J. Kant

发表

The Histopathology of PRSS1 Hereditary Pancreatitis

R. Pai, D. Yadav, R. Brand, 2014, The American journal of surgical pathology.

Clinical laboratory reports in molecular pathology.

M. Gulley, R. Braziel, S. Ogino, 2007, Archives of pathology & laboratory medicine.

Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology.

Tina Hambuch, Lisa Kalman, Rong Mao, 2012, The Journal of molecular diagnostics : JMD.

Next generation sequencing in clinical medicine: Challenges and lessons for pathology and biomedical informatics

Michael J. Becich, Lucas Santana-Santos, Rama R. Gullapalli, 2012, Journal of pathology informatics.

Oriinal articles Paternal transmission ofcongenital myotonic dystrophy

E. Zackai, J. Kant, 1994 .

Effect of chronic denervation and denervation-reinnervation on cytoplasmic creatine kinase transcript accumulation.

Simon C Watkins, J. Watchko, J. Kant, 2001, Journal of neurobiology.

Reproductive factors and ovarian cancer risk in Jewish BRCA1 and BRCA2 mutation carriers (United States)

D. Fishman, B. Karlan, D. Cramer, 2003, Cancer Causes & Control.

Recalcitrance of bacterial vaginosis among herpes‐simplex‐virus‐type‐2‐seropositive women

D. Landsittel, J. Kant, T. Cherpes, 2012, The journal of obstetrics and gynaecology research.

Lymphomas and leukemias in the relatives of patients with mycosis fungoides

M. Greene, J. Kant, H. Pinto, 1982, Cancer.

JAK2 V617F mutation in patients with catastrophic intra-abdominal thromboses.

S. Swerdlow, C. McMahon, J. Kant, 2007, American journal of clinical pathology.

Opportunities and Challenges Associated with Clinical Diagnostic Genome Sequencing

T. Greiner, T. Hambuch, W. Grody, 2019 .

Genital tract shedding of herpes simplex virus type 2 in women: effects of hormonal contraception, bacterial vaginosis, and vaginal group B Streptococcus colonization.

L. Meyn, M. Melan, J. Kant, 2005, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Genetic heterogeneity in hereditary breast cancer: role of BRCA1 and BRCA2.

F. Couch, T. Rebbeck, B. Weber, 1996, American journal of human genetics.

Phase II Trial of Short-Course CHOP-R Followed by 90Y-ibritumomab Tiuxetan and Extended Rituximab in Previously Untreated Follicular Lymphoma

S. Swerdlow, K. Foon, S. Land, 2008, Clinical Cancer Research.

10Techniques to Detect Disease and Response to Therapy: Minimal Residual Disease

J. Kant, M. Beckner, 2010 .

Molecular Techniques to Detect Disease and Response to Therapy: Minimal Residual Disease

J. Kant, M. Beckner, 2010 .

Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays.

S. Kash, F. Monzon, S. Lilleberg, 2010, The Journal of molecular diagnostics : JMD.

Hepatosplenic γδ T-cell lymphoma : Ultrastructural, immunophenotypic, and functional evidence for cytotoxic T lymphocyte differentiation

P. Nowell, R. DiPaola, J. Kant, 1997 .

In vivo treatment of human leukemia in a scid mouse model with c-myb antisense oligodeoxynucleotides.

G. Zon, M. Ratajczak, A. Gewirtz, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Retroviral activation of interleukin 2 gene in a gibbon ape T cell lymphoma line

G. Crabtree, N. Holbrook, J. Kant, 1986, The Journal of experimental medicine.

REGULATION AND CHARACTERIZATION OF THE mRNAs FOR THE Aα, Bβ AND γ CHAINS OF FIBRINOGEN

G. Crabtree, A. Fornace, D. Fowlkes, 1983 .

Plaque-Associated Neuronal Proteins: A Recurrent Motif in Neuritic Amyloid Deposits throughout Diverse Cortical Areas of the Alzheimer's Disease Brain

M. L. Schmidt, J. Trojanowski, V. Lee, 1994, Experimental Neurology.

The rat fibrinogen genes. Linkage of the A alpha and gamma chain genes.

G. Crabtree, J. Kant, 1983, The Journal of biological chemistry.

High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing.

W. Linehan, W. Linehan, K. Pacak, 2006, The Journal of clinical endocrinology and metabolism.

The Associations Between Pelvic Inflammatory Disease, Trichomonas vaginalis Infection, and Positive Herpes Simplex Virus Type 2 Serology

L. Meyn, M. Melan, J. Kant, 2006, Sexually transmitted diseases.

Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reaction

E. Rappaport, P. Fortina, S. Surrey, 1992, Human Genetics.

Variability in the Michelin tire syndrome. A child with multiple anomalies, smooth muscle hamartoma, and familial paracentric inversion of chromosome 7q.

