Lista de obras - James C Barton - Dominio Público Uruguay

15-Hydroxyprostaglandin dehydrogenase and delta 13 reductase content of gastrointestinal organs of rabbits and rats

artículo científico publicado en 1981

A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.

artículo científico publicado en 2011

A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study.

artículo científico publicado en 2007

Abnormalities of flavin monooxygenase as an etiology for sideroblastic anemia

scientific article published on 01 October 2000

Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening study.

artículo científico publicado en 2008

Active transport of lead-210 by everted segments of rat duodenum

artículo científico publicado en 1984

Acute lymphoblastic leukemia in idiopathic refractory sideroblastic anemia: evidence for a common lymphoid and myeloid progenitor cell

scientific article published on 01 January 1980

African Americans at risk for increased iron stores or liver disease

artículo científico publicado en 2007

Analysis of paraprotein transport into the saliva by using anti-idiotype antibodies

scientific article published on 01 January 1987

Anemia and iron kinetics in alcoholism.

artículo científico publicado en 1980

Assessment of total immunoreactive lactoferrin in hematopoietic cells using flow cytometry

scientific article published on 01 April 1988

Beneficial Effects of Hepatitis in Patients with Acute Myelogenous Leukemia

artículo científico publicado el 1 de febrero de 1979

Bilateral subdural hematomas in an adult with hereditary factor VII deficiency: A complication of sit-ups and inversion?

scientific article published on 26 December 2007

Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

artículo científico publicado en 2007

Blood lead concentrations in hereditary hemochromatosis.

artículo científico publicado en 1994

Bone metastases in malignant gastrinoma

scientific article published on 01 November 1986

Calcium inhibition of inorganic iron absorption in rats

scientific article published on 01 January 1983

Characterization of adult patients with IgG subclass deficiency and subnormal IgG2

artículo científico publicado en 2020

Chelation therapy for iron overload.

artículo científico publicado en 2007

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes.

artículo científico publicado en 2018

Clinical and laboratory associations of mannose-binding lectin in 219 adults with IgG subclass deficiency

scientific article published on 22 May 2019

Clinical approach to pancytopenia

artículo científico publicado el 1 de julio de 1981

Clinical guidelines: HFE hemochromatosis-screening, diagnosis and management

artículo científico publicado en 2010

Coagulation testing of Hickman catheter blood in patients with acute leukemia

scientific article published on 01 November 1986

Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome

artículo científico publicado en 1998

Comparison of the unsaturated iron-binding capacity with transferrin saturation as a screening test to detect C282Y homozygotes for hemochromatosis in 101,168 participants in the hemochromatosis and iron overload screening (HEIRS) study

artículo científico publicado en 2005

Concerns in a primary care population about genetic discrimination by insurers.

artículo científico publicado en 2005

Current status of blastic transformation in chronic myelogenous leukemia ⬇️

artículo científico publicado el 1 de enero de 1978

Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study.

artículo científico publicado en 2007

Diabetes in HFE Hemochromatosis.

artículo científico publicado en 2017

Diagnosis of hemochromatosis in family members of probands: a comparison of phenotyping and HFE genotyping

scientific article published on 01 March 1999

Drug evaluation: Deferitrin for iron overload disorders

artículo científico publicado en 2007

Drug evaluation: deferitrin (GT-56-252; NaHBED) for iron overload disorders.

artículo científico publicado en 2007

Duration of frequent or severe respiratory tract infection in adults before diagnosis of IgG subclass deficiency.

artículo científico publicado en 2019

Early age-of-onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A-->T) in an African American male of West Indies descent

scientific article published on 19 May 2008

Effect of iron deficiency on bleomycin-induced lung fibrosis in the hamster

artículo científico publicado en 1988

Effect of phosphate on the absorption and retention of lead in the rat

artículo científico publicado en 1981

Effects of calcium on the absorption and retention of lead

artículo científico publicado el 1 de marzo de 1978

Effects of ethanol on the absorption and retention of lead

artículo científico publicado en 1978

Effects of iron on the absorption and retention of lead

artículo científico publicado en 1978

Effects of vitamin D on the absorption and retention of lead

scientific article published on 01 February 1980

Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload.

