. Bronson, M. Davisson, B. Harris, 1990 .

Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia, brachymorphic, and stubby.

M. Dickie, P. Lane, 1968, The Journal of heredity.

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.

L. Shultz, B. Wood, P. Lane, 1991, Laboratory investigation; a journal of technical methods and pathology.

WHIRLER MICE: A RECESSIVE BEHAVIOR MUTATION IN LINKAGE GROUP VIII.

P. Lane, 1963, The Journal of heredity.

Spasmodic, a mutation on chromosome 11 in the mouse.

W. White, P. Lane, A. Ganser, 1987, The Journal of heredity.

Osteopetrosis, a new recessive skeletal mutation on chromosome 12 of the mouse.

P. Lane, S. Marks,, Priscilla W. Lane, 1976, The Journal of heredity.

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

L. Donahue, R. Bronson, M. Davisson, 1998, The Journal of heredity.

The pituitary-gonad response of genetically obese mice in parabiosis with thin and obese siblings.

P. Lane, 1959, Endocrinology.

PHYSIOLOGICAL DIFFERENCES IN UTERI OF OBESE STOCK MICEA Comparison Between Obese Mice and their Thin Sibs

P. Lane, M. L. Drasher, M. Dicke, 1955 .

Fertile, obese male mice.

M. Dickie, P. Lane, 1954 .

New mutation causing sterility in the mouse.

M. Handel, M. Davisson, P. Lane, 1988, Gamete research.

Gene order in linkage group XVI of the house mouse.

P. Lane, E. Eicher, 1979, The Journal of heredity.

Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice.

M. Davisson, P. Lane, 1990, The Journal of heredity.

Adrenal tumors, pituitary tumors, and other pathological changes in F hybrids of strain DE x strain DBA.

M. Dickie, P. Lane, 1956, Cancer research.

Staggerer, a New Mutation in the Mouse Affecting the Cerebellum

R. Sidman, M. Dickie, P. Lane, 1962, Science.

Susceptibility to spontaneous pneumonitis in an inbred strain of beige and satin mice.

P. Lane, E. Murphy, 1972, Genetics.

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

L. Donahue, R. Bronson, K. Johnson, 2010, Blood.

Osteosclerosis, a recessive skeletal mutation on chromosome 19 in the mouse.

P. Lane, M. Seifert, S. Marks,, 1985, The Journal of heredity.

Ashen, a new color mutation on chromosome 9 of the mouse

J. Womack, P. Lane, 1979 .

MAHOGANY, A RECESSIVE COLOR MUTATION IN LINKAGE GROUP V OF THE MOUSE

P. Lane, Margaret C. Green, 1960 .

Assignment of LH XVI to chromosome 3 in the mouse.

P. Lane, E. Eicher, 1980, The Journal of heredity.

Two new mutations in linkage group XVI of the house mouse. Flaky tail and varitint-waddler-J.

P. Lane, 1972, The Journal of heredity.

Anorexia, a recessive mutation causing starvation in preweanling mice.

L. Maltais, W. Beamer, P. Lane, 1984, The Journal of heredity.

Pale ear and light ear in the house mouse. Mimic mutations in linkage groups XII and XVII.

E. L. Green, P. Lane, 1967, The Journal of heredity.

X-linked polydactyly (Xpl), a new mutation in the mouse.

P. Lane, H. Sweet, 1980, The Journal of heredity.

Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

P. Lane, C. Birkenmeier, 1993, Mammalian Genome.

Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse.

P. Lane, M. Deol, 1974, The Journal of heredity.

Chromosome 18 of the house mouse.

P. Lane, C. Beechey, E. Eicher, 1981, The Journal of heredity.

Crimpy (cpy) a new recessive hair mutation on chromosome 15 of the mouse

P. Lane, 1992 .

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

L. Donahue, R. Bronson, K. Johnson, 2010, Blood.

Linkage groups 3 and XVII in the mouse and the position of the light-ear locus.

P. Lane, 1967, The Journal of heredity.

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

R. Bronson, P. Lane, C. Spencer, 1992, The Journal of heredity.