E. Zackai, N. Spinner, R. Schnur, 1993, Journal of the American Academy of Dermatology.

Iron binding saturation and genotypic testing for hereditary hemochromatosis in patients with liver disease.

J. Kant, L. Nichols, G. Dickson, 2006, American journal of clinical pathology.

Coincident Kaposi sarcoma and T‐cell lymphoma in a patient with the Wiskott‐Aldrich syndrome

K. Siminovitch, J. Brooks, J. Kant, 1992, American journal of hematology.

Gastric small lymphocytic proliferation with immunoglobulin gene rearrangement in pseudolymphoma versus lymphoma.

J. Brooks, J. Kant, S. Saul, 1989, Gastroenterology.

Secondary Ph-positive CML with a minority monosomy 7 clone.

P. Nowell, J. Glick, J. Kant, 1987, Cancer genetics and cytogenetics.

A tale of two systems: Pathology resident recruitment in and out of the National Resident Matching Program.

J. Kant, 2001, Human pathology.

Hepatitis C Virus Quantitation: Optimization of Strategies for Detecting Low-Level Viremia

J. Kant, K. Weck, W. T. Hofgärtner, 2000, Journal of Clinical Microbiology.

Cutaneous Marginal Zone Lymphomas Have Distinctive Features and Include 2 Subsets

S. Swerdlow, J. Kant, James T. Edinger, 2010, The American journal of surgical pathology.

CD123 Immunohistochemical Expression in Acute Myeloid Leukemia is Associated With Underlying FLT3-ITD and NPM1 Mutations

M. Boyiadzis, K. Warita, J. Kant, 2012, Applied immunohistochemistry & molecular morphology : AIMM.

Absence of t(14;18) major and minor breakpoints and of Bcl-2 protein overproduction in Reed-Sternberg cells of Hodgkin's disease.

John Calvin Reed, D. Louie, J. Brooks, 1991, The American journal of pathology.

Impact of Genomic Sequence Variability on Quantitative PCR Assays for Diagnosis of Polyomavirus BK Infection

J. Kant, P. Randhawa, R. Shapiro, 2011, Journal of Clinical Microbiology.

Clonal analysis of solitary follicular nodules in the thyroid.

J. Puck, V. Livolsi, J. Kant, 1990, The American journal of pathology.

Coordinate accumulation of the mRNAs for the alpha, beta, and gamma chains of rat fibrinogen following defibrination.

G. Crabtree, J. Kant, 1982, The Journal of biological chemistry.

Molecular cloning of cDNA for the alpha, beta, and gamma chains of rat fibrinogen. A family of coordinately regulated genes.

G. Crabtree, J. Kant, 1981, The Journal of biological chemistry.

Two regions within the human IL-2 gene promoter are important for inducible IL-2 expression.

J. Kant, S. Pancer, M. Kamoun, 1988, Journal of immunology.

Rapid diagnosis of herpes simplex encephalitis using microchip electrophoresis of PCR products.

J. Landers, A. Hühmer, J. Kant, 1999, Clinical chemistry.

Direct DNA sequencing in the clinical laboratory.

J. Kant, 1995, Clinical chemistry.

Richter's syndrome associated with loss of response to transforming growth factor-beta.

P. Nowell, F. Fox, J. Kant, 1994, Leukemia research.

Partial mRNA sequences for human Aa , Bf 3 , and y fibrinogen chains : Evolutionary and functional implications ( multigene families / cDNA

G. Crabtree, S. Lord, J. Kant, 2022 .

Myeloperoxidase-positive acute megakaryoblastic leukemia.

L. Moscinski, J. Kant, M. Prystowsky, 1989, American journal of clinical pathology.

Biologic diversity of polyomavirus BK genomic sequences: Implications for molecular diagnostic laboratories

J. Kant, P. Randhawa, M. Bueno, 2008, Journal of medical virology.

Marrow fibrosis associated with a Philadelphia chromosome.

P. Nowell, J. Kant, J. Finan, 1992, Cancer genetics and cytogenetics.

Clonal T-cell receptor β-chain gene rearrangements in differential diagnosis of lymphomatoid papulosis from skin metastasis of nodal anaplastic large-cell lymphoma.

O. Akilov, J. Kant, L. Grandinetti, 2011, Archives of dermatology.

Epigenetic abnormality of SRY gene in the adult XY female with pericentric inversion of the Y chromosome

Y. Tabuchi, I. Takasaki, T. Kondo, 2010, Congenital anomalies.

Genotyping Schemes for Polyomavirus BK, Using Gene-Specific Phylogenetic Trees and Single Nucleotide Polymorphism Analysis

J. Martinson, J. Kant, P. Randhawa, 2008, Journal of Virology.

Absence of t(14;18) Major and Minor Breakpoints and of BcI-2 Protein

John Calvin Reed, D. Louie, J. Brooks, 2007 .

