P. Henthorn

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Marking of peripheral T-lymphocytes by retroviral transduction and transplantation of CD34+ cells in a canine X-linked severe combined immunodeficiency model.

S. Suter, T. A. Gouthro, T. O'Malley, 2007, Veterinary immunology and immunopathology.

Optimized Transduction of Canine Paediatric CD34+ Cells Using an MSCV-based Bicistronic Vector

S. Suter, T. A. Gouthro, P. Mcsweeney, 2006, Veterinary Research Communications.

Severe Papillomavirus Infection Progressing to Metastatic Squamous Cell Carcinoma in Bone Marrow-Transplanted X-Linked SCID Dogs

K. Weinberg, B. Hartnett, P. Moore, 2006, Journal of Virology.

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

Carolyn J. Brown, H. Willard, C. Brown, 1993, Human molecular genetics.

Dilated Cardiomyopathy in Juvenile Portuguese Water Dogs

P. Henthorn, D. Dambach, M. Sleeper, 2002, Journal of veterinary internal medicine.

Identification of a retrovirus-like repetitive element in human DNA.

D. Mager, P. Henthorn, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Heritability and complex segregation analysis of naturally-occurring diabetes in Australian Terrier Dogs

P. Henthorn, T. Famula, Mei Lun Mui, 2020, PloS one.

The keeshond defect in cardiac conotruncal development is oligogenic1

E. Kirkness, R. Spielman, E. Ostrander, 2005, Human Genetics.

Hypophosphatasia: levels of bone alkaline phosphatase immunoreactivity in serum reflect disease severity.

Denise, P. Henthorn, M. Whyte, 1996, The Journal of clinical endocrinology and metabolism.

Assignment of 10 canine genes to the canine linkage and comparative maps.

E. Kirkness, E. Ostrander, P. Henthorn, 2004, Animal genetics.

Evaluation of the dynactin 1 gene in Leonbergers and Labrador Retrievers with laryngeal paralysis.

P. Henthorn, D. Holt, D. C. Brown, 2016, American journal of veterinary research.

The entire beta-globin gene cluster is deleted in a form of gamma delta beta-thalassemia

S. Orkin, S. Antonarakis, F. Grosveld, 1983 .

Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia.

M. Podgornik, P. Henthorn, S. Mumm, 2002, Molecular genetics and metabolism.

Hereditary β-mannosidosis in a dog: Clinicopathological and molecular genetic characterization.

U. Giger, P. Henthorn, Ping Wang, 2019, Molecular genetics and metabolism.

Molecular Basis of Canine Muscle Type Phosphofructokinase Deficiency*

U. Giger, H. Stedman, P. Henthorn, 1996, The Journal of Biological Chemistry.

Expression of a human placental alkaline phosphatase gene in transfected cells: use as a reporter for studies of gene expression.

H. Harris, T. Kadesch, P. Zervos, 1988, Proceedings of the National Academy of Sciences of the United States of America.

SLC3A1 and SLC7A9 mutations in autosomal recessive or dominant canine cystinuria: a new classification system.

Jun Liu, U. Giger, A. Sewell, 2013, Journal of veterinary internal medicine.

cDNA cloning of alkaline phosphatase from rat osteosarcoma (ROS 17/2.8) cells

H. Harris, G. Rodan, M. Weiss, 1987, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Coordinate modulation of transfected HSV thymidine kinase and human globin genes

R. Kucherlapati, A. Skoultchi, P. Henthorn, 1983, Cell.

Introduction and expression of a fetal human globin gene in mouse fibroblasts

R. Kucherlapati, A. Skoultchi, P. Henthorn, 1982, Molecular and cellular biology.

Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs

U. Giger, P. Henthorn, M. Casal, 2000, Human Genetics.

Cloning of the canine beta-glucuronidase cDNA, mutation identification in canine MPS VII, and retroviral vector-mediated correction of MPS VII cells.

J. Fyfe, G. Aguirre, M. Haskins, 1998, Genomics.

Canine X-linked severe combined immunodeficiency

B. Hartnett, P. Felsburg, P. Henthorn, 1998, Immunologic research.

Expression and Function of TLR 2 , TLR 4 , and Nod 2 in Primary Canine Colonic Epithelial Cells

P. Moore, P. Felsburg, P. Henthorn, 2008 .

Expression and function of TLR2, TLR4, and Nod2 in primary canine colonic epithelial cells.

P. Moore