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GM05659 Fibroblast from Skin, Chest

Description:

APPARENTLY HEALTHY INDIVIDUAL

Affected:

No

Sex:

Male

Age:

1 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Images
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Apparently Healthy Collection
Biopsy Source Chest
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Sample Source Fibroblast from Skin, Chest
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Skin biopsy (chest); 46,XY

Characterizations

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PDL at Freeze 4.41
Passage Frozen 4
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis
 

Phenotypic Data

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Remarks Skin biopsy (chest); 46,XY

Publications

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Sanchez KL, Kim J, White JB, Tolan A, Rajagopal NP, Anderson DW, Shin AN, Shin SD, Currais A, Soriano-Castell D, Maher P, Soriano S, Evidence of Oxytosis/Ferroptosis in Niemann-Pick Disease Type C International journal of molecular sciences26: 2025
PubMed ID: 40243519
 
Hamamoto A, Kita N, Gowda SGB, Takatsu H, Nakayama K, Arita M, Hui SP, Shin HW, Lysosomal membrane integrity in fibroblasts derived from patients with Gaucher disease Cell structure and function26: 2024
PubMed ID: 38072450
 
Nunes MJ, Carvalho AN, Reis J, Costa D, Moutinho M, Mateus J, de Almeida RM, Brito S, Risso D, Nunes S, Castro-Caldas M, Gama MJ, Rodrigues CMP, Xapelli S, Diógenes MJ, Cartier N, Chali F, Piguet F, Rodrigues E, Cholesterol redistribution triggered by CYP46A1 gene therapy improves major hallmarks of Niemann-Pick type C disease but is not sufficient to halt neurodegeneration Biochimica et biophysica acta Molecular basis of disease26:166993 2024
PubMed ID: 38142760
 
Ullman JC, Dick RA, Linzner D, Minga T, Tep S, Satterfield TF, Xi Y, Beattie DT, Marmon T, Neutel JM, Chung B, Leeds JM, Noonberg SB, Green EM, Bernstein HS, First-in-Human Evaluation of Safety, Pharmacokinetics and Muscle Glycogen Lowering of a Novel Glycogen Synthase 1 Inhibitor for the Treatment of Pompe Disease Clinical pharmacology and therapeutics116:1580-1592 2024
PubMed ID: 39439155
 
Han S, Wang Q, Song Y, Pang M, Ren C, Wang J, Guan D, Xu W, Li F, Wang F, Zhou X, Fernández-Hernando C, Zhang H, Wu D, Ye Z, Lithium ameliorates Niemann-Pick C1 disease phenotypes by impeding STING/SREBP2 activation iScience26:106613 2023
PubMed ID: 37128603
 
Lieberman R, Cortes LK, Gao G, Park H, Wang B, Jones PL, Hunter RB, Leonard JP, Barker RH, Human iPSC-derived astrocytes generated from donors with globoid cell leukodystrophy display phenotypes associated with disease PloS one17:e0271360 2022
PubMed ID: 35921286
 
Panagaki T, Pecze L, Randi EB, Nieminen AI, Szabo C, Role of the cystathionine ß-synthase / H Redox biology55:102416 2022
PubMed ID: 35921774
 
Argüello G, Balboa E, Tapia PJ, Castro J, Yañez MJ, Mattar P, Pulgar R, Zanlungo S, Genistein Activates Transcription Factor EB and Corrects Niemann-Pick C Phenotype International journal of molecular sciences22:102416 2021
PubMed ID: 33921734
 
Huang X, Roeder A, Li R, Beers J, Liu C, Zou J, Yu PB, Zheng W, Generation of an induced pluripotent stem cell line (TRNDi012-B) from Fibrodysplasia Ossificans Progressiva (FOP) patient carrying a heterozygous mutation c 617G > A in the ACVR1 gene Stem cell research54:102424 2021
PubMed ID: 34139597
 
Kang I, Yoo JM, Kim D, Kim J, Cho MK, Lee SE, Kim DJ, Lee BC, Lee JY, Kim JJ, Shin N, Choi SW, Lee YH, Ko HS, Shin S, Hong BH, Kang KS, Graphene Quantum Dots Alleviate Impaired Functions in Niemann-Pick Disease Type C in Vivo Nano letters21:2339-2346 2021
PubMed ID: 33472003
 