artículo científico publicado en 2015

Factors affecting iron balance.

artículo científico publicado en 1981

Factors affecting the absorption and excretion of lead in the rat ⬇️

artículo científico publicado el 1 de abril de 1978

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans

artículo científico publicado en 2003

GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.

artículo científico publicado en 2016

Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin.

artículo científico publicado en 2004

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

artículo científico publicado en 1997

Genotypic and phenotypic heterogeneity of African Americans with primary iron overload

artículo científico publicado en 2003

HAMP promoter mutation nc.-153C>T in 785 HEIRS study participants.

artículo científico publicado en 2009

HFE C282Y and H63D in adults with malignancies in a community medical oncology practice

artículo científico publicado en 2004

HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study

artículo científico publicado en 2009

HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening

scientific article published on 01 January 2007

HFE gene: Structure, function, mutations, and associated iron abnormalities.

artículo científico publicado en 2015

HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.

artículo científico publicado en 2001

HFE hemochromatosis and hepatic sarcoid

artículo científico publicado en 2009

HFE mutations in African-American women with non-insulin-dependent diabetes mellitus.

artículo científico publicado en 2001

HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L

artículo científico publicado en 2013

HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants

artículo científico publicado en 2009

HLA-A and -B Type and Haplotype Frequencies in IgG Subclass Deficiency Subgroups

scientific article published on 20 April 2020

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.

artículo científico publicado en 2002

Haemochromatosis

artículo científico publicado en 2007

Heme carrier protein 1 (HCP1) genetic variants in the Hemochromatosis and Iron Overload Screening (HEIRS) Study participants

artículo científico publicado en 2009

Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults

artículo científico publicado en 2003

Hemochromatosis and Vibrio vulnificus wound infections.

artículo científico publicado en 2009

Hemochromatosis and iron overload: from bench to clinic.

artículo científico publicado en 2013

Hemochromatosis and iron therapy of Restless Legs Syndrome.

artículo científico publicado en 2001

Hemochromatosis and iron-overload screening in a racially diverse population.

artículo científico publicado en 2005

Hemochromatosis detection in a health screening program at an Alabama forest products mill.

artículo científico publicado en 2002

Hemochromatosis in a Lithuanian with HFE C282Y homozygosity and C282Y allele frequencies in the Baltic Sea region

artículo científico publicado en 2001

Hemochromatosis, HFE C282Y homozygosity, and bariatric surgery: report of three cases

artículo científico publicado en 2004

Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis.

artículo científico publicado en 2004

Hepatitis and leukemia

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study

artículo científico publicado en 2010

How I treat hemochromatosis.

scientific article published on 22 March 2010

Hypogonadotrophic hypogonadism due to intrasellar hemangioblastoma in von Hippel-Lindau syndrome

artículo científico publicado en 2009

Immune deficiency and expanded population of granular lymphocytes after bone marrow transplantation

artículo científico publicado en 1987

Immune thrombocytopenia: effects of maternal gamma globulin infusion on maternal and fetal serum, platelet, and monocyte IgG.

artículo científico publicado en 1987

Immunoreactive lactoferrin in resting, activated, and neoplastic lymphocytes

artículo científico publicado en 1990

Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency.

artículo científico publicado en 2001

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening Study

artículo científico publicado en 2006

Intravenous Bevacizumab Therapy in a Patient with Hereditary Hemorrhagic Telangiectasia, ENG E137K, Alcoholic Cirrhosis, and Portal Hypertension.

artículo científico publicado en 2017

Iron deficiency due to excessive therapeutic phlebotomy in hemochromatosis

scientific article published on 01 November 2000

Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases

scientific article published on 01 October 2006

Iron overload in African Americans

artículo científico publicado en 1995

Iron overload in an African American woman with SS hemoglobinopathy and a promoter mutation in the X-linked erythroid-specific 5-aminolevulinate synthase (ALAS2) gene.

