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13 results for author:"Waymire K.G." in Literature citations

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The C57BL/6J Mouse Strain Background Modifies the Effect of a Mutation in Bcl2l2.

Navarro S.J., Trinh T., Lucas C.A., Ross A.J., Waymire K.G., Macgregor G.R.

G3 (Bethesda) 2:99-102(2012) · Mapped (12)

A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.

Fan W., Waymire K.G., Narula N., Li P., Rocher C., Coskun P.E., Vannan M.A., Narula J., Macgregor G.R., Wallace D.C.

Science 319:958-962(2008) · Mapped (9)

FNDC3A is required for adhesion between spermatids and Sertoli cells.

Obholz K.L., Akopyan A., Waymire K.G., MacGregor G.R.

Dev. Biol. 298:498-513(2006) · UniProtKB (3) · Mapped (4)

The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore.

Kokoszka J.E., Waymire K.G., Levy S.E., Sligh J.E., Cai J., Jones D.P., MacGregor G.R., Wallace D.C.

Nature 427:461-465(2004) · Mapped (5)

Mutation of a novel gene results in abnormal development of spermatid flagella, loss of intermale aggression and reduced body fat in mice.

Campbell P.K., Waymire K.G., Heier R.L., Sharer C., Day D.E., Reimann H., Jaje J.M., Friedrich G.A., Burmeister M., Bartness T.J. et al.

Genetics 162:307-320(2002) · UniProtKB (1) · Mapped (6)

Spermatogenesis in Bclw-deficient mice.

Russell L.D., Warren J., Debeljuk L., Richardson L.L., Mahar P.L., Waymire K.G., Amy S.P., Ross A.J., MacGregor G.R.

Biol. Reprod. 65:318-332(2001) · Mapped (3)

The combined functions of proapoptotic Bcl-2 family members bak and bax are essential for normal development of multiple tissues.

Lindsten T., Ross A.J., King A., Zong W.X., Rathmell J.C., Shiels H.A., Ulrich E., Waymire K.G., Mahar P., Frauwirth K. et al.

Mol. Cell 6:1389-1399(2000) · Mapped (10)

Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene.

Esposito L.A., Kokoszka J.E., Waymire K.G., Cottrell B., MacGregor G.R., Wallace D.C.

Free Radic. Biol. Med. 28:754-766(2000) · Mapped (2)

Increased affiliative response to vasopressin in mice expressing the V1a receptor from a monogamous vole.

Young L.J., Nilsen R., Waymire K.G., MacGregor G.R., Insel T.R.

Nature 400:766-768(1999) · UniProtKB (2) · Mapped (1)

Testicular degeneration in Bclw-deficient mice.

Ross A.J., Waymire K.G., Moss J.E., Parlow A.F., Skinner M.K., Russell L.D., Macgregor G.R.

Nat. Genet. 18:251-256(1998) · UniProtKB (1) · Mapped (2)

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.

Graham B.H., Waymire K.G., Cottrell B., Trounce I.A., MacGregor G.R., Wallace D.C.

Nat. Genet. 16:226-234(1997) · Mapped (5)

Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6.

Waymire K.G., Mahuren J.D., Jaje J.M., Guilarte T.R., Coburn S.P., MacGregor G.R.

Nat. Genet. 11:45-51(1995) · Mapped (8)

Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice.

Yokoyama T., Silversides D.W., Waymire K.G., Kwon B.S., Takeuchi T., Overbeek P.A.

Nucleic Acids Res. 18:7293-7298(1990) · Mapped (6)

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