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1. Full Text G protein-coupled receptor kinase 3 and protein kinase C phosphorylate the distal C-terminal tail of the chemokine receptor CXCR4 and mediate recruitment of β-arrestin
by Luo, Jiansong and Busillo, John M and Stumm, Ralf and Benovic, Jeffrey L
Molecular Pharmacology, ISSN 0026-895X, 06/2017, Volume 91, Issue 6, pp. 554 - 566
Phosphorylation of G protein-coupled receptors (GPCRs) is a key event for cell signaling and regulation of receptor function. Previously, using tandem mass... 
GPCR PHOSPHORYLATION | M-ZETA | INTERNALIZATION | ACTIVATION | OPIOID RECEPTOR | PHARMACOLOGY | WHIM SYNDROME | SDF-1 | PHARMACOLOGY & PHARMACY | CELL | MICE LACKING | Phosphorylation - physiology | Humans | beta-Arrestins - metabolism | Protein Kinase C - antagonists & inhibitors | G-Protein-Coupled Receptor Kinase 3 - metabolism | Serine - metabolism | Receptors, CXCR4 - metabolism | Isoenzymes - metabolism | Protein Kinase C - metabolism | HEK293 Cells | Protein Kinase Inhibitors - pharmacology | Phosphorylation - drug effects | Isoenzymes - antagonists & inhibitors | Index Medicus
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2. Full Text Missing-in-metastasis protein downregulates CXCR4 by promoting ubiquitylation and interaction with small Rab GTPases
by Li, Lushen and Baxter, Shaneen S and Gu, Ning and Ji, Min and Zhan, Xi
Journal of Cell Science, ISSN 0021-9533, 04/2017, Volume 130, Issue 8, pp. 1475 - 1485
Surface expression of chemokine receptor CXCR4 is downregulated by missing-in-metastasis protein (MIM; also known as MTSS1), a member of the inverse BAR... 
MIM | CXCR4 | AIP4 | Rab7 | Ubiquitylation | MVBs | COUPLED RECEPTOR CXCR4 | WW DOMAINS | BLADDER-CANCER | TRAFFICKING | SUPPRESSOR 1 MTSS1 | ENDOCYTOSIS | CELL BIOLOGY | UBIQUITINATION | CHEMOKINE RECEPTORS | EXPRESSION | rab GTP-Binding Proteins - metabolism | Down-Regulation | Humans | Neoplasm Proteins - immunology | Neoplasm Proteins - metabolism | Endosomes - metabolism | Mice, Knockout | Protein Transport | Receptors, CXCR4 - metabolism | Ubiquitination | Animals | Chemokine CXCL12 - metabolism | Transport Vesicles - metabolism | Microfilament Proteins - immunology | Protein Binding | Endocytosis - genetics | Mice | Microfilament Proteins - metabolism | HeLa Cells | Neoplasm Proteins - genetics | Microfilament Proteins - genetics | Coils | Ubiquitin | GTP-binding protein | Membranes | CXCL12 protein | Trafficking | Metastasis | SDF-1 protein | CXCR4 protein | Metastases | Proteins | Clonal deletion | Rab5 protein | Internalization | Deletion | Protein transport | Curvature | Ubiquitin-protein ligase | Cytoplasm | Guanosinetriphosphatase
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3. Full Text Local CXCR4 Upregulation in the Injured Arterial Wall Contributes to Intimal Hyperplasia
by Shi, Xudong and Guo, Lian‐Wang and Seedial, Stephen and Takayama, Toshio and Wang, Bowen and Zhang, Mengxue and Franco, Sarah R and Si, Yi and Chaudhary, Mirnal A and Liu, Bo and Kent, K. Craig
STEM CELLS, ISSN 1066-5099, 11/2016, Volume 34, Issue 11, pp. 2744 - 2757
CXCR4 is a stem/progenitor cell surface receptor specific for the cytokine stromal cell‐derived factor‐1 (SDF‐1α). There is evidence that bone marrow‐derived... 
