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The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis

American journal of human genetics, 2011-05, Vol.88 (5), p.523-535

2011

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P1485: PKM AND PKR EXPRESSION DURING HEMATOPOIESIS AND ERYTHROPOIESIS

HemaSphere, 2023-08, Vol.7 (S3), p.e14234db-n/a

2023

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Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO

Science (American Association for the Advancement of Science), 2013-03, Vol.339 (6123), p.1077-1080

2013

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Membrane-bound Dickkopf-1 in Foxp3+ regulatory T cells suppresses T cell-mediated autoimmune colitis

The Journal of immunology (1950), 2017-05, Vol.198 (1_Supplement), p.156-156.8

2017

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Membrane‐bound Dickkopf‐1 in Foxp3+ regulatory T cells suppresses T‐cell‐mediated autoimmune colitis

Immunology, 2017-10, Vol.152 (2), p.265-275

2017

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Recessive LAMC3 mutations cause malformations of occipital cortical development

Nature genetics, 2011-06, Vol.43 (6), p.590-594

2011

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Spondyloepimetaphyseal dysplasia Pakistani type: Expansion of the phenotype

American journal of medical genetics. Part A, 2013-06, Vol.161A (6), p.1300-1308

2013

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Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.27

2017

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Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (CACP) syndrome

Molecular genetics & genomic medicine, 2018-03, Vol.6 (2), p.230-248

2018

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Retrospective evaluation of patients with organizing pneumonia: is cryptogenic organizing pneumonia different from secondary organizing pneumonia?

Tüberküloz ve toraks, 2017-03, Vol.65 (1), p.1-8

2017

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Gene–disease relationship discovery based on model-driven data integration and database view definition

Bioinformatics, 2009-01, Vol.25 (2), p.230-236

2009

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Investigation of low-dose ritonavir on human peripheral blood mononuclear cells using gene expression whole genome microarrays

Genomics (San Diego, Calif.), 2010-07, Vol.96 (1), p.57-65

2010

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Gene Expression Signature in Peripheral Blood Cells Detects Intracranial Aneurysm

Neurosurgery, 2010-08, Vol.67 (2), p.540-540

2010

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Deleterious mutations in exon 1 of MECP2 in Rett syndrome

European journal of medical genetics, 2006-07, Vol.49 (4), p.313-322

2006

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Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (1), p.27

2017

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Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up

Rheumatology international, 2014-11, Vol.34 (11), p.1539-1544

2014

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Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type: longitudinal observation of radiographic findings in a child heterozygous for a KIF22 mutation

Pediatric Radiology, 2015-04, Vol.45 (5), p.771-776

2015

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Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH

European journal of medical genetics, 2007-09, Vol.50 (5), p.386-391

2007

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Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence?

American journal of medical genetics. Part A, 2016-05, Vol.170A (5), p.1187-1195

2016

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Self-esteem in Turkish diabetic children

Journal of pediatric nursing, 2002-08, Vol.17 (4), p.279-282

2002

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Comparison of antioxidant capacity of cow and ewe milk kefirs

Journal of dairy science, 2018-05, Vol.101 (5), p.3788-3798

2018

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Application of oil‐in‐water nanoemulsions based on grape and cinnamon essential oils for shelf‐life extension of chilled flathead mullet fillets

Journal of the science of food and agriculture, 2022-01, Vol.102 (1), p.105-112

2022

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Gamma Irradiation and the Radiation Shielding Characteristics: For the Lead Oxide Doped the Crosslinked Polystyrene-b-Polyethyleneglycol Block Copolymers and the Polystyrene-b-Polyethyleneglycol-Boron Nitride Nanocomposites

Polymers, 2021-09, Vol.13 (19), p.3246

2021

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A novel neutrosophic AHP-Copeland approach for distance education: towards sustainability

Interactive learning environments, 2022-11, Vol.ahead-of-print (ahead-of-print), p.1-23

2022

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Evaluation of Exudative Pleural Effusions: A Multicenter, Prospective, Observational Study

The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis

P1485: PKM AND PKR EXPRESSION DURING HEMATOPOIESIS AND ERYTHROPOIESIS

Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO

Membrane-bound Dickkopf-1 in Foxp3+ regulatory T cells suppresses T cell-mediated autoimmune colitis

Membrane‐bound Dickkopf‐1 in Foxp3+ regulatory T cells suppresses T‐cell‐mediated autoimmune colitis

Recessive LAMC3 mutations cause malformations of occipital cortical development

Spondyloepimetaphyseal dysplasia Pakistani type: Expansion of the phenotype

Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation

Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (CACP) syndrome

Retrospective evaluation of patients with organizing pneumonia: is cryptogenic organizing pneumonia different from secondary organizing pneumonia?

Gene–disease relationship discovery based on model-driven data integration and database view definition

Investigation of low-dose ritonavir on human peripheral blood mononuclear cells using gene expression whole genome microarrays

Gene Expression Signature in Peripheral Blood Cells Detects Intracranial Aneurysm

Deleterious mutations in exon 1 of MECP2 in Rett syndrome

Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation

Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up

Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type: longitudinal observation of radiographic findings in a child heterozygous for a KIF22 mutation

Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH

Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence?

Self-esteem in Turkish diabetic children

Comparison of antioxidant capacity of cow and ewe milk kefirs

Application of oil‐in‐water nanoemulsions based on grape and cinnamon essential oils for shelf‐life extension of chilled flathead mullet fillets

Gamma Irradiation and the Radiation Shielding Characteristics: For the Lead Oxide Doped the Crosslinked Polystyrene-b-Polyethyleneglycol Block Copolymers and the Polystyrene-b-Polyethyleneglycol-Boron Nitride Nanocomposites

A novel neutrosophic AHP-Copeland approach for distance education: towards sustainability

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