Kutchukian C, Vivas O, Casas M, Jones JG, Tiscione SA, Simó S, Ory DS, Dixon RE, Dickson EJ, NPC1 regulates the distribution of phosphatidylinositol 4-kinases at Golgi and lysosomal membranes The EMBO journal21:e105990 2021
PubMed ID: 34019311
 
Ohashi M, Tamura A, Yui N, Terminal Structure of Triethylene Glycol-Tethered Chains on ß-Cyclodextrin-Threaded Polyrotaxanes Dominates Temperature Responsivity and Biointeractions Langmuir : the ACS journal of surfaces and colloids37:11102-11114 2021
PubMed ID: 34478294
 
Pradhan M, Farkhondeh A, Cheng YS, Xu M, Beers J, Zou J, Liu C, Might M, Rodems S, Baumgärtel K, Zheng W, An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, pR390P and pL318P, in the NGLY1 gene Stem cell research54:102400 2021
PubMed ID: 34051448
 
Botté A, Lainé J, Xicota L, Heiligenstein X, Fontaine G, Kasri A, Rivals I, Goh P, Faklaris O, Cossec JC, Morel E, Rebillat AS, Nizetic D, Raposo G, Potier MC, Ultrastructural and dynamic studies of the endosomal compartment in Down syndrome Acta neuropathologica communications8:89 2020
PubMed ID: 32580751
 
Du W, Gu M, Hu M, Pinchi P, Chen W, Ryan M, Nold T, Bannaga A, Xu H, Lysosomal Zn Cell reports37:109848 2020
PubMed ID: 34686351
 
Even A, Morelli G, Turchetto S, Shilian M, Bail RL, Laguesse S, Krusy N, Brisker A, Brandis A, Inbar S, Chariot A, Saudou F, Dietrich P, Dragatsis I, Brone B, Broix L, Rigo JM, Weil M, Nguyen L, ATP-citrate lyase promotes axonal transport across species Nature communications12:5878 2020
PubMed ID: 34620845
 
Goedeke L, Canfrán-Duque A, Rotllan N, Chaube B, Thompson BM, Lee RG, Cline GW, McDonald JG, Shulman GI, Lasunción MA, Suárez Y, Fernández-Hernando C, MMAB promotes negative feedback control of cholesterol homeostasis Nature communications12:6448 2020
PubMed ID: 34750386
 
Ilnytska O, Lai K, Gorshkov K, Schultz ML, Tran BN, Jeziorek M, Kunkel TJ, Azaria RD, McLoughlin HS, Waghalter M, Xu Y, Schlame M, Altan-Bonnet N, Zheng W, Lieberman AP, Dobrowolski R, Storch J, Enrichment of NPC1-deficient cells with the lipid LBPA stimulates autophagy, improves lysosomal function, and reduces cholesterol storage The Journal of biological chemistry12:100813 2020
PubMed ID: 34023384
 
Janes V, Grabany S, Delbrouck J, Vincent SP, Gottschalk J, Elling L, Hanisch FG, Fluorinated Galactoses Inhibit Galactose-1-Phosphate Uridyltransferase and Metabolically Induce Galactosemia-like Phenotypes in HEK-293 Cells Cells9:100813 2020
PubMed ID: 32138379
 
Lee SE, Shin N, Kook MG, Kong D, Kim NG, Choi SW, Kang KS, Human iNSC-derived brain organoid model of lysosomal storage disorder in Niemann-Pick disease type C Cell death & disease11:1059 2020
PubMed ID: 33311479
 
Li R, Pradhan M, Xu M, Roeder A, Beers J, Zou J, Liu C, Porter FD, Zheng W, An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p I1061T (c 3182T>C) mutation in the NPC1 gene Stem cell research44:101737 2020
PubMed ID: 32114296
 
Mullegama SV, Klein SD, Williams SR, Innis JW, Probst FJ, Haldeman-Englert C, Martinez-Agosto JA, Yang Y, Tian Y, Elsea SH, Ezashi T, Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes Scientific reports11:11295 2020
PubMed ID: 34050248
 
Panagaki T, Randi EB, Szabo C, Role of 3-Mercaptopyruvate Sulfurtransferase in the Regulation of Proliferation and Cellular Bioenergetics in Human Down Syndrome Fibroblasts Biomolecules10:11295 2020
PubMed ID: 32340322
 
Subramanian K, Hutt DM, Scott SM, Gupta V, Mao S, Balch WE, Correction of Niemann-Pick type C1 trafficking and activity with the histone deacetylase inhibitor valproic acid The Journal of biological chemistry10:11295 2020
PubMed ID: 32354745
 
