Search Results - "Boissy, Y L"

Water Disrupts Stratum Corneum Lipid Lamellae: Damage is Similar to Surfactants by WARNER, R. R, BOISSY, Y. L, LILLY, N. A, SPEARS, M. J, MCKILLOP, K, MARSHALL, J. L, STONE, K. J

“…Using electron microscopy, we investigated the effect of (i) a dilute surfactant and of water alone on the ultrastructure of stratum corneum lipids in pig skin…”
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Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism : A new subtype of albinism classified as OCA3 by BOISSY, R. E, ZHAO, H, NORDLUND, J. J, OETTING, W. S, AUSTIN, L. M, WILDENBERG, S. C, BOISSY, Y. L, ZHAO, Y, STURM, R. A, HEARING, V. J, KING, R. A

“…Most types of human oculocutaneous albinism (OCA) result from mutations in the gene for tyrosinase (OCA1) or the P protein (OCA2), although other types of OCA…”
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On the analysis of the pathophysiology of Chediak-Higashi syndrome. Defects expressed by cultured melanocytes by Zhao, H, Boissy, Y L, Abdel-Malek, Z, King, R A, Nordlund, J J, Boissy, R E

“…The Chediak-Higashi syndrome (CHS) is a disorder that affects the synthesis and/or maintenance of storage/secretory granules in various types of cells…”
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Misrouting of tyrosinase with a truncated cytoplasmic tail as a result of the murine platinum ( c p) mutation by Beermann, Friedrich, Orlow, Seth J., Boissy, Raymond E., Schmidt, Andrea, Boissy, Ying L., Lamoreux, M. Lynn

“…Mice homozygous for the platinum ( c p) allele at the albino locus manifest severe oculocutaneous albinism despite the presence in vitro of tyrosinase activity…”
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Characterization of Vernix Caseosa: Water Content, Morphology, and Elemental Analysis by Pickens, William L., Warner, Ronald R., Boissy, Ying L., Boissy, Raymond E., Hoath, Steven B.

“…Recent studies have prompted interest in the use of epidermal barrier creams as protective biofilms for very low birthweight preterm infants. The key to…”
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Ocular pathology in mice with a transgenic insertion at the microphthalmia locus by Boissy, R E, Boissy, Y L, Krakowsky, J M, Lamoreux, M L, Lingrel, J B, Nordlund, J J

“…A DNA insertional mutation at the microphthalmia locus (mi) in a transgenic mouse has been developed and given the allele symbol of mitg (Krakowsky et al.,…”
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Chronic Growth Stimulation of Human Adult Melanocytes by Inflammatory Mediators in vitro: Implications for Nevus Formation and Initial Steps in Melanocyte Oncogenesis by Medrano, Estela E., Farooqui, Jamal Z., Boissy, Raymond E., Boissy, Ying Liu, Akadiri, Bola, Nordlund, James J.

“…In the human epidermis, melanocytes are distributed at a distance from each other. In contrast, melanocytes in nevi, which are considered benign neoplasms of…”
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Neurofibromin-deficient fibroblasts fail to form perineurium in vitro by Rosenbaum, T, Boissy, Y L, Kombrinck, K, Brannan, C I, Jenkins, N A, Copeland, N G, Ratner, N

“…To identify cell type(s) that might contribute to nerve sheath tumors (neurofibromas) in patients with neurofibromatosis type 1, we generated cell cultures…”
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Hydration Disrupts Human Stratum Corneum Ultrastructure by Warner, Ronald R., Stone, Keith J., Boissy, Ying L.

“…Using transmission and cryo-scanning electron microscopy, we confirm that extended water exposure leads to extensive disruption of stratum corneum…”
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Neurofibromin, the Neurofibromatosis Type 1 Ras-GAP, Is Required for Appropriate P0 Expression and Myelination by ROSENBAUM, THORSTEN, KIM, HAESUN A., BOISSY, YING L., LING, BO, RATNER, NANCY

“…The neurofibromatosis type 1 (NF1) gene product, neurofibromin, regulates activation of the Ras intracellular signaling pathway in Schwann cells. Schwann cells…”
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Mutation in and lack of expression of tyrosine-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: A new subtype of albinism classified as "OCA3" by Boissy, R E, Zhao, H, Oetting, W S, Austin, L M, Wildenberg, S C, Boissy, Y L, Zhao, Y, Sturm, R A, Hearing, V J

“…Most types of human oculocutaneous albinism (OCA) result from mutations in the gene for tyrosinase (OCA1) or the P protein (OCA2), although other types of OCA…”
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Smyth chicken melanocyte autoantibodies: cross-species recognition, in vivo binding, and plasma membrane reactivity of the antiserum by Searle, E A, Austin, L M, Boissy, Y L, Zhao, H, Nordlund, J J, Boissy, R E

“…Smyth line (SL) chickens, which develop a depigmenting disorder similar to human vitiligo, produce circulating anti-melanocyte antibodies (Austin, L.M. et al.,…”
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