CXCR4/SDF‐1α | smooth muscle cell specific CXCR4 knockout | intimal hyperplasia | TGFβ/Smad3 | smooth muscle cell migration | CXCR4/SDF-1α | PROGENITOR CELLS | TGF-BETA | TGF beta/Smad3 | CHEMOKINE RECEPTOR CXCR4 | SDF-1-ALPHA/CXCR4 AXIS | NEOINTIMAL HYPERPLASIA | DEPENDENT PATHWAYS | CXCR4/SDF-1 alpha | CELL & TISSUE ENGINEERING | CELL BIOLOGY | VASCULAR INJURY | GROWTH-FACTOR-BETA | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CANCER METASTASIS | SMOOTH-MUSCLE-CELLS | HEMATOLOGY | Carotid Arteries - metabolism | Phosphorylation | Male | Smad3 Protein - metabolism | Smad3 Protein - genetics | Neointima - genetics | Mitogen-Activated Protein Kinase 1 - genetics | Receptors, CXCR4 - deficiency | Muscle Proteins - metabolism | Receptors, CXCR4 - genetics | Carotid Artery Injuries - genetics | Microfilament Proteins - metabolism | Myocytes, Smooth Muscle - drug effects | Microfilament Proteins - genetics | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Carotid Artery Injuries - metabolism | Carotid Artery Injuries - pathology | Promoter Regions, Genetic | Mitogen-Activated Protein Kinase 3 - genetics | Signal Transduction | Gene Expression Regulation | Rats | Neointima - metabolism | Rats, Sprague-Dawley | Tunica Intima - injuries | Mice, Knockout | Muscle Proteins - genetics | Tunica Intima - metabolism | Transforming Growth Factor beta - pharmacology | Animals | Mitogen-Activated Protein Kinase 3 - metabolism | Neointima - pathology | Mice | Primary Cell Culture | Transforming Growth Factor beta - metabolism | Cell Movement | Mitogen-Activated Protein Kinase 1 - metabolism | Bone morphogenetic proteins | RNA | Transforming growth factors | Hyperplasia | Stem cells | Rodents | Cell adhesion & migration | Chromatin | Femur | Immunoprecipitation | Leukocyte migration | Transforming growth factor-b | Stem cell transplantation | Smooth muscle | Smad3 protein | Wire | Assaying | Cell surface | Carotid arteries | Arteries | Homing | Protein folding | Bone marrow | Carotid artery | Therapeutic applications | Extracellular signal-regulated kinase | SDF-1 protein | CXCR4 protein | Restenosis | Injury prevention | Cell migration | Smad3 | SDF‐1α | TGFβ | CXCR4 | Tissue‐Specific Stem Cells
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4. Full Text PPI‐Detect: A support vector machine model for sequence‐based prediction of protein–protein interactions
by Romero‐Molina, Sandra and Ruiz‐Blanco, Yasser B and Harms, Mirja and Münch, Jan and Sanchez‐Garcia, Elsa
Journal of Computational Chemistry, ISSN 0192-8651, 04/2019, Volume 40, Issue 11, pp. 1233 - 1242
The prediction of peptide–protein or protein–protein interactions (PPI) is a challenging task, especially if amino acid sequences are the only information... 
protein–protein interactions | ProtDCal | EPI‐X4 | G‐protein‐coupled receptor | CXCR4 | PPI‐Detect | protein descriptor | DESCRIPTOR | DOMAIN | INFORMATION | G-protein-coupled receptor | SDF-1 | LESTR/FUSIN | EPI-X4 | CHEMISTRY, MULTIDISCIPLINARY | DISCOVERY | protein-protein interactions | PEPTIDES | PPI-Detect | DATABASE | WEB SERVER | Proteins | Amino acids | Data mining | Protein-protein interactions | Machine learning
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5. Full Text β-Arrestin- but Not G Protein-Mediated Signaling by the "Decoy" Receptor CXCR7
by Sudarshan Rajagopal and Jihee Kim and Seungkirl Ahn and Stewart Craig and Christopher M. Lam and Norma P. Gerard and Craig Gerard and Robert J. Lefkowitz
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2010, Volume 107, Issue 2, pp. 628 - 632
Ubiquitously expressed seven-transmembrane receptors (7TMRs) classically signal through heterotrimeric G proteins and are commonly referred to as G... 
