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Stem Cell Therapy for Craniofacial Bone Regeneration: A Randomized, Controlled Feasibility Trial

Cell transplantation, 2013-01, Vol.22 (5), p.767-777

2013

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Isolated bilateral macrostomia: literature review and case report

European journal of paediatric dentistry, 2023-02, Vol.24 (1), p.56

2023

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Standardization and Safety of Alveolar Bone–derived Stem Cell Isolation

Journal of dental research, 2014-01, Vol.93 (1), p.55-61

2014

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Stem cells derived from tooth periodontal ligament enhance functional angiogenesis by endothelial cells

Tissue engineering. Part A, 2014-04, Vol.20 (7-8), p.1188-1196

2014

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Tooth Storage, Dental Pulp Stem Cell Isolation, and Clinical Scale Expansion without Animal Serum

Journal of endodontics, 2014-05, Vol.40 (5), p.652-657

2014

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Angiogenic and osteogenic potential of bone repair cells for craniofacial regeneration

Tissue engineering. Part A, 2010-09, Vol.16 (9), p.2809-2820

2010

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Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease

Cell, 2015-04, Vol.161 (3), p.634-646

2015

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Development of a serum-free system to expand dental-derived stem cells: PDLSCs and SHEDs

Journal of cellular physiology, 2011-01, Vol.226 (1), p.66-73

2011

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Dental Pulp Tissue Regeneration Using Dental Pulp Stem Cells Isolated and Expanded in Human Serum

Journal of endodontics, 2017-04, Vol.43 (4), p.568-574

2017

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Ribosomal protein L24 defect in Belly spot and tail (Bst), a mouse Minute

Development (Cambridge), 2004-08, Vol.131 (16), p.3907-3920

2004

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Phenotypic, trophic, and regenerative properties of mesenchymal stem cells from different osseous tissues

Cell and tissue research, 2022-04, Vol.388 (1), p.75-88

2022

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Fusion Between Transcription Factor CBFβ/PEBP2β and a Myosin Heavy Chain in Acute Myeloid Leukemia

Science (American Association for the Advancement of Science), 1993-08, Vol.261 (5124), p.1041-1044

1993

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Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human gamma and epsilon globin genes

Molecular and Cellular Biology, 1992-11, Vol.12 (11), p.4919-4929

1992

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Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in ten subjects determined by direct sequencing of amplified transcripts

The Journal of clinical investigation, 1989-07, Vol.84 (1), p.342-346

1989

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An OmpA-like protein from Acinetobacter spp. stimulates gastrin and interleukin-8 promoters

Infection and immunity, 2000-06, Vol.68 (6), p.3657-3666

2000

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Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency

American journal of human genetics, 1991-05, Vol.48 (5), p.951-958

1991

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ZBP-89, A Krüppel-Type Zinc Finger Protein, Inhibits Cell Proliferation

Biochemical and biophysical research communications, 1997-08, Vol.237 (2), p.230-234

1997

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Human adenine phosphoribosyltransferase: identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme

The Journal of clinical investigation, 1987-11, Vol.80 (5), p.1409-1415

1987

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Nucleotide sequence of the human APRT gene

Nucleic acids research, 1987-11, Vol.15 (21), p.9086-9086

1987

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Human adenine phosphoribosyltransferase deficiency: demonstration of a single mutant allele common to the Japanese

The Journal of clinical investigation, 1988-03, Vol.81 (3), p.945-950

1988

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Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

Nature genetics, 1993-02, Vol.3 (2), p.118-121

1993

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A compound nucleotide repeat in the neurofibromatosis (NF1) gene

Human molecular genetics, 1993-07, Vol.2 (7), p.1083-1083

1993

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Distribucijske greške u procesu procjene performansi zaposlenih/Distribution errors in the employee performance evaluation process

Vojnotehnički glasnik, 2014-10, Vol.62 (4), p.141-154

2014

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The human ZBP-89 homolog, located at chromosome 3q21, represses gastrin gene expression

Mammalian genome, 1998-02, Vol.9 (2), p.165-167

1998

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DNA Sequences in the Promoter Region of the NF1 Gene Are Highly Conserved between Human and Mouse

Genomics (San Diego, Calif.), 1994-06, Vol.21 (3), p.649-652

1994

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Stem Cell Therapy for Craniofacial Bone Regeneration: A Randomized, Controlled Feasibility Trial

Isolated bilateral macrostomia: literature review and case report

Standardization and Safety of Alveolar Bone–derived Stem Cell Isolation

Stem cells derived from tooth periodontal ligament enhance functional angiogenesis by endothelial cells

Tooth Storage, Dental Pulp Stem Cell Isolation, and Clinical Scale Expansion without Animal Serum

Angiogenic and osteogenic potential of bone repair cells for craniofacial regeneration

Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease

Development of a serum-free system to expand dental-derived stem cells: PDLSCs and SHEDs

Dental Pulp Tissue Regeneration Using Dental Pulp Stem Cells Isolated and Expanded in Human Serum

Ribosomal protein L24 defect in Belly spot and tail (Bst), a mouse Minute

Phenotypic, trophic, and regenerative properties of mesenchymal stem cells from different osseous tissues

Fusion Between Transcription Factor CBFβ/PEBP2β and a Myosin Heavy Chain in Acute Myeloid Leukemia

Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human gamma and epsilon globin genes

Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in ten subjects determined by direct sequencing of amplified transcripts

An OmpA-like protein from Acinetobacter spp. stimulates gastrin and interleukin-8 promoters

Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency

ZBP-89, A Krüppel-Type Zinc Finger Protein, Inhibits Cell Proliferation

Human adenine phosphoribosyltransferase: identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme

Nucleotide sequence of the human APRT gene

Human adenine phosphoribosyltransferase deficiency: demonstration of a single mutant allele common to the Japanese

Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell lines

A compound nucleotide repeat in the neurofibromatosis (NF1) gene

Distribucijske greške u procesu procjene performansi zaposlenih/Distribution errors in the employee performance evaluation process

The human ZBP-89 homolog, located at chromosome 3q21, represses gastrin gene expression

DNA Sequences in the Promoter Region of the NF1 Gene Are Highly Conserved between Human and Mouse

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