Search Results - "Strickland, Laura"

Neuropilin-1 expression in cancer and development by Jubb, Adrian M, Strickland, Laura A, Liu, Scot D, Mak, Judy, Schmidt, Maike, Koeppen, Hartmut

“…Neuropilin (NRP)‐1 is a co‐receptor for vascular endothelial growth factor (VEGF). Preclinical data suggest that blockade of NRP1 suppresses tumour growth by…”
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The impact of Pompe disease on smooth muscle: a review by MCCALL, Angela L., SALEMI, Jeffrey, BHANAP, Preeti, STRICKLAND, Laura M., ELMALLAH, Mai K.

“…Pompe disease (OMIM 232300) is an autosomal recessive disorder caused by mutations in the gene encoding acid α-glucosidase (GAA) (EC 3.2.1.20), the enzyme…”
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Cancer-associated SMARCAL1 loss-of-function mutations promote alternative lengthening of telomeres and tumorigenesis in telomerase-negative glioblastoma cells by Liu, Heng, Xu, Cheng, Diplas, Bill H, Brown, Alexandrea, Strickland, Laura M, Yao, Haipei, Ling, Jinjie, McLendon, Roger E, Keir, Stephen T, Ashley, David M, He, Yiping, Waitkus, Matthew S

“…Abstract Background Telomere maintenance mechanisms are required to enable the replicative immortality of malignant cells. While most cancers activate the…”
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Glycogen accumulation in smooth muscle of a Pompe disease mouse model by McCall, Angela L., Dhindsa, Justin S., Bailey, Aidan M., Pucci, Logan A., Strickland, Laura M., ElMallah, Mai K.

“…Pompe disease is a lysosomal storage disease caused by mutations within the GAA gene, which encodes acid α-glucosidase (GAA)—an enzyme necessary for lysosomal…”
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Accumulation of pathological Ataxin‐7 in the medulla leads to hypoglossal (XII) motor unit pathology by Biswas, Debolina D., Strickland, Laura M., Dhindsa, Justin S., Shi, Yihan, Sethi, Ronit, Kehoe, Sean, Lai, Elias X., Huston, Meredith L., Scarrow, Evelyn R., ElMallah, Mai K.

“…SCA7 is an autosomal dominant neurological disorder caused by a deleterious CAG repeat expansion in the coding region of the ataxin‐7 gene on chromosome 3…”
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Motor axonopathies in a mouse model of Duchenne muscular dystrophy by Dhindsa, Justin S., McCall, Angela L., Strickland, Laura M., Fusco, Anna F., Kahn, Amanda F., ElMallah, Mai K.

“…Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease caused by deleterious mutations in the DMD gene which encodes the dystrophin protein…”
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What's new and what's next for gene therapy in Pompe disease? by Roger, Angela L, Sethi, Ronit, Huston, Meredith L, Scarrow, Evelyn, Bao-Dai, Joy, Lai, Elias, Biswas, Debolina D, El Haddad, Léa, Strickland, Laura M, Kishnani, Priya S, ElMallah, Mai K

“…Pompe disease is an autosomal recessive disorder caused by a deficiency of acid-α-glucosidase (GAA), an enzyme responsible for hydrolyzing lysosomal glycogen…”
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Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7 by Fusco, Anna F, Pucci, Logan A, Switonski, Pawel M, Biswas, Debolina D, McCall, Angela L, Kahn, Amanda F, Dhindsa, Justin S, Strickland, Laura M, La Spada, Albert R, ElMallah, Mai K

“…Spinocerebellar ataxia type 7 (SCA7) is an autosomal-dominant neurodegenerative disorder caused by a CAG repeat expansion in the coding region of the ataxin-7…”
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X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular disease by Gromova, Anastasia, Cha, Byeonggu, Robinson, Erica M, Strickland, Laura M, Nguyen, Nhat, ElMallah, Mai K, Cortes, Constanza J, La Spada, Albert R

“…X-linked spinal and bulbar muscular atrophy (SBMA; Kennedy's disease) is a rare neuromuscular disorder characterized by adult-onset proximal muscle weakness…”
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Plant macrofossil data for 48-0 ka in the USGS North American Packrat Midden Database, version 5.0 by Strickland, Laura E., Thompson, Robert S., Shafer, Sarah L., Bartlein, Patrick J., Pelltier, Richard T., Anderson, Katherine H., Schumann, R. Randall, McFadden, Andrew K.