Receptors | Transfection | HEK293 cells | Calcium | Antibodies | Small interfering RNA | Ligands | Agonists | Chemokine receptors | Chemokines | Chemokine | G protein-coupled receptors | Seven-transmembrane receptor | Biased receptor | PATHWAYS | chemokine | CHEMOTAXIS | BETA-ARRESTIN-2 | MULTIDISCIPLINARY SCIENCES | COUPLED RECEPTOR | ERK1/2 ACTIVATION | MAPK ACTIVATION | CXCL12/SDF-1 | biased receptor | CELL-MIGRATION | CHEMOKINE RECEPTOR | LIGAND | seven-transmembrane receptor | Cell Line | T-Lymphocytes - physiology | GTP-Binding Proteins - physiology | Phosphorylation | Receptors, CXCR - genetics | Humans | RNA, Messenger - genetics | Arrestins - physiology | Rats | Extracellular Signal-Regulated MAP Kinases - metabolism | GTP-Binding Proteins - genetics | Animals | T-Lymphocytes - cytology | beta-Arrestins | Signal Transduction - physiology | Mice | Enzyme Activation | Receptors, CXCR - physiology | Receptors, Chemokine - genetics | Muscle, Smooth, Vascular - physiology
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6. Full Text CXCR7 functions as a scavenger for CXCL12 and CXCL11
by Naumann, Ulrike and Cameroni, Elisabetta and Pruenster, Monika and Mahabaleshwar, Harsha and Raz, Erez and Zerwes, Hans-Günter and Rot, Antal and Thelen, Marcus
PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, p. e9175
Background: CXCR7 (RDC1), the recently discovered second receptor for CXCL12, is phylogenetically closely related to chemokine receptors, but fails to couple... 
MIGRATION | CELL-DERIVED FACTOR-1-ALPHA | IN-VITRO | ACTIVATION | CHEMOKINE RECEPTOR CXCR4 | ENDOTHELIAL-CELLS | BIOLOGY | SDF-1 | LIGAND | PROTEIN-KINASE B | T-LYMPHOCYTES | Chemokine CXCL11 - genetics | Humans | Embryo, Nonmammalian - metabolism | Male | Green Fluorescent Proteins - genetics | Recombinant Fusion Proteins - metabolism | Chemokine CXCL12 - genetics | Flow Cytometry | Transfection | Receptors, CXCR - metabolism | Myocardium - metabolism | Female | Cell Membrane - metabolism | Receptors, CXCR - physiology | Cell Line | Green Fluorescent Proteins - metabolism | Endothelial Cells - metabolism | Receptors, CXCR - genetics | Cells, Cultured | Zebrafish | Endocytosis - physiology | Microscopy, Confocal | Animals | Chemokine CXCL12 - metabolism | Endothelial Cells - cytology | Cell Line, Tumor | Recombinant Fusion Proteins - genetics | Ligands | Mice | Mice, Inbred BALB C | HeLa Cells | Chemokine CXCL11 - metabolism | Proteins | B cells | Heart | CXCL12 protein | Biomedical research | Amino acids | Metastasis | Phylogeny | Kinases | Human tissues | Cell adhesion & migration | Mammalian cells | Degradation | Signal transduction | Receptors | Rodents | Animal tissues | Penicillin | Bone marrow | Organs | Mammals | Embryos | Chemokine receptors | CXCR4 protein | Hemopoiesis | Endothelium | Signaling | Plasmids | Internalization | CXCL11 protein | Mutation | Umbilical vein | Prostate cancer | Chemokines
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7. Full Text Structure-Based Identification of Novel Ligands Targeting Multiple Sites within a Chemokine-G-Protein-Coupled-Receptor Interface
by Smith, Emmanuel W and Nevins, Amanda M and Qiao, Zhen and Liu, Yan and Getschman, Anthony E and Vankayala, Sai L and Kemp, M. Trent and Peterson, Francis C and Li, Rongshi and Volkman, Brian F and Chen, Yu
Journal of Medicinal Chemistry, ISSN 0022-2623, 05/2016, Volume 59, Issue 9, pp. 4342 - 4351
CXCL12 is a human chemokine that recognizes the CXCR4 receptor and is involved in immune responses and metastatic cancer. Interactions between CXCL12 and CXCR4... 