A unique 7p/12q chromosomal abnormality associated with recurrent abortion and hypofibrinogenemia.

J. Kant, C. Kitchens, A. Cruz, 1987, Blood.

Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis

J. Neoptolemos, D. Whitcomb, R. Pfützer, 2002, Gut.

Global gene profiling and comprehensive bioinformatics analysis of a 46,XY female with pericentric inversion of the Y chromosome

Toshifumi Yokoyama, Yoshiki Matsumoto, Nobuhiko Hoshi, 2010, Congenital anomalies.

Biologic and therapeutic significance of MYB expression in human melanoma.

M. Herlyn, M. Herlyn, G. Zon, 1994, Proceedings of the National Academy of Sciences of the United States of America.

MUM1/IRF4 expression in the circulating compartment of chronic lymphocytic leukemia

S. Swerdlow, F. Craig, M. Melan, 2008, Leukemia & lymphoma.

Immunophenotypic and Genotypic Markers of Follicular Center Cell Neoplasia in Diffuse Large B-Cell Lymphomas

S. Swerdlow, B. Falini, J. Locker, 2000, Modern Pathology.

Identification of ATP citrate lyase as a positive regulator of glycolytic function in glioblastomas

I. Pollack, W. Fellows-Mayle, B. Day, 2009, International journal of cancer.

Goals and objectives for molecular pathology education in residency programs. The Association for Molecular Pathology Training and Education Committee.

T. Greiner, L. Fink, T. Frank, 1999, The Journal of molecular diagnostics : JMD.

Evolution and structure of the fibrinogen genes. Random insertion of introns or selective loss?

J. Malley, G. Crabtree, A. Fornace, 1985, Journal of molecular biology.

Promoter region of interleukin-2 gene undergoes chromatin structure changes and confers inducibility on chloramphenicol acetyltransferase gene during activation of T cells

G. Crabtree, N. Holbrook, J. Kant, 1986, Molecular and cellular biology.

Limitations of the criteria used to diagnose histologic endometritis in epidemiologic pelvic inflammatory disease research.

R. Sweet, J. Kant, M. Chivukula, 2011, Pathology, research and practice.

The pathologic and clinical heterogeneity of lymphocyte-depleted Hodgkin's disease.

E. Jaffe, D. Longo, V. Devita, 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

DNA restriction enzymes and RFLPs in medicine.

J. Kant, 1992, Methods of biochemical analysis.

Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion.

G. Crabtree, M. Simon, A. Fornace, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Organization of the rat γ-fibrinogen gene: Alternative mRNA splice patterns produce the γA and γB (γ′) chains of fibrinogen

G. Crabtree, J. Kant, 1982, Cell.

In situ hybridization for Epstein-Barr virus NotI repeats in posttransplant lymphoproliferative disorder.

J. Kant, J. Tomaszewski, K. Montone, 1992, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Regression and inhibition of sarcoma growth by interference with a radiosensitive T-cell population

J. Kant, K. Hellström, I. Hellström, 1978, The Journal of experimental medicine.

10th Annual Meeting – Association for Molecular Pathology

J. Kant, 2005, Expert review of molecular diagnostics.

Paternal transmission of congenital myotonic dystrophy.

E. Zackai, K. Fischbeck, D. McDonald-McGinn, 1994, Journal of medical genetics.

Human Merkel cell polyomavirus infection I. MCV T antigen expression in Merkel cell carcinoma, lymphoid tissues and lymphoid tumors

S. Swerdlow, J. Kirkwood, M. Mansukhani, 2009, International journal of cancer.

Charcot-Marie-Tooth Disease

J. Kant, Zhiqiang Wang, 2011 .

Comparative biochemical and genetic characterization of clonally related human B-cell lines secreting pathogenic anti-Pr2 cold agglutinins.

J. Kant, S. Spitalnik, L. Silberstein, 1988, Archives of biochemistry and biophysics.

The business of genomic testing: a survey of early adopters

J. M. Crawford, J. Crawford, L. Bry, 2014, Genetics in Medicine.

Down regulation of IL 2 mRNA by antibody to the 50-kd protein associated with E receptors on human T lymphocyte.

J. Kant, M. Kamoun, W. Tadmori, 1986, Journal of immunology.

VP‐1 quasispecies in human infection with polyomavirus BK

J. Kant, P. Randhawa, H. Hirsch, 2012, Journal of medical virology.

Molecular diagnostics on microfabricated electrophoretic devices: from slab gel- to capillary- to microchip-based assays for T- and B-cell lymphoproliferative disorders.

J P Landers, J. Landers, K. Snow, 1999, Clinical chemistry.

Neuronal control of myogenic regulatory factor accumulation in fetal muscle

J. Kant, C. Washabaugh, M. Ontell, 2007, Developmental dynamics : an official publication of the American Association of Anatomists.

