465 results on '"Alzahrani, Ali S."'
Search Results
52. LncRNA GAS8-AS1dinucleotide genetic variantn.713A>G, n.714T>Cis associated with early-stage disease, lymph node, and distant metastasis in differentiated thyroid cancer
53. A Single Schottky Barrier MOSFET-Based Leaky Integrate and Fire Neuron for Neuromorphic Computing
54. How do BRAFV600E and TERT promoter mutations interact with the ATA and TNM staging systems in thyroid cancer?
55. LBMON173 Non-functioning Seller Masses: Tumor Types, Surgical Management And Course Over Time
56. Neural-based fixed-time attitude tracking control for space vehicle subject to constrained outputs
57. Editorial overview: Genetics of endocrine tumors
58. A CYP11A1 homozygous exonic variant inducing an alternative splicing, frameshift and truncation in a family with congenital adrenal hyperplasia
59. β-catenin attenuation leads to up-regulation of activating NKG2D ligands and tumor regression in BrafV600E-driven thyroid cancer cells.
60. Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant
61. TERT Promoter Mutations in Thyroid Cancer
62. A Unique Mechanism of a Novel SynonymousPHEXVariant Causing X-Linked Hypophosphatemia
63. Gliomas: Genetic alterations, mechanisms of metastasis, recurrence, drug resistance, and recent trends in molecular therapeutic options
64. Fumarate Hydratase is a Novel Gene for Familial Non-Medullary Thyroid Cancer
65. Papillary Thyroid Cancer and a TERT Promotor Mutation-positive Paraganglioma in a Patient With a Germline SDHB Mutation
66. Gliomas: Genetic alterations, mechanisms of metastasis, recurrence, drug resistance, and recent trends in molecular therapeutic options
67. Effect of TiO2 on the sinter crystallization of nepheline glasses for dental application
68. Indirect-Neural-Approximation-Based Fault-Tolerant Integrated Attitude and Position Control of Spacecraft Proximity Operations
69. A new neural network-based optimal mixed H2/H∞ control for a modified unmanned aerial vehicle subject to control input constraints
70. SARS-CoV-2: Emerging Role in the Pathogenesis of Various Thyroid Diseases
71. A Novel Mutation in a Gene Causes Sclerosteosis in a Family of Mediterranean Origin
72. A Review of Glass and Crystallizations of Glass-Ceramics
73. COVID-19-Related Pulmonary Embolism: Incidence, Characteristics, and Risk Factors
74. Comparison of differentiated thyroid cancer in children and adolescents (≤20 years) with young adults
75. Controversy on the management of patients carrying RET p.V804M mutation
76. Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism
77. Mutation of SGK3, a novel regulator of renal phosphate transport, causes autosomal dominant hypophosphatemic Rickets
78. A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked Hypophosphatemia.
79. β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model
80. A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population
81. Mutation prediction by PolyPhen or functional assay, a detailed comparison of CYP27B1 missense mutations
82. Outcome of gonadotropin therapy for male infertility due to hypogonadotrophic hypogonadism
83. THE POTENTIAL ROLE OF THE SODIUM SYMPORTER GENE POLYMORPHISM IN THE DEVELOPMENT OF DIFFERENTIATED THYROID CANCER: 808
84. Increased CYP24A1 expression is associated with BRAFV600E mutation and advanced stages in papillary thyroid carcinoma
85. The diagnostic value of fused positron emission tomography/computed tomography in the localization of adrenocorticotropin-secreting pituitary adenoma in Cushing’s disease
86. Molecular genetics of disorders of sex development in a highly consanguineous population
87. Single nucleotide polymorphisms in matrix metalloproteinase 2 (MMP2) enhance BRAFV600E mutation-mediated oncogenicity and invasiveness of papillary thyroid cancer cells
88. Repeated Remissions of Cushing's Disease Due to Recurrent Infarctions of an ACTH-Producing Pituitary Macroadenoma
89. High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines
90. Preoperative Neck Ultrasonographic Mapping for Persistent/Recurrent Papillary Thyroid Cancer
91. Natural Course of the American Thyroid Association Response to Therapy Statuses (Dynamic Risk Stratification) in Differentiated Thyroid Cancer
92. Molecular Analysis of CYP27B1 Mutations in Vitamin D-Dependent Rickets Type 1A: c.590G > A (p.G197D) Missense Mutation Causes a RNA Splicing Error
93. Course and Predictive Factors of Incomplete Response to Therapy in Low- and Intermediate-Risk Thyroid Cancer
94. Association Between BRAF V600E Mutation and Mortality in Patients With Papillary Thyroid Cancer
95. A Unique Mechanism of a Novel Synonymous PHEXVariant Causing X-Linked Hypophosphatemia
96. An Acceptor Site Mutation in Intron 1 of the Steroid 5α-Reductase-2 (SRD5A2) Gene in Two Unrelated Cases of 46XY Male Pseudohermaphordite.
97. A Novel Biallelic Mutation in the Insulin Binding Domain of the Insulin Receptor Causing Severe Insulin Resistance Syndrome in Five Unrelated Saudi Families; a Possible Founder Mutation.
98. Radioactive Iodine (I-131) Therapy for Thyroglobulin Positive, Scan Negative Differentiated Thyroid Cancer.
99. Long-Term Outcome of Patients with Persistent Differentiated Thyroid Cancer Following the Initial Management.
100. Insights of Noncanonical Splice-site Variants on RNA Splicing in Patients With Congenital Hypothyroidism.
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