“…Plant macrofossils from packrat ( Neotoma spp.) middens provide direct evidence of past vegetation changes in arid regions of North America. Here we describe…”
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Respiratory pathology in the Optn-/- mouse model of Amyotrophic Lateral Sclerosis by McCall, Angela L., Dhindsa, Justin S., Pucci, Logan A., Kahn, Amanda F., Fusco, Anna F., Biswas, Debolina D., Strickland, Laura M., Tseng, Henry C., ElMallah, Mai K.

“…•The optineurin-deficient mouse model (Optn-/-) exhibits respiratory insufficiency during a hypoxic and hypercapnic challenge.•Motor neuron loss is evident in…”
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Neotectonic Mapping of Puerto Rico by Thompson Jobe, Jessie, Briggs, Richard, Hughes, Kenneth Stephen, Joyce, James, Gold, Ryan, Mahan, Shannon, Gray, Harrison, Strickland, Laura

“…Puerto Rico is part of the Puerto Rico-Virgin Islands microplate, along the Caribbean–North American plate boundary between the Puerto Rico trench subduction…”
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Corrigendum to “Respiratory pathology in the optn-/- mouse model of amyotrophic lateral sclerosis” [Respir. Physiol. Neurobiol. 282 (2020) 103525] by McCall, Angela L., Dhindsa, Justin S., Pucci, Logan A., Khan, Amanda F., Fusco, Anna F., Biswas, Debolina D., Strickland, Laura M., Tseng, Henry C., ElMallah, Mai K.

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Respiratory neuropathology in spinocerebellar ataxia type 7 by Biswas, Debolina D, Shi, Yihan, El Haddad, Léa, Sethi, Ronit, Huston, Meredith, Kehoe, Sean, Scarrow, Evelyn R, Strickland, Laura M, Pucci, Logan A, Dhindsa, Justin S, Hunanyan, Ani, La Spada, Albert R, ElMallah, Mai K

“…Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant neurological disorder caused by deleterious CAG repeat expansion in the coding region of the…”
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Preclinical evaluation of carcinoembryonic cell adhesion molecule (CEACAM) 6 as potential therapy target for pancreatic adenocarcinoma by Strickland, Laura A, Ross, Jed, Williams, Simon, Ross, Sarajane, Romero, Maria, Spencer, Susan, Erickson, Rich, Sutcliffe, Julie, Verbeke, Caroline, Polakis, Paul, van Bruggen, Nicholas, Koeppen, Hartmut

“…Despite the availability of new targeted therapies, ductal pancreatic adenocarcinoma continues to carry a poor prognosis. Carcinoembryonic antigen-related cell…”
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Neuropilin-2 expression in cancer by Jubb, Adrian M, Sa, Susan M, Ratti, Navneet, Strickland, Laura A, Schmidt, Maike, Callahan, Christopher A, Koeppen, Hartmut

“…Jubb A M, Sa S M, Ratti N, Strickland L A, Schmidt M, Callahan C A & Koeppen H 
(2012) Histopathology 61, 340–349 Neuropilin‐2 expression in cancer Aims: …”
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Plasmalemmal vesicle-associated protein (PLVAP) is expressed by tumour endothelium and is upregulated by vascular endothelial growth factor-A (VEGF) by Strickland, Laura A, Jubb, Adrian M, Hongo, Jo-Anne, Zhong, Fiona, Burwick, Jennifer, Fu, Ling, Frantz, Gretchen D, Koeppen, Hartmut

“…Vascular endothelial growth factor‐A (VEGF) is an important regulator of vascular permeability. In preclinical studies, VEGF induces endothelial fenestrations…”
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Comments on plasmalemmal vesicle associated protein-1 as a novel marker implicated in brain tumor angiogenesis by Sanders Strickland, Laura A, Koeppen, Hartmut

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The Danielson Evaluation System in Two Mid-South High Schools: A Case Study by Strickland, Laura Bailey

“…The purpose of this study is to answer the question: How do pilot users of the Danielson Evaluation System perceive this model in two mid-south high schools?…”
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Phrenic and Hypoglossal motor unit pathology in a Spinocerebellar ataxia type 7 mouse model by Biswas, Debolina, Dhindsa, Justin, Strickland, Laura, Pucci, Logan, ElMallah, Mai

“…Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant neurodegenerative disorder caused by a deleterious CAG repeat expansion in the coding region of…”
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