Biological availability in animals of iron from common dietary sources von Fritz, James C, Pla, Gwendolyn W, Roberts, Talmadge, Boehne, J. William, Hove, Edwin L

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Effects of Pectin and Cellulose on Growth, Feed Efficiency, and Protein Utilization, and their Contribution to Energy Requirement and Cecal VFA in Rats von Hove, Edwin L., King, Susan

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The Ineffectiveness of Supplementary Cystine in Legume-Based Rat Diets von James, Kerry A.C., Hove, Edwin L.

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Composition and protein quality of sweet lupin seed von Hove, Edwin L.

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FDA's Altered Memo von Hove, Edwin L.

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The Effect of Formaldehyde on the Nutritive Value of Casein and Lactalbumin in the Diet of Rats von Hove, Edwin L., Lohrey, Evelyn

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Conditions affecting production of a protein isolate from lupin seed kernels von Ruiz Jr, Leonard P., Hove, Edwin L.

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The alkaloid content of sweet lupin seed used in feeding trials on pigs and rats von Ruiz, Leonard P., White, Sally F., Hove, Edwin L.

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Composition of sweet and bitter lupin seed hulls with observations on the apparent digestibility of sweet lupin seed hulls by young rats von Bailey, Raymond W., Mills, Susan E., Hove, Edwin L.

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Vitamins A and E in Deer Blood von Haugen, Arnold O., Hove, Edwin L.

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Anti-Vitamin E Stress Factors as Related to Lipid Peroxides von HOVE, EDWIN L.

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Photosensitivity from chlorophyll-derived pigments von Tapper, Brian A., Lohrey, Evelyn, Hove, Edwin L., Allison, Russell M.

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Note on the linoleic acid‐tocopherol relationship in fats and oils von Hove, Edwin L., Harris, Philip L.

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Ineffectiveness of Factor 3-Active Selenium Compounds in Muscular Dystrophy of Rabbits on Vitamin E-Free Diets von Hove, Edwin L., Fry, Gordon S., Schwarz, Klaus

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Thiamine Deficiency in Rabbits von Reid, Jeanne M., Hove, Edwin L., Braucher, Pela F., Mickelsen, Olaf

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ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis von Van Hove, Johan L.K., Friederich, Marisa W., Hock, Daniella H., Stroud, David A., Caruana, Nikeisha J., Christians, Uwe, Schniedewind, Björn, Michel, Cole R., Reisdorph, Richard, Lopez Gonzalez, Edwin D.J., Brenner, Charles, Donovan, Tonia E., Lee, Jessica C., Chatfield, Kathryn C., Larson, Austin A., Baker, Peter R., McCandless, Shawn E., Moore Burk, Meghan F.

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Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry von Chace, Donald H, Hillman, Steven L, Van Hove, Johan L. K, Naylor, Edwin W

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Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis von Frattini, Annalisa, Pangrazio, Alessandra, Susani, Lucia, Sobacchi, Cristina, Mirolo, Massimiliano, Abinun, Mario, Andolina, Marino, Flanagan, Adrienne, Horwitz, Edwin M, Mihci, Ercan, Notarangelo, Luigi D, Ramenghi, Ugo, Teti, Anna, Van Hove, Johan, Vujic, Dragana, Young, Terri, Albertini, Alberto, Orchard, Paul J, Vezzoni, Paolo, Villa, Anna

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Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder von Yoon, Wan Hee, Jangam, Sharayu, Davidson, Jean M., Grove, Megan E., Kohler, Jennefer N., Holmes, Matthew, Zhao, Chunli, Contrepois, Kévin, Heyman, Heino M., Webb-Robertson, Bobbie-Jo M., Alejandro, Mercedes E., Allard, Patrick, Balasubramanyam, Ashok, Barseghyan, Hayk, Bican, Anna, Birch, Camille L., Bostwick, Bret L., Briere, Lauren C., Brown, Donna M., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dayal, Jyoti G., Dell’Angelica, Esteban C., Dorset, Daniel C., Draper, David D., Eckstein, David J., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Ferreira, Carlos, Glanton, Emily, Godfrey, Rena A., Goldstein, David B., Gould, Sarah E., Gourdine, Jean-Philippe F., Hanchard, Neil A., Herzog, Matthew R., Hom, Jason, Howerton, Ellen M., Huang, Yong, Jacob, Howard J., Jiang, Yong-hui, Johnston, Jean M., Jones, Angela L., Kohane, Isaac S., Krier, Joel B., Lazar, Jozef, Lee, Hane, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, May, Thomas, McConkie-Rosell, Allyn, McCray, Alexa T., Moretti, Paolo M., Novacic, Donna, Orange, Jordan S., Palmer, Christina G.S., Potocki, Lorraine, Pusey, Barbara N., Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Samson, Susan L., Schoch, Kelly, Schroeder, Molly C., Shashi, Vandana, Silverman, Edwin K., Sinsheimer, Janet S., Spillmann, Rebecca C., Stong, Nicholas, Tifft, Cynthia J., Tran, Alyssa A., Valivullah, Zaheer M., Ward, Patricia A., Yamamoto, Shinya, Snyder, Michael, Merker, Jason D., Fisher, Paul G., Mayr, Johannes A., Morris, Andrew A., Schelley, Susan, Friederich, Marisa W., Yamamoto, Shinya, Wangler, Michael F., Taylor, Robert W., Bernstein, Jonathan A.

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The mutational spectrum of human malignant autosomal recessive osteopetrosis von SOBACCHI, Cristina, FRATTINI, Annalisa, DUPUIS-GIROD, Sophie, ELLIS, Ian, ETZIONI, Amos, FASTH, Anders, FISHER, Alain, GERRITSEN, Bert, GULINO, Virginia, HORWITZ, Edwin, KLAMROTH, Verena, LANINO, Edoardo, ORCHARD, Paul, MIROLO, Massimiliano, MUSIO, Antonio, MATTHIJS, Gert, NONOMAYA, Shigeaki, NOTARANGELO, Luigi D, OCHS, Hans D, SUPERTI FURGA, Andrea, VALIAHO, Jouni, VAN HOVE, Johan L. K, VIHINEN, Mauno, PORRAS, Oscar, VUJIC, Dragana, VEZZONI, Paolo, VILLA, Anna, TEZCAN, Ilhan, ANDOLINA, Marino, BABUL-HIRJI, Riyana, BARIC, Ivo, CANHAM, Natalie, CHITAYAT, David

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