CXCR4 SULFOTYROSINE | CHEMISTRY, MEDICINAL | RECOGNITION | DOCKING | DRUG DESIGN | MONOMER-DIMER EQUILIBRIUM | SDF-1/CXCL12 | RESIDUES | DISCOVERY | BINDING HOT-SPOTS | CONFORMATIONS | Chemokine CXCL12 - metabolism | Magnetic Resonance Spectroscopy | Humans | Ligands | Molecular Structure | Binding Sites | Receptors, CXCR4 - metabolism
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8. Full Text Photoactivatable Chemokines – Controlling Protein Activity by Light
by Baumann, Lars and Beck‐Sickinger, Annette G
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2013, Volume 52, Issue 36, pp. 9550 - 9553
Activation by light : Caged depsipeptides are incorporated as photoresponsive elements into the backbone of the protein SDF‐1α by using expressed protein... 
expressed protein ligation | peptides | protein engineering | photoactivation | ligation reactions | ACIDS | SDF-1 | RECEPTOR | PHASE PEPTIDE-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | CLICK PEPTIDE | IN-VITRO | CLONING | CXCR4 ACTIVATION | BINDING | SWITCH-PEPTIDES | Chemokines - chemistry | Chemokine CXCL12 - chemistry | Jurkat Cells | Humans | Light | Luminescent Proteins - chemistry | Models, Molecular | Chromatography, High Pressure Liquid | Chemokines - radiation effects | Peptides | Backbone | Proteins | Activation | Restoration
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9. Full Text CXCL12 induces connective tissue growth factor expression in human lung fibroblasts through the Rac1/ERK, JNK, and AP-1 pathways
by Lin, Chien-Huang and Shih, Chung-Huang and Tseng, Chih-Chieh and Yu, Chung-Chi and Tsai, Yuan-Jhih and Bien, Mauo-Ying and Chen, Bing-Chang
PLoS ONE, ISSN 1932-6203, 08/2014, Volume 9, Issue 8, p. e104746
CXCL12 (stromal cell-derived factor-1, SDF-1) is a potent chemokine for homing of CXCR4(+) fibrocytes to injury sites of lung tissue, which contributes to... 
REGULATED KINASE | SIGNALING AXIS | CANCER CELLS | EPITHELIAL-CELLS | MULTIDISCIPLINARY SCIENCES | GENE-REGULATION | CIRCULATING FIBROCYTES | FACTOR-I | IDIOPATHIC PULMONARY-FIBROSIS | NF-KAPPA-B | FOCAL ADHESIONS | Cell Line | Chemokine CXCL12 - physiology | Fibroblasts - enzymology | Phosphorylation | Humans | Actins - metabolism | rac GTP-Binding Proteins - metabolism | Extracellular Signal-Regulated MAP Kinases - metabolism | DNA Primers | Lung - cytology | Transcription Factor AP-1 - metabolism | Lung - enzymology | Receptors, CXCR4 - metabolism | MAP Kinase Kinase 4 - metabolism | Base Sequence | Polymerase Chain Reaction | Connective Tissue Growth Factor - genetics | Lung - metabolism | Connective Tissue Growth Factor - metabolism | Fibroblasts - metabolism | Muscle proteins | Respiratory tract diseases | Luciferase | CXCL12 protein | Transcription factors | Smooth muscle | Kinases | Cell adhesion & migration | Proteins | Homing | Connective tissues | Pathways | Actin | Fibroblasts | Curcumin | Inhibition | Growth factors | c-Fos protein | Respiratory therapy | Phenotypes | Internal medicine | Lung diseases | Activator protein 1 | Muscles | Extracellular signal-regulated kinase | c-Jun protein | p21-activated kinase | MAP kinase | Connective tissue growth factor | Rac1 protein | siRNA | Gene expression | SDF-1 protein | Ribonucleic acid--RNA | CXCR4 protein | Medicine | Signaling | Pulmonary fibrosis | Inhibitors | Protein kinase | Fibrosis | Cell migration | Chemokines | RNA | Ribonucleic acid
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10. Full Text The Lim1 oncogene as a new therapeutic target for metastatic human renal cell carcinoma
by Hamaidi, Imène and Coquard, Catherine and Danilin, Sabrina and Dormoy, Valérian and Béraud, Claire and Rothhut, Sylvie and Barthelmebs, Mariette and Benkirane-Jessel, Nadia and Lindner, Véronique and Lang, Hervé and Massfelder, Thierry
Oncogene, ISSN 0950-9232, 01/2019, Volume 38, Issue 1, pp. 60 - 72
Metastatic clear cell renal cell carcinoma (CCC) remains incurable despite advances in the development of anti-angiogenic targeted therapies and the emergence... 