Yañez MJ, Campos F, Marín T, Klein AD, Futerman AH, Alvarez AR, Zanlungo S, c-Abl activates RIPK3 signaling in Gaucher disease Biochimica et biophysica acta Molecular basis of disease1867:166089 2020
PubMed ID: 33549745
 
Yañez MJ, Marín T, Balboa E, Klein AD, Alvarez AR, Zanlungo S, Finding pathogenic commonalities between Niemann-Pick type C and other lysosomal storage disorders: Opportunities for shared therapeutic interventions Biochimica et biophysica acta Molecular basis of disease1866:165875 2020
PubMed ID: 32522631
 
Baskfield A, Li R, Beers J, Zou J, Liu C, Zheng W, Generation of an induced pluripotent stem cell line (TRNDi004-I) from a Niemann-Pick disease type B patient carrying a heterozygous mutation of pL43_A44delLA in the SMPD1 gene Stem cell research37:101436 2019
PubMed ID: 31009819
 
Baskfield A, Li R, Beers J, Zou J, Liu C, Zheng W, An induced pluripotent stem cell line (TRNDi009-C) from a Niemann-Pick disease type A patient carrying a heterozygous pL302P (c905 T>C) mutation in the SMPD1 gene Stem cell research38:101461 2019
PubMed ID: 31132580
 
Cheng YS, Li R, Baskfield A, Beers J, Zou J, Liu C, Zheng W, A human induced pluripotent stem cell line (TRNDi007-B) from an infantile onset Pompe patient carrying pR854X mutation in the GAA gene Stem cell research37:101435 2019
PubMed ID: 31026687
 
Colussi DJ, Jacobson MA, Patient-Derived Phenotypic High-Throughput Assay to Identify Small Molecules Restoring Lysosomal Function in Tay-Sachs Disease SLAS discovery : advancing life sciences R & D24:295-303 2019
PubMed ID: 30616450
 
Huang W, Xu M, Li R, Baskfield A, Kouznetsova J, Beers J, Zou J, Liu C, Zheng W, An induced pluripotent stem cell line (TRNDi006-A) from a MPS IIIB patient carrying homozygous mutation of pGlu153Lys in the NAGLU gene Stem cell research37:101427 2019
PubMed ID: 30933722
 
Hwang S, Williams JF, Kneissig M, Lioudyno M, Rivera I, Helguera P, Busciglio J, Storchova Z, King MC, Torres EM, Suppressing Aneuploidy-Associated Phenotypes Improves the Fitness of Trisomy 21 Cells Cell reports29:2473-2488.e5 2019
PubMed ID: 31747614
 
Kassam S, Understanding Experiences of Social Support as Coping Resources among Immigrant and Refugee Women with Postpartum Depression: An Integrative Literature Review Issues in mental health nursing29:1-13 2019
PubMed ID: 31070499
 
Lawrence R, Prill H, Vachali PP, Adintori EG, de Hart G, Wang RY, Burton BK, Pasquali M, Crawford BE, Characterization of disease-specific chondroitin sulfate non-reducing end accumulation in mucopolysaccharidosis IVA Glycobiology29:1-13 2019
PubMed ID: 31897472
 
Li R, Baskfield A, Beers J, Zou J, Liu C, Alméciga-Díaz CJ, Zheng W, Generation of an induced pluripotent stem cell line (TRNDi005-A) from a Mucopolysaccharidosis Type IVA (MPS IVA) patient carrying compound heterozygous pR61W and pWT405del mutations in the GALNS gene Stem cell research36:101408 2019
PubMed ID: 30797135
 
Singhal A, Krystofiak ES, Jerome WG, Song B, 2-Hydroxypropyl-gamma-cyclodextrin overcomes NPC1 deficiency by enhancing lysosome-ER association and autophagy Scientific reports10:8663 2019
PubMed ID: 32457374
 
Tiscione SA, Vivas O, Ginsburg KS, Bers DM, Ory DS, Santana LF, Dixon RE, Dickson EJ, Disease-associated mutations in Niemann-Pick type C1 alter ER calcium signaling and neuronal plasticity The Journal of cell biology10:8663 2019
PubMed ID: 31601621
 
Xu X, Pradhan M, Xu M, Cheng YS, Beers J, Linask KL, Lin Y, Zheng W, Zou J, Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D, TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy individuals Stem cell research49:102011 2019
PubMed ID: 33038742
 
