共 50 条
- [31] Systemic Gene Replacement Therapy Corrects Neurological Phenotype in a Mouse Model of NGLY1 DeficiencyMOLECULAR THERAPY, 2024, 32 (04) : 745 - 745Du, Ailing论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USAZhou, Xuntao论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Dept Microbiol & Physiol Syst, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USARen, Lingzhi论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USALiu, Nan论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USAZhou, Chen论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USALiang, Jialing Yang论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USAGao, Guangping论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, Dept Microbiol & Physiol Syst, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USAWang, Dan论文数: 0 引用数: 0 h-index: 0机构: UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA UMass Chan Med Sch, RNA Therapeut Inst, Worcester, MA USA UMass Chan Med Sch, Horae Gene Therapy Ctr, Worcester, MA USA
- [32] AAV9-NGLY1 gene replacement therapy improves phenotypic and biomarker endpoints in a rat model of NGLY1 DeficiencyMOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 2022, 27 : 259 - 271Zhu, Lei论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USATan, Brandon论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USADwight, Selina S.论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USABeahm, Brendan论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USAWilsey, Matt论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USACrawford, Brett E.论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USASchweighardt, Becky论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USACook, Jennifer W.论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USAWechsler, Thomas论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USAMueller, William F.论文数: 0 引用数: 0 h-index: 0机构: Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA Grace Sci LLC, 1142 Crane St,Ste 4, Menlo Pk, CA 94025 USA
- [33] Mutations in NGLY1 gene linked with new genetic disorderAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (07)Levenson, Deborah论文数: 0 引用数: 0 h-index: 0
- [34] A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiencyELIFE, 2020, 9 : 1 - 22Talsness, Dana M.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAOwings, Katie G.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USACoelho, Emily论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAMercenne, Gaelle论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Internal Med, Div Nephrol & Hypertens, Salt Lake City, UT 84112 USA Univ Utah, Mol Med Program, Salt Lake City, UT USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAPleinis, John M.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Internal Med, Div Nephrol & Hypertens, Salt Lake City, UT 84112 USA Univ Utah, Mol Med Program, Salt Lake City, UT USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAPartha, Raghavendran论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Computat & Syst Biol, Pittsburgh, PA USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAHope, Kevin A.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAZuberi, Aamir R.论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Genet Resource Sci, 600 Main St, Bar Harbor, ME 04609 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAClark, Nathan L.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USALutz, Cathleen M.论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Genet Resource Sci, 600 Main St, Bar Harbor, ME 04609 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USARodan, Aylin R.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Internal Med, Div Nephrol & Hypertens, Salt Lake City, UT 84112 USA Univ Utah, Mol Med Program, Salt Lake City, UT USA Vet Affairs Salt Lake City Hlth Care Syst, Med Serv, Salt Lake City, UT USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USAChow, Clement Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA Univ Utah, Sch Med, Dept Human Genet, Salt Lake City, UT 84132 USA
- [35] Ocular features of NGLY1 deficiency from a prospective longitudinal cohortJOURNAL OF AAPOS, 2024, 28 (03):Frater, Christina H.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USA Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USARuzhnikov, Maura R. Z.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USA Stanford Univ, Div Med Genet, Palo Alto, CA USA Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USABeres, Shannon论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USA Stanford Univ, Byers Eye Inst, Dept Ophthalmol, Palo Alto, CA USA Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USAAlcorn, Deborah论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Byers Eye Inst, Dept Ophthalmol, Palo Alto, CA USA Stanford Univ, Dept Pediat, Palo Alto, CA USA Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USAShue, Ann论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Byers Eye Inst, Dept Ophthalmol, Palo Alto, CA USA Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USALevy, Rebecca J.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USA Stanford Univ, Neurol & Neurol Sci, Palo Alto, CA USA
- [36] NGLY1 Deficiency: A Rare Newly Described Condition with a Typical PresentationLIFE-BASEL, 2021, 11 (03):Dabaj, Ivana论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceSudrie-Arnaud, Benedicte论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Metab Biochem, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceLecoquierre, Francois论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Genet, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Reference Ctr Dev Disorders, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceRaymond, Kimiyo论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55902 USA Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceDucatez, Franklin论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceGuerrot, Anne-Marie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Genet, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Reference Ctr Dev Disorders, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceSnanoudj, Sarah论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Metab Biochem, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceCoutant, Sophie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Genet, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Reference Ctr Dev Disorders, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceSaugier-Veber, Pascale论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Genet, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Reference Ctr Dev Disorders, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceMarret, Stephane论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceNicolas, Gael论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Genet, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Reference Ctr Dev Disorders, INSERM U1245, UNIROUEN,CHU Rouen,FHU G4 Genom, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceTebani, Abdellah论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Metab Biochem, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, FranceBekri, Soumeya论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Dept Metab Biochem, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France Normandie Univ, Dept Neonatal Pediat Intens Care & Neuropediat, INSERM U1245, UNIROUEN,CHU Rouen, F-76000 Rouen, France