artículo científico publicado en 2005

Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y

artículo científico publicado en 2022

Iron, lead, and cobalt absorption: similarities an dissimilarities

scientific article published on 01 January 1981

Iron-binding reactivity in mature neutrophils: relative cell content quantification by cytochemical scoring

artículo científico publicado en 1988

Isolated chylopericardium associated with lymphoma

scientific article published on 01 November 1980

Juvenile hemochromatosis in the southeastern United States: a report of seven cases in two kinships

artículo científico publicado en 2002

Listeria monocytogenes Infection in Hairy Cell Leukemia: A Case Report and Literature Review.

artículo científico publicado en 2018

Liver diseases in the hemochromatosis and iron overload screening study.

artículo científico publicado en 2006

Management of Hemochromatosis

artículo científico publicado en 1998

Management of hemochromatosis in a Jehovah's Witness

scientific article published on 01 January 2005

Mixture models of serum iron measures in population screening for hemochromatosis and iron overload.

artículo científico publicado en 2006

Neutrophil function in chronic neutrophilic leukemia: defective respiratory burst in response to phorbol esters

artículo científico publicado en 1992

Neutrophil lactoferrin content: variation among mammals

artículo científico publicado en 1988

Nonhemolytic, noninfectious transfusion reactions.

artículo científico publicado en 1981

Normal transferrin saturation in hemochromatosis

scientific article published on 01 April 1991

Optimal management strategies for chronic iron overload.

artículo científico publicado en 2007

Patient compliance with phlebotomy therapy for iron overload associated with hemochromatosis

artículo científico publicado en 2003

Peripheral blood erythrocyte parameters in hemochromatosis: evidence for increased erythrocyte hemoglobin content

scientific article published on 01 January 2000

Phlebotomy-mobilized iron as a surrogate for liver iron content in hemochromatosis patients.

artículo científico publicado en 2003

Population screening for hemochromatosis: has the time finally come?

artículo científico publicado en 2000

Porphyria cutanea tarda associated with HFE C282Y homozygosity, iron overload, and use of a contraceptive vaginal ring

artículo científico publicado en 2016

Preleukemia in Fanconi's anemia: hematopoietic cell multinuclearity, membrane duplication, and dysgranulogenesis

artículo científico publicado en 1987

Prevalence of iron deficiency in 62,685 women of seven race/ethnicity groups: The HEIRS Study

artículo científico publicado en 2020

Probability of C282Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the hemochromatosis and iron overload screening study ⬇️

artículo científico publicado el 18 de abril de 2012

Provoked priapism in sickle cell anemia

artículo científico publicado en 1980

Pseudochloroma: Extramedullar Hematopoietic Nodules in Chronic Myelogenous Leukemia

artículo científico publicado el 1 de noviembre de 1979

Psychosocial impact of genetic testing for hemochromatosis in the HEIRS Study: a comparison of participants recruited in Canada and in the United States.

artículo científico publicado en 2007

Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study

artículo científico publicado en 2006

Relationships of serum free thyroxine and erythrocyte measures in euthyroid HFE C282Y homozygotes and control subjects: the HEIRS study.

artículo científico publicado en 2009

Remission of porphyria cutanea tarda after anastrozole treatment of breast cancer.

artículo científico publicado en 2007

Reply

artículo científico publicado en 2017

Reply

artículo científico publicado en 2015

Reply

scientific article published on 15 March 2016

Reply: To PMID 25605615.

artículo científico publicado en 2015

Rheumatoid arthritis associated with expanded populations of granular lymphocytes.

artículo científico publicado en 1986

SLC40A1 c.1402G-->a results in aberrant splicing, ferroportin truncation after glycine 330, and an autosomal dominant hemochromatosis phenotype.