LDB1 | ONCOLOGY | PATHWAY | LHX1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE | GROWTH | GENETICS & HEREDITY | DIFFERENTIATION | EXPRESSION | REQUIREMENT | CELL BIOLOGY | RNA, Small Interfering - genetics | Kidney Neoplasms - genetics | Humans | Neoplasm Proteins - physiology | Gene Expression Regulation, Neoplastic | Carcinoma, Renal Cell - genetics | Neoplasm Proteins - antagonists & inhibitors | LIM-Homeodomain Proteins - antagonists & inhibitors | Molecular Targeted Therapy | Gene Knockdown Techniques | Lung Neoplasms - secondary | RNA Interference | Epithelial-Mesenchymal Transition | Neoplasm Proteins - genetics | Kidney Neoplasms - therapy | Oncogenes | Transcription Factors - physiology | Signal Transduction | Neoplasm Invasiveness | Von Hippel-Lindau Tumor Suppressor Protein - physiology | Transcription Factors - antagonists & inhibitors | Lung Neoplasms - therapy | Transcription Factors - genetics | LIM-Homeodomain Proteins - genetics | Lung Neoplasms - prevention & control | RNA, Small Interfering - therapeutic use | Carcinoma, Renal Cell - secondary | Carcinoma, Renal Cell - therapy | Cell Line, Tumor | LIM-Homeodomain Proteins - physiology | Cell Movement | Complications and side effects | Care and treatment | Transcription factors | Genetic aspects | Carcinoma, Renal cell | Metastasis | Gene expression | Health aspects | Risk factors | Cell proliferation | Intravenous administration | Mesenchyme | Fibronectin | Lymph nodes | Metastases | Cell adhesion & migration | Angiogenesis | Signal transduction | Cell adhesion | Gene transfer | Therapeutic applications | siRNA | SDF-1 protein | CXCR4 protein | Immune checkpoint | Hedgehog protein | Kidney cancer | Cell lines | Tumor suppressor genes | VHL protein | Skin | Neoplasia | Paxillin | Cell migration | Clear cell-type renal cell carcinoma | Apoptosis
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11. Full Text Targeting AU-rich element-mediated mRNA decay with a truncated active form of the zinc-finger protein TIS11b/BRF1 impairs major hallmarks of mammary tumorigenesis
by Rataj, Felicitas and Planel, Séverine and Denis, Josiane and Roelants, Caroline and Filhol, Odile and Guyon, Laurent and Feige, Jean-Jacques and Cherradi, Nadia
Oncogene, ISSN 0950-9232, 06/2019, Volume 38, Issue 26, pp. 5174 - 5190
Altered expression of regulatory RNA-binding proteins (RBPs) in cancer leads to abnormal expression of mRNAs encoding many factors involved in cancer... 
TIMP-1 | TRISTETRAPROLIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING PROTEIN | CXCR4/CXCL12 AXIS | CELL BIOLOGY | BREAST-CANCER | TTP | ONCOLOGY | DESTABILIZATION | SEQUENCE | GROWTH | GENETICS & HEREDITY | EXPRESSION | Enzymes | Care and treatment | Messenger RNA | Aspartate | Drug resistance | Health aspects | Vascular endothelial growth factor | Protein binding | Tumors | Cancer | Vimentin | CXCL12 protein | Mesenchyme | Medical innovations | Serine | Cell fusion | Proteins | N-Cadherin | Clonal deletion | Fractalkine | Tumorigenesis | Fusion protein | Pentraxins | Secretion | mRNA turnover | Breast cancer | Tumor cell lines | SDF-1 protein | Cadherin | Endothelial cells | RNA-binding protein | Cell lines | Hypoxia | Monocyte chemoattractant protein 1 | Chemokines | Life Sciences
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12. Full Text A multifunctional multimaterial system for on-demand protein release
by Tuncaboylu, Deniz Ceylan and Friess, Fabian and Wischke, Christian and Lendlein, Andreas
Journal of Controlled Release, ISSN 0168-3659, 08/2018, Volume 284, pp. 240 - 247
In order to provide best control of the regeneration process for each individual patient, the release of protein drugs administered during surgery may need to... 
Proteins | On-demand release | Poly(ɛ-caprolactone) networks | Near infrared light triggered shape-recovery | Shape-memory polymer | Poly(epsilon-caprolactone) networks | MATRIX | HYDROGELS | DRUG-DELIVERY | SDF-1 | CHEMISTRY, MULTIDISCIPLINARY | NANOPARTICLES | REPAIR | PHARMACOLOGY & PHARMACY | GROWTH-FACTOR | Product introduction | Biological products
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13. Full Text Structural Basis of the Interaction between Chemokine Stromal Cell-derived Factor-1/CXCL12 and Its G-protein-coupled Receptor CXCR4
by Yutaka Kofuku and Chie Yoshiura and Takumi Ueda and Hiroaki Terasawa and Takahiro Hirai and Sae Tominaga and Masako Hirose and Yoshitake Maeda and Hideo Takahashi and Yuya Terashima and Kouji Matsushima and Ichio Shimada
Journal of Biological Chemistry, ISSN 0021-9258, 12/2009, Volume 284, Issue 50, pp. 35240 - 35250
The chemokine stromal cell-derived factor-1 (SDF-1/CXCL12) and its G-protein-coupled receptor (GPCR) CXCR4 play fundamental roles in many physiological... 
CORECEPTOR | FACTOR-1-ALPHA | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HIV-1 ENTRY | DIMERIZATION | MONOMER-DIMER EQUILIBRIUM | FUNCTIONAL-CHARACTERIZATION | CROSS-SATURATION EXPERIMENTS | FACTOR-I | LIGAND | Protein Structure, Tertiary | Chemokine CXCL12 - chemistry | Chemokine CXCL12 - genetics | Chemokine CXCL12 - metabolism | Humans | Models, Molecular | Nuclear Magnetic Resonance, Biomolecular | Receptors, CXCR4 - genetics | Structure-Activity Relationship | Receptors, CXCR4 - chemistry | Receptors, CXCR4 - metabolism | CXCL12 protein | G protein-coupled receptors | Purification | Crystallization | Data processing | Guanine nucleotide-binding protein | SDF-1 protein | CXCR4 protein | Metastases | Infection | N.M.R | Signal transduction | Chemokines | Cancer | Protein Structure and Folding
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14. Full Text Stem cell plasticity revisited: CXCR4-positive cells expressing mRNA for early muscle, liver and neural cells 'hide out' in the bone marrow
by Ratajczak, M.Z and Kucia, M and Reca, R and Majka, M and Janowska-Wieczorek, A and Ratajczak, J
Leukemia, ISSN 0887-6924, 01/2004, Volume 18, Issue 1, pp. 29 - 40
It has been suggested that bone marrow (BM)-derived hematopoietic stem cells transdifferentiate into tissue-specific stem cells (the so-called phenomenon of... 
SDF-1 | CXCR4 | Stem cell mobilization | Stem cell homing | Stem cell plasticity | stem cell plasticity | PROGENITOR CELLS | stem cell mobilization | FUSION | CHEMOKINE RECEPTOR CXCR4 | stem cell homing | PERIPHERAL-BLOOD | FACTOR-I | MICE LACKING | SKELETAL-MUSCLE | EPITHELIAL-CELLS | ONCOLOGY | STEM/PROGENITOR CELLS | HEMATOLOGY | Glial Fibrillary Acidic Protein - genetics | Nestin | Antigens, CD34 - metabolism | MyoD Protein - genetics | Humans | Blood Cells - metabolism | Muscle, Skeletal - metabolism | Glial Fibrillary Acidic Protein - metabolism | RNA, Messenger - metabolism | Blood Cells - cytology | Keratins - metabolism | Bone Marrow - metabolism | Intermediate Filament Proteins - genetics | Muscle Proteins - metabolism | Female | Neurons - metabolism | Hematopoietic Stem Cell Mobilization | DNA-Binding Proteins | alpha-Fetoproteins - metabolism | Hematopoietic Stem Cells - drug effects | Cell Line | Chemokine CXCL12 | alpha-Fetoproteins - genetics | Liver - metabolism | RNA, Messenger - genetics | Trans-Activators | Biomarkers - analysis | Hematopoietic Stem Cells - metabolism | MyoD Protein - metabolism | Nerve Tissue Proteins | Biomarkers - blood | Myogenic Regulatory Factor 5 | Chemokines, CXC - genetics | Receptors, CXCR4 - metabolism | Muscle Proteins - genetics | Granulocyte Colony-Stimulating Factor - pharmacology | Animals | Chemokines, CXC - metabolism | Mice | Mice, Inbred BALB C | Keratins - genetics | Intermediate Filament Proteins - metabolism
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