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Hereditary hemochromatosis: An opportunity for gene therapy
Hereditary breast cancer: new genetic developments, new therapeutic avenues
Hereditary hypophosphatemias: New genes in the bone-kidney axis
Heregulin Regulates Prolactinoma Gene Expression
Heregulin-induced activation of ErbB3 by EGFR tyrosine kinase activity promotes tumor growth and metastasis in melanoma cells
Hereditary haemochromatosis mutation frequencies in the general population
Hereditary canine spinal muscular atrophy is phenotypically similar but molecularly distinct from human spinal muscular atrophy
Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients
Hereditary Breast Cancer: Practical Pursuit for Clinical Translation
Hereditary breast and ovarian cancers
Hereditary Kidney Cancer Unique Opportunity for Disease-based Therapy
Hereditary breast cancer
Hereditary breast cancer: Part I. Diagnosing hereditary breast cancer syndromes
Heredity in epilepsy: Neurodevelopment, comorbidity, and the neurological trait
Hereditary predispositions to cancer: The genetic diagnosis in practice.
Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrin
Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter Study
Hereditary cancer syndromes
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations
Hereditary determinants of human hypertension - Strategies in the setting of genetic complexity
Hereditary Pituitary Hyperplasia with Infantile Gigantism
Hereditary hormone excess: Genes, molecular pathways, and syndromes
Hereditary hemochromatosis: Generation of a transcription map within a refined and extended map of the HLA class I region
Hereditary barrier-related diseases involving the tight junction: lessons from skin and intestine
Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms
Here is the evidence, now what is the hypothesis? The complementary roles of inductive and hypothesis-driven science in the post-genomic era
Hereditary sensory and autonomic neuropathy type II A: Early neurological and skeletal findings
Here is diabetes in The Lancet's tuberculosis Series!
Hereditary nonpolyposis colorectal cancer in Pakistan: Results of a pilot study
Hereditary diffuse gastric cancer: A manifestation of lost cell polarity
Hereditary recurrent fever syndromes (HRF). A subgroup of autoinflammatory diseases (AID)
Hereditary Colon Cancer Syndromes
Hereditary Cancer-associated Missense Mutations in hMSH6 Uncouple ATP Hydrolysis from DNA Mismatch Binding
Hereditary iron overload
Hereditary lysozyme amyloidosis - phenotypic heterogeneity and the role of solid organ transplantation
Hereditary colorectal cancer: MYH-associated polyposis and other newly identified disorders
Hereditary Disorders Presenting with Urticaria
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
Hereditary bone tumors
Hereditary Cancer-Associated Mutations in Women Diagnosed with Two Primary Cancers: An Opportunity to Identify Hereditary Cancer Syndromes after the First Cancer Diagnosis
Hereditary breast and ovarian cancer syndrome: Considering the complexities
Hereditary and Histologic Characteristics of the CF1/b cac Mouse Cataract Model
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation
Hereditary Cancer Risk Assessment in a Pediatric Oncology Follow-Up Clinic
Hereditary Hemochromatosis: A Literature Review and Case Report
Hereditary hemochromatosis and diabetes mellitus: implications for clinical practice
Hereditary spastic paraplegia with thin corpus callosum
Hereditary colorectal cancer
Hereditary Gynecologic Cancers Risk Assessment, Counseling, Testing and Management
Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia - SPG11, SPG15, and further genetic heterogeneity
Hereditary spastic paraplegias: an update
Heredity of Restless Legs Syndrome in a Pregnant Population
Hereditary thrombophilias and stroke
Hereditary haemochromatosis
Hereditary hemorrhagic telangiectasia patients can tolerate anticoagulation
Hereditary pulmonary alveolar proteinosis caused by recessive CSF2RB mutations
Hereditary Hemochromatosis: Pathogenesis, Diagnosis, and Treatment
Hereditary breast cancer: from molecular pathology to tailored therapies