Yang S, Cheng YS, Li R, Pradhan M, Hong J, Beers J, Zou J, Liu C, Might M, Rodems S, Zheng W, An induced pluripotent stem cell line (TRNDi010-C) from a patient carrying a homozygous pR401X mutation in the NGLY1 gene Stem cell research39:101496 2019
PubMed ID: 31326749
 
Ahmed AA1, Smoczer C1, Pace B1, Patterson D2,3, Cress Cabelof D1., Loss of DNA polymerase β induces cellular senescence Environmental and Molecular Mutagenesis 39:101496 2018
PubMed ID: 29968395
 
Ashutosh Singhal, Lajos Szente, James E. K. Hildreth & Byeongwoon Song, Hydroxypropyl-beta and -gamma cyclodextrins rescue cholesterol accumulation in Niemann–Pick C1 mutant cell via lysosome-associated membrane protein 1 Cell Death and Disease9:1019 2018
PubMed ID: 30282967
 
Fleischer JG, Schulte R, Tsai HH, Tyagi S, Ibarra A, Shokhirev MN, Huang L, Hetzer MW, Navlakha S, Predicting age from the transcriptome of human dermal fibroblasts Genome Biology19:1019 2018
PubMed ID: 30567591
 
Flint M, Chatterjee P, Lin DL, McMullan LK, Shrivastava-Ranjan P, Bergeron É, Lo MK, Welch SR, Nichol ST, Tai AW, Spiropoulou CF, A genome-wide CRISPR screen identifies N-acetylglucosamine-1-phosphate transferase as a potential antiviral target for Ebola virus Nature communications10:285 2018
PubMed ID: 30655525
 
Fog CK, Zago P, Malini E, Solanko LM, Peruzzo P, Bornaes C, Magnoni R, Mehmedbasic A, Petersen NHT, Bembi B, Aerts JFMG, Dardis A, Kirkegaard T, The heat shock protein amplifier arimoclomol improves refolding, maturation and lysosomal activity of glucocerebrosidase EBioMedicine38:142-153 2018
PubMed ID: 30497978
 
Kim Y1, Zheng X2, Ansari Z1, Bunnell MC1, Herdy JR1, Traxler L3, Lee H1, Paquola ACM4, Blithikioti C1, Ku M5, Schlachetzki JCM6, Winkler J7, Edenhofer F8, Glass CK9, Paucar AA1, Jaeger BN1, Pham S1, Boyer L1, Campbell BC1, Hunter T2, Mertens J10, Gage FH, Mitochondrial Aging Defects Emerge in Directly Reprogrammed Human Neurons due to Their Metabolic Profile Cell Reports23:2550-2558 2018
PubMed ID: 29847787
 
Li R, Baskfield A, Lin Y, Beers J, Zou J, Liu C, Jaffré F, Roberts AE, Ottinger EA, Kontaridis MI, Zheng W, Generation of an induced pluripotent stem cell line (TRNDi003-A) from a Noonan syndrome with multiple lentigines (NSML) patient carrying a pQ510P mutation in the PTPN11 gene Stem cell research34:101374 2018
PubMed ID: 30640061
 
Mylinh Vu, Rong Li, Amanda Baskfield, Billy Lu, Atena Farkhondeh, Kirill Gorshkov, Omid Motabar, Jeanette Beers, Guokai Chen, Jizhong Zou, Angela J. Espejo-Mojica, Alexander Rodríguez-López, Carlos J. Alméciga-Díaz, Luis A. Barrera, Xuntian Jiang, Daniel S. Ory, Juan J. Marugan and Wei Zheng, Neural stem cells for disease modeling and evaluation of therapeutics for Tay-Sachs disease Orphanet Journal of Rare Diseases13:152 2018
PubMed ID: 30220252
 
Vivas O, Tiscione SA, Dixon RE, Ory DS, Dickson EJ, Niemann-Pick Type C Disease Reveals a Link between Lysosomal Cholesterol and PtdIns(4,5)P Cell reports27:2636-2648.e4 2018
PubMed ID: 31141688
 
Wang C, Scott SM, Subramanian K, Loguercio S, Zhao P, Hutt DM, Farhat NY, Porter FD, Balch WE, Quantitating the epigenetic transformation contributing to cholesterol homeostasis using Gaussian process Nature communications10:5052 2018
PubMed ID: 31699992
 
György B, Cruz L, Yellen D, Aufiero M, Alland I, Zhang X, Ericsson M, Fraefel C, Li YC, Takeda S, Hyman BT, Breakefield XO, Mutant torsinA in the heterozygous DYT1 state compromises HSV propagation in infected neurons and fibroblasts Scientific reports8:2324 2017
PubMed ID: 29396398
 
Sima N, Li R, Huang W, Xu M, Beers J, Zou J, Titus S, Ottinger EA, Marugan JJ, Xie X, Zheng W, Neural stem cells for disease modeling and evaluation of therapeutics for infantile (CLN1/PPT1) and late infantile (CLN2/TPP1) neuronal ceroid lipofuscinoses Orphanet journal of rare diseases13:54 2017
PubMed ID: 29631617
 
Corcelle-Termeau E, Vindeløv SD, Hämälistö S, Mograbi B, Keldsbo A, Bräsen JH, Favaro E, Adam D, Szyniarowski P, Hofman P, Krautwald S, Farkas T, Petersen NH, Rohde M, Linkermann A, Jäättelä M, Excess sphingomyelin disturbs ATG9A trafficking and autophagosome closure Autophagy12:833-49 2016
PubMed ID: 27070082
 
Salman A, Cougnoux A, Farhat N, Wassif CA, Porter FD, Association of NPC1 variant pP237S with a pathogenic splice variant in two Niemann-Pick disease type C1 patients American journal of medical genetics Part A173:1038-1040 2016
PubMed ID: 28328115
 
Long Y, Xu M, Li R, Dai S, Beers J, Chen G, Soheilian F, Baxa U, Wang M, Marugan JJ, Muro S, Li Z, Brady R, Zheng W, Induced Pluripotent Stem Cells for Disease Modeling and Evaluation of Therapeutics for Niemann-Pick Disease Type A Stem cells translational medicine5:1644-1655 2015
PubMed ID: 27484861
 
Xu CC, Denton KR, Wang ZB, Zhang X, Li XJ, Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophy Disease models & mechanisms9:39-49 2015
PubMed ID: 26586529
 
Yu D, Swaroop M, Wang M, Baxa U, Yang R, Yan Y, Coksaygan T, DeTolla L, Marugan JJ, Austin CP, McKew JC, Gong DW, Zheng W, Niemann-Pick Disease Type C: Induced Pluripotent Stem Cell-Derived Neuronal Cells for Modeling Neural Disease and Evaluating Drug Efficacy Journal of biomolecular screening19:1164-73 2014
PubMed ID: 24907126
 
Chen JY, Lin JR, Tsai FC, Meyer T., Dosage of Dyrk1a Shifts Cells within a p21-Cyclin D1 Signaling Map to Control the Decision to Enter the Cell Cycle. Mol Cell.52(1):87-100 2013
PubMed ID: 24119401
 
Singh RD, Schroeder AS, Scheffer L, Holicky EL, Wheatley CL, Marks DL, Pagano RE, Prominin-2 expression increases protrusions, decreases caveolae and inhibits Cdc42 dependent fluid phase endocytosis Biochemical and biophysical research communications434:466-72 2013
PubMed ID: 23583380
 
Xu M, Liu K, Swaroop M, Sun W, Dehdashti SJ, McKew JC, Zheng W, A phenotypic compound screening assay for lysosomal storage diseases Journal of biomolecular screening19:168-75 2013
PubMed ID: 23983233
 
Appelqvist H, Sandin L, Björnström K, Saftig P, Garner B, Ollinger K, Kågedal K, Sensitivity to lysosome-dependent cell death is directly regulated by lysosomal cholesterol content PloS one7:e50262 2012
PubMed ID: 23166840
 
Swaroop M1, Thorne N, Rao MS, Austin CP, McKew JC, Zheng W., Evaluation of cholesterol reduction activity of methyl-β-cyclodextrin using differentiated human neurons and astrocytes. J Biomol Screen17(9):1243-51 2012
PubMed ID: 22923786
 
Thacker JD1, Balin BJ, Appelt DM, Sassi-Gaha S, Purohit M, Rest RF, Artlett CM., NLRP3 inflammasome is a target for development of broad-spectrum anti-infective drugs. Antimicrob Agents Chemother56(4):1921-30 2012
PubMed ID: 22290938
 
Xu M1, Liu K, Swaroop M, Porter FD, Sidhu R, Firnkes S, Ory DS, Marugan JJ, Xiao J, Southall N, Pavan WJ, Davidson C, Walkley SU, Remaley AT, Baxa U, Sun W, McKew JC, Austin CP, Zheng W., δ-Tocopherol reduces lipid accumulation in Niemann-Pick type C1 and Wolman cholesterol storage disorders. J Biol Chem287(47):39349-60 2012
PubMed ID: 23035117
 
Brett CL, Kallay L, Hua Z, Green R, Chyou A, Zhang Y, Graham TR, Donowitz M, Rao R, Genome-wide analysis reveals the vacuolar pH-stat of Saccharomyces cerevisiae PloS one6:e17619 2011
PubMed ID: 21423800
 
Arora S, Gonzales IM, Hagelstrom RT, Beaudry C, Choudhary A, Sima C, Tibes R, Mousses S, Azorsa DO, RNAi phenotype profiling of kinases identifies potential therapeutic targets in Ewing's sarcoma Molecular cancer9:218 2010
PubMed ID: 20718987
 
Sassi-Gaha S, Loughlin DT, Kappler F, Schwartz ML, Su B, Tobia AM, Artlett CM, Two dicarbonyl compounds, 3-deoxyglucosone and methylglyoxal, differentially modulate dermal fibroblasts Matrix biology : journal of the International Society for Matrix Biology29:127-34 2009
PubMed ID: 19800404
 
Duarte TL, Cooke MS, Jones GD, Gene expression profiling reveals new protective roles for vitamin C in human skin cells Free radical biology & medicine46:78-87 2008
PubMed ID: 18973801
 
Goel A, Carlson SK, Classic KL, Greiner S, Power AT, Bell JC, Russell SJ, Radioiodide imaging and radiovirotherapy of multiple myeloma using VSV({Delta}51)-NIS, an attenuated vesicular stomatitis virus encoding the sodium iodide symporter gene Blood110(7):2342-49 2007
PubMed ID: 17515401
 
Ladasky JJ, Boyle S, Seth M, Li H, Pentcheva T, Abe F, Steinberg SJ, Edidin M, Bap31 enhances the endoplasmic reticulum export and quality control of human class I MHC molecules Journal of immunology (Baltimore, Md : 1950)177:6172-81 2006
PubMed ID: 17056546
 
Singh RD, Liu Y, Wheatley CL, Holicky EL, Makino A, Marks DL, Kobayashi T, Subramaniam G, Bittman R, Pagano RE, Caveolar endocytosis and microdomain association of a glycosphingolipid analog is dependent on its sphingosine stereochemistry The Journal of biological chemistry281:30660-8 2006
PubMed ID: 16893900
 
Choudhury A, Marks DL, Proctor KM, Gould GW, Pagano RE, Regulation of caveolar endocytosis by syntaxin 6-dependent delivery of membrane components to the cell surface Nature cell biology8:317-28 2005
PubMed ID: 16565709
 
Narita K, Choudhury A, Dobrenis K, Sharma DK, Holicky EL, Marks DL, Walkley SU, Pagano RE, Protein transduction of Rab9 in Niemann-Pick C cells reduces cholesterol storage The FASEB journal : official publication of the Federation of American Societies for Experimental Biology19:1558-60 2005
PubMed ID: 15972801
 
Passeggio J, Liscum L, Flux of fatty acids through NPC1 lysosomes The Journal of biological chemistry280:10333-9 2005
PubMed ID: 15632139
 
Pipalia NH, Huang A, Ralph H, Rujoi M, Maxfield FR, Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells Journal of lipid research47:284-301 2005
PubMed ID: 16288097
 
Sharma DK, Brown JC, Cheng Z, Holicky EL, Marks DL, Pagano RE, The glycosphingolipid, lactosylceramide, regulates beta1-integrin clustering and endocytosis. Cancer Res65(18):8233-41 2005
PubMed ID: 16166299
 
Walker LC, Overstreet MA, Siddiqui A, De Paepe A, Ceylaner G, Malfait F, Symoens S, Atsawasuwan P, Yamauchi M, Ceylaner S, Bank RA, Yeowell HN, A novel mutation in the lysyl hydroxylase 1 gene causes decreased lysyl hydroxylase activity in an Ehlers-Danlos VIA patient The Journal of investigative dermatology124:914-8 2005
PubMed ID: 15854030
 
Choudhury A, Sharma DK, Marks DL, Pagano RE, ted Endosomal Cholesterol in Niemann-Pick Cells Inhibits Rab4 and Perturbs Membrane Recycling. Mol Biol CellEpub ahead of print:914-8 2004
PubMed ID: 15292453
 
Sharma DK, Brown JC, Choudhury A, Peterson TE, Holicky E, Marks DL, Simari R, Parton RG, Pagano RE, Selective stimulation of caveolar endocytosis by glycosphingolipids and cholesterol. Mol Biol Cell15(7):3114-22 2004
PubMed ID: 15107466
 
Greco M, Villani G, Mazzucchelli F, Bresolin N, Papa S, Attardi G, Marked aging-related decline in efficiency of oxidative phosphorylation in human skin fibroblasts The FASEB journal : official publication of the Federation of American Societies for Experimental Biology17:1706-8 2003
PubMed ID: 12958183
 
Kwik J, Boyle S, Fooksman D, Margolis L, Sheetz MP, Edidin M, Membrane cholesterol, lateral mobility, and the phosphatidylinositol 4,5-bisphosphate-dependent organization of cell actin. Proc Natl Acad Sci U S A100(24):13964-9 2003
PubMed ID: 14612561
 
Sharma DK, Choudhury A, Singh RD, Wheatley CL, Marks DL, Pagano RE, Glycosphingolipids internalized via caveolar-related endocytosis rapidly merge with the clathrin pathway in early endosomes and form microdomains for recycling. J Biol Chem278(9):7564-72 2003
PubMed ID: 12482757
 
Zhang J, Asin-Cayuela J, Fish J, Michikawa Y, Bonafe M, Olivieri F, Passarino G, De Benedictis G, Franceschi C, Attardi G, Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes. Proc Natl Acad Sci U S A100(3):1116-21 2003
PubMed ID: 12538859
 
Choudhury A, Dominguez M, Puri V, Sharma DK, Narita K, Wheatley CL, Marks DL, Pagano RE, Rab proteins mediate Golgi transport of caveola-internalized glycosphingolipids and correct lipid trafficking in Niemann-Pick C cells. J Clin Invest109(12):1541-50 2002
PubMed ID: 12070301
 
Sawkar AR, Cheng WC, Beutler E, Wong CH, Balch WE, Kelly JW, Chemical chaperones increase the cellular activity of N370S beta -glucosidase: a therapeutic strategy for Gaucher disease. Proc Natl Acad Sci U S A99(24):15428-33 2002
PubMed ID: 12434014
 
Desai SD, Li TK, Rodriguez-Bauman A, Rubin EH, Liu LF, Ubiquitin/26S proteasome-mediated degradation of topoisomerase I as a resistance mechanism to camptothecin in tumor cells. Cancer Res61(15):5926-32 2001
PubMed ID: 11479235
 
Tang Q, Edidin M, Vesicle trafficking and cell surface membrane patchiness. Biophys J81(1):196-203 2001
PubMed ID: 11423406
 
Chen CS, Bach G, Pagano RE, Abnormal transport along the lysosomal pathway in mucolipidosis, type IV disease. Proc Natl Acad Sci U S A95:6373-8 1998
PubMed ID: 9600972
 
Hwang J, Gheber LA, Margolis L, Edidin M, Domains in cell plasma membranes investigated by near-field scanning optical microscopy. Biophys J74:2184-90 1998
PubMed ID: 9591645
 
Ratner JN, Balasubramanian B, Corden J, Warren SL, Bregman DB, Ultraviolet radiation-induced ubiquitination and proteasomal degradation of the large subunit of RNA polymerase II. Implications for transcription-coupled DNA repair. J Biol Chem273(9):5184-9 1998
PubMed ID: 9478972
 
Villani G, Greco M, Papa S, Attardi G, Low reserve of cytochrome c oxidase capacity in vivo in the respiratory chain of a variety of human cell types. J Biol Chem273:31829-36 1998
PubMed ID: 9822650
 
Bregman DB, Halaban R, van Gool AJ, Henning KA, Friedberg EC, Warren SL, UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells. Proc Natl Acad Sci U S A93:11586-90 1996
PubMed ID: 8876179
 
Sass C, Giroux LM, Ma Y, Roy M, Lavigne J, Lussier-Cacan S, Davignon J, Minnich A, Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemia. Hum Genet96:21-6 1995
PubMed ID: 7607649
 
Vazquez F, Grider A, The effect of the acrodermatitis enteropathica mutation on zinc uptake in human fibroblasts. Biol Trace Elem Res50:109-17 1995
PubMed ID: 8605078
 
Ha VT, Marshall MK, Elsas LJ, Pinnell SR, Yeowell HN, A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene. J Clin Invest93:1716-21 1994
PubMed ID: 8163671
 
Yeowell HN, Ha V, Clark WL, Marshall MK, Pinnell SR, Sequence analysis of a cDNA for lysyl hydroxylase isolated from human skin fibroblasts from a normal donor: differences from human placental lysyl hydroxylase cDNA. J Invest Dermatol102:382-4 1994
PubMed ID: 8120423
 
Srivastava S, Wang S, Tong YA, Hao ZM, Chang EH, Dominant negative effect of a germ-line mutant p53: a step fostering tumorigenesis. Cancer Res53:4452-5 1993
PubMed ID: 8402611
 
Pienta KJ, Getzenberg RH, Coffey DS, Characterization of nuclear morphology and nuclear matrices in ageing human fibroblasts. Mech Ageing Dev62:13-24 1992
PubMed ID: 1560681
 
Kochevar IE, Walsh AA, Green HA, Sherwood M, Shih AG, Sutherland BM, DNA damage induced by 193-nm radiation in mammalian cells. Cancer Res51:288-93 1991
PubMed ID: 1988091
 
Markello TC, Guo J, Gahl WA, High-performance liquid chromatography of lipids for the identification of human metabolic disease. Anal Biochem198:368-74 1991
PubMed ID: 1799224
 
Zhong N, Martiniuk F, Tzall S, Hirschhorn R, Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele. Am J Hum Genet49:635-45 1991
PubMed ID: 1652892
 
Liscum L, Faust JR, The intracellular transport of low density lipoprotein-derived cholesterol is inhibited in Chinese hamster ovary cells cultured with 3-beta-[2-(diethylamino)ethoxy]androst-5-en-17-one. J Biol Chem264(20):11796-806 1989
PubMed ID: 2745416
 
Weiss MJ, Ray K, Fallon MD, Whyte MP, Fedde KN, Lafferty MA, Mulivor RA, Harris H, Analysis of liver/bone/kidney alkaline phosphatase mRNA, DNA, and enzymatic activity in cultured skin fibroblasts from 14 unrelated patients with severe hypophosphatasia. Am J Hum Genet44:686-94 1989
PubMed ID: 2705456
 
Chatterjee S, Ghosh N, Castiglione E, Kwiterovich PO Jr, Regulation of glycosphingolipid glycosyltransferase by low density lipoprotein receptors in cultured human proximal tubular cells. J Biol Chem263:13017-22 1988
PubMed ID: 2458339
 
Hutchins JT, Reading CL, Giavazzi R, Hoaglund J, Jessup JM, Distribution of mono-, di, and tri-O-acetylated sialic acids in normal and neoplastic colon. Cancer Res48:483-9 1988
PubMed ID: 3335016
 
Sephel GC, Sturrock A, Giro MG, Davidson JM, Increased elastin production by progeria skin fibroblasts is controlled by the steady-state levels of elastin mRNA. J Invest Dermatol90:643-7 1988
PubMed ID: 3361140
 
Liscum L, Faust JR, Low density lipoprotein (LDL)-mediated suppression of cholesterol synthesis and LDL uptake is defective in Niemann-Pick type C fibroblasts. J Biol Chem262:17002-8 1987
PubMed ID: 3680287
 
Hinman LM, Ksiezak-Reding H, Baker AC, Blass JP, Pigeon liver phosphoprotein phosphatase: an effective activator of pyruvate dehydrogenase in tissue homogenates. Arch Biochem Biophys246:381-90 1986
PubMed ID: 3008658
 
Miller AC, Henderson BW, The influence of cellular glutathione content on cell survival following photodynamic treatment in vitro. Radiat Res107:83-94 1986
PubMed ID: 2942963
 
Pentchev PG, Comly ME, Kruth HS, Patel S, Proestel M, Weintroub H, The cholesterol storage disorder of the mutant BALB/c mouse. A primary genetic lesion closely linked to defective esterification of exogenously derived cholesterol and its relationship to human type C Niemann-Pick disease. J Biol Chem261:2772-7 1986
PubMed ID: 3949747
 
Sephel GC, Davidson JM, Elastin production in human skin fibroblast cultures and its decline with age. J Invest Dermatol86:279-85 1986
PubMed ID: 3745952
 
Coates PM, Hale DE, Stanley CA, Corkey BE, Cortner JA, Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Pediatr Res19:671-6 1985
PubMed ID: 4022673

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