Creatine kinase transcript accumulation: Effect of nerve during muscle development

J. Kant, C. Washabaugh, M. Ontell, 1999, Developmental dynamics : an official publication of the American Association of Anatomists.

Immunoglobulin Heavy Chain (IgH) Gene Somatic Hypermutation Status Using Homoduplex-Separated RT-PCR Products.

K. Foon, M. Melan, J. Kant, 2004 .

Hepatosplenic gammadelta T-cell lymphoma: ultrastructural, immunophenotypic, and functional evidence for cytotoxic T lymphocyte differentiation.

P. Nowell, R. DiPaola, D. Wilson, 1997, Human pathology.

Primary low-grade T-helper cell testicular lymphoma.

J. Kant, K. E. Salhany, M. Froberg, 1997, Archives of pathology & laboratory medicine.

Single-copy inverted repeats associated with regional genetic duplications in gamma fibrinogen and immunoglobulin genes.

G. Crabtree, A. Fornace, D. Cummings, 1984, Science.

Genetic testing in chronic pancreatitis

J. Tazelaar, J. Kant, 2003, Expert review of molecular diagnostics.

Seminoma in a postmenopausal woman with a Y;15 translocation in peripheral blood lymphocytes and a t(Y;15)/45,X Turner mosaic pattern in skin fibroblasts.

T. Fujino, K. Fujieda, K. Nagashima, 1998, Journal of medical genetics.

Automated Reticulocyte Counting by Image Analysisand Flow Cytometry

G. Cembrowski, J. Kant, M. Prystowsky, 1989 .

Design and analytical validation of clinical DNA sequencing assays.

Whitney Wooderchak-Donahue, Pinar Bayrak-Toydemir, Elaine Lyon, 2012, Archives of pathology & laboratory medicine.

Carrier Screening for Cystic Fibrosis

John C. Hershey, Mark V. Pauly, Michael T. Mennuti, 1998, Medical decision making : an international journal of the Society for Medical Decision Making.

Structure of the human gamma-fibrinogen gene. Alternate mRNA splicing near the 3' end of the gene produces gamma A and gamma B forms of gamma-fibrinogen.

G. Crabtree, A. Fornace, D. Cummings, 1984, The Journal of biological chemistry.

Two-temperature PCR and heteroduplex detection: application to rapid cystic fibrosis screening.

J. Kant, L. Dodson, 1991, Molecular and cellular probes.

DNA typing of the human MN and Ss blood group antigens in amniotic fluid and following massive transfusion.

J. Eshleman, J. Kant, S. Spitalnik, 1995, American journal of clinical pathology.

Molecular diagnosis of cystic fibrosis.

J. Kant, R. Mcglennen, T. Mifflin, 1995, Clinics in laboratory medicine.

Partial mRNA sequences for human A alpha, B beta, and gamma fibrinogen chains: evolutionary and functional implications.

G. Crabtree, S. Lord, J. Kant, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Genetic counseling for nonsyndromic pancreatitis.

D. Whitcomb, J. Kant, Erin N Fink, 2007, Gastroenterology clinics of North America.

Genetic testing. Counseling, laboratory, and regulatory issues and the EUROPAC protocol for ethical research in multicenter studies of inherited pancreatic diseases.

D. Whitcomb, J. Kant, I. Ellis, 2000, The Medical clinics of North America.

Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening.

J. Ellison, J. Vockley, B. Powell, 2010, Molecular genetics and metabolism.

Interleukin-1 costimulatory activity on the interleukin-2 promoter via AP-1.

M. Karin, K. Muegge, H. Young, 1989, Science.

Reproducibility of synovial fluid analyses. A study among four laboratories.

H. Schumacher, J. Kant, B. Mochan, 1986, Arthritis and rheumatism.

Rapid Communication Absenceoft(14;18) Major andMinor Breakpoints andofBcI-2 Protein Overproduction inReed-Sternberg Cells ofHodgkin's Disease

J. Kant, 1991 .

Diagnosis of posttransplantation lymphoproliferative disorder by endomyocardial biopsy in a cardiac allograft recipient.

J. Kant, J. Tomaszewski, H. Eisen, 1994, The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation.

Advantages of firefly luciferase as a reporter gene: application to the interleukin-2 gene promoter.

L. Kricka, J. Kant, J. Burlein, 1989, Analytical biochemistry.

Genetic testing in acute and chronic pancreatitis

J. Kant, R. Rolston, 2001, Current gastroenterology reports.

MUM1/IRF4 expression in the circulating compartment of chronic lymphocytic leukemia

S. Swerdlow, F. Craig, M. Melan, 2008, Leukemia & lymphoma.

VP‐1 quasispecies in human infection with polyomavirus BK

J. Kant, P. Randhawa, H. Hirsch, 2012, Journal of medical virology.