artículo científico publicado en 2007

Screening for hemochromatosis in routine medical care: an evaluation of mean corpuscular volume and mean corpuscular hemoglobin

scientific article published on 01 January 2000

Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study

artículo científico publicado en 2009

Serum Ferritin Level Predicts Advanced Hepatic Fibrosis among U.S. Patients with Phenotypic Hemochromatosis

artículo científico publicado el 15 de abril de 2003

Serum ferritin and transferrin saturation in Asians and Pacific Islanders

scientific article published on 01 April 2007

Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary-care population

artículo científico publicado en 2008

Serum ferritin is a biomarker for liver mortality in the Hemochromatosis and Iron Overload Screening Study

artículo científico publicado en 2015

Severity of iron overload in hemochromatosis: effect of volunteer blood donation before diagnosis

artículo científico publicado en 2001

Should we treat individuals homozygous for HFE p.Cys282Tyr with ferritin 300-1000 μg/L?

artículo científico publicado en 2017

Sideroblastic anemia, iron overload, and ALAS2 R452S in African-American males: phenotype and genotype features of five unrelated patients.

artículo científico publicado en 2011

Stainable hepatic iron in 341 African American adults at coroner/medical examiner autopsy

artículo científico publicado en 2005

Survey of physician knowledge about hemochromatosis

artículo científico publicado en 2002

The aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome

artículo científico publicado en 1979

The mitochondrial nt 16189 polymorphism and hereditary hemochromatosis

scientific article published on 01 November 2004

Three kinships with ALAS2 P520L (c. 1559 C --> T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload.

artículo científico publicado en 2006

Thrombotic thrombocytopenic purpura in systemic sclerosis

artículo científico publicado en 1989

Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama

artículo científico publicado en 2000

Transfusion iron overload in adults with acute leukemia: manifestations and therapy

artículo científico publicado en 2000

Tumor lysis syndrome in nonhematopoietic neoplasms

artículo científico publicado en 1989

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands

scientific article published on 01 June 1999

Ultrastructural cytochemical identification of the siderophilic enterocyte

scientific article published on 01 July 1984

Ultrastructural cytochemistry and radioautography of hemoglobin--iron absorption

scientific article published on 01 April 1981

Ultrastructural cytochemistry of iron absorption ⬇️

artículo científico publicado el 1 de diciembre de 1978

Ultrastructural localization of transferrin, transferrin receptor, and iron-binding sites on human placental and duodenal microvilli

scientific article published on 01 May 1985

Ultrastructural morphology and cytochemistry of iron-deficient polymorphonuclear leukocytes

artículo científico publicado en 1986

Ultrastructural silver enhancement of Prussian blue-reactive iron in hematopoietic and intestinal cells.

artículo científico publicado en 1988

Vibrio vulnificus bacteremia associated with chronic lymphocytic leukemia, hypogammaglobulinemia, and hepatic cirrhosis: relation to host and exposure factors in 252 V. vulnificus infections reported in Louisiana

artículo científico publicado en 2006

Vibrio vulnificus infection in a hemodialysis patient receiving intravenous iron therapy.

artículo científico publicado en 2003

Lista de obras de James C Barton

15-Hydroxyprostaglandin dehydrogenase and delta 13 reductase content of gastrointestinal organs of rabbits and rats

A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.

A genome-wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study.

Abnormalities of flavin monooxygenase as an etiology for sideroblastic anemia

Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening study.

Active transport of lead-210 by everted segments of rat duodenum

Acute lymphoblastic leukemia in idiopathic refractory sideroblastic anemia: evidence for a common lymphoid and myeloid progenitor cell

African Americans at risk for increased iron stores or liver disease

Analysis of paraprotein transport into the saliva by using anti-idiotype antibodies

Anemia and iron kinetics in alcoholism.

Assessment of total immunoreactive lactoferrin in hematopoietic cells using flow cytometry

Beneficial Effects of Hepatitis in Patients with Acute Myelogenous Leukemia

Bilateral subdural hematomas in an adult with hereditary factor VII deficiency: A complication of sit-ups and inversion?

Bivariate mixture modeling of transferrin saturation and serum ferritin concentration in Asians, African Americans, Hispanics, and whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Blood lead concentrations in hereditary hemochromatosis.

Bone metastases in malignant gastrinoma

Calcium inhibition of inorganic iron absorption in rats

Characterization of adult patients with IgG subclass deficiency and subnormal IgG2

Chelation therapy for iron overload.

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes.

Clinical and laboratory associations of mannose-binding lectin in 219 adults with IgG subclass deficiency

Clinical approach to pancytopenia

Clinical guidelines: HFE hemochromatosis-screening, diagnosis and management

Coagulation testing of Hickman catheter blood in patients with acute leukemia

Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome

Comparison of the unsaturated iron-binding capacity with transferrin saturation as a screening test to detect C282Y homozygotes for hemochromatosis in 101,168 participants in the hemochromatosis and iron overload screening (HEIRS) study

Concerns in a primary care population about genetic discrimination by insurers.

Current status of blastic transformation in chronic myelogenous leukemia ⬇️

Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study.

Diabetes in HFE Hemochromatosis.

Diagnosis of hemochromatosis in family members of probands: a comparison of phenotyping and HFE genotyping

Drug evaluation: Deferitrin for iron overload disorders

Drug evaluation: deferitrin (GT-56-252; NaHBED) for iron overload disorders.

Duration of frequent or severe respiratory tract infection in adults before diagnosis of IgG subclass deficiency.

Early age-of-onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A-->T) in an African American male of West Indies descent

Effect of iron deficiency on bleomycin-induced lung fibrosis in the hamster

Effect of phosphate on the absorption and retention of lead in the rat

Effects of calcium on the absorption and retention of lead

Effects of ethanol on the absorption and retention of lead

Effects of iron on the absorption and retention of lead

Effects of vitamin D on the absorption and retention of lead

Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload.

Factors affecting iron balance.

Factors affecting the absorption and excretion of lead in the rat ⬇️

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans

GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.

Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin.

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

Genotypic and phenotypic heterogeneity of African Americans with primary iron overload

HAMP promoter mutation nc.-153C>T in 785 HEIRS study participants.

HFE C282Y and H63D in adults with malignancies in a community medical oncology practice

HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study

HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening

HFE gene: Structure, function, mutations, and associated iron abnormalities.

HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.

HFE hemochromatosis and hepatic sarcoid

HFE mutations in African-American women with non-insulin-dependent diabetes mellitus.

HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L

HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants

HLA-A and -B Type and Haplotype Frequencies in IgG Subclass Deficiency Subgroups

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.

Haemochromatosis

Heme carrier protein 1 (HCP1) genetic variants in the Hemochromatosis and Iron Overload Screening (HEIRS) Study participants

Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults

Hemochromatosis and Vibrio vulnificus wound infections.

Hemochromatosis and iron overload: from bench to clinic.

Hemochromatosis and iron therapy of Restless Legs Syndrome.

Hemochromatosis and iron-overload screening in a racially diverse population.

Hemochromatosis detection in a health screening program at an Alabama forest products mill.

Hemochromatosis in a Lithuanian with HFE C282Y homozygosity and C282Y allele frequencies in the Baltic Sea region

Hemochromatosis, HFE C282Y homozygosity, and bariatric surgery: report of three cases

Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis.

Hepatitis and leukemia

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study

How I treat hemochromatosis.

Hypogonadotrophic hypogonadism due to intrasellar hemangioblastoma in von Hippel-Lindau syndrome

Immune deficiency and expanded population of granular lymphocytes after bone marrow transplantation

Immune thrombocytopenia: effects of maternal gamma globulin infusion on maternal and fetal serum, platelet, and monocyte IgG.

Immunoreactive lactoferrin in resting, activated, and neoplastic lymphocytes