- [37] Correction to: Reversibility of motor dysfunction in the rat model of NGLY1 deficiencyMolecular Brain, 14Makoto Asahina论文数: 0 引用数: 0 h-index: 0机构: T-CiRA Discovery,Glycometabolic Biochemistry LaboratoryReiko Fujinawa论文数: 0 引用数: 0 h-index: 0机构: T-CiRA Discovery,Glycometabolic Biochemistry LaboratoryHiroto Hirayama论文数: 0 引用数: 0 h-index: 0机构: T-CiRA Discovery,Glycometabolic Biochemistry LaboratoryRyuichi Tozawa论文数: 0 引用数: 0 h-index: 0机构: T-CiRA Discovery,Glycometabolic Biochemistry LaboratoryYasushi Kajii论文数: 0 引用数: 0 h-index: 0机构: T-CiRA Discovery,Glycometabolic Biochemistry LaboratoryTadashi Suzuki论文数: 0 引用数: 0 h-index: 0机构: T-CiRA Discovery,Glycometabolic Biochemistry Laboratory
- [38] Clarifying the phenotype of NGLY1 deficiency, the first congenital disorder of deglycosylationMOLECULAR GENETICS AND METABOLISM, 2015, 114 (03) : 315 - 316Lam, Christina论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genet Branch, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAFerreira, Carlos论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genet Branch, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAKrasnewich, Donna论文数: 0 引用数: 0 h-index: 0机构: NIGMS, Div Genet & Dev Biol, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAToro, Camillo论文数: 0 引用数: 0 h-index: 0机构: NIH, Undiagnosed Dis Program, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USALatham, Lea论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Off Clin Director, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAZein, Wadih论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Clin Genet Sect, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USALehky, Tanya论文数: 0 引用数: 0 h-index: 0机构: NINDS, Electromyog Sect, Bethesda, MD 20892 USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USABrewer, Carmen论文数: 0 引用数: 0 h-index: 0机构: NIDCD, Otolcayngol Branch, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAKing, Kelly论文数: 0 引用数: 0 h-index: 0机构: NIDCD, Otolcayngol Branch, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAWassif, Christopher论文数: 0 引用数: 0 h-index: 0机构: NIDCD, Otolcayngol Branch, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USARosenzweig, Sergio论文数: 0 引用数: 0 h-index: 0机构: NIH, CC, Serv Immunol, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USALyons, Jonathan论文数: 0 引用数: 0 h-index: 0机构: NIAID, Genet & Pathogenesis Allergy Sect, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAGahl, William论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genet Branch, NIH, Bethesda, MD USA NIH, Undiagnosed Dis Program, Bethesda, MD USA NHGRI, Off Clin Director, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USAWolfe, Lynne论文数: 0 引用数: 0 h-index: 0机构: NIH, Undiagnosed Dis Program, Bethesda, MD USA NHGRI, Off Clin Director, NIH, Bethesda, MD USA NHGRI, Med Genet Branch, NIH, Bethesda, MD USA
- [39] Evidence for hyperactivation of innate immunity in a Drosophila model of NGLY1 deficiencyGLYCOBIOLOGY, 2021, 31 (12) : 1715 - 1716Pandey, Ashutosh论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USA Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USAHan, Seung Yeop论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USA Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USAMueller, William F.论文数: 0 引用数: 0 h-index: 0机构: European Mol Biol Lab EMBL, Genome Biol Unit, Heidelberg, Germany Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USAStory, Benjamin A.论文数: 0 引用数: 0 h-index: 0机构: European Mol Biol Lab EMBL, Genome Biol Unit, Heidelberg, Germany Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USA论文数: 引用数: h-index:机构:Steinmetz, Lars论文数: 0 引用数: 0 h-index: 0机构: European Mol Biol Lab EMBL, Genome Biol Unit, Heidelberg, Germany Stanford Univ, Sch Med, Dept Genet, Stanford, CA USA Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USAJafar-Nejad, Hamed论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USA Baylor Coll Med, Dept Human & Mol Genet, Houston, TX USA
- [40] NGLY1 mutations cause protein aggregation in human neuronsCELL REPORTS, 2023, 42 (12):Manole, Andreea论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA论文数: 引用数: h-index:机构:Rhee, Amanda论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USANovak, Sammy论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Waitt Adv Biophoton Core, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAChin, Shao-Ming论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USATsimring, Katya论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAPaucar, Andres论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA论文数: 引用数: h-index:机构:Newmeyer, Traci Fang论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USASchafer, Simon T.论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USARosh, Idan论文数: 0 引用数: 0 h-index: 0机构: Univ Haifa, Fac Nat Sci, Sagol Dept Neurobiol, Haifa, Israel Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAKaushik, Susmita论文数: 0 引用数: 0 h-index: 0机构: Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA Albert Einstein Coll Med, Inst Aging Studies, Bronx, NY 10461 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAHoffman, Rene论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAChen, Songjie论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAWang, Guangwen论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA论文数: 引用数: h-index:机构:Cuervo, Ana Maria论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAAndrade, Leo论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAManor, Uri论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Waitt Adv Biophoton Core, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USALee, Kevin论文数: 0 引用数: 0 h-index: 0机构: Grace Sci Fdn, Menlo Pk, CA 94025 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAJones, Jeffrey R.论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAStern, Shani论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAMarchetto, Maria C.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Dept Anthropol, La Jolla, CA 92093 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USAGage, Fred H.论文数: 0 引用数: 0 h-index: 0机构: Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA Salk Inst Biol Studies, Lab Genet, 10010 North Torrey Pines Rd, La Jolla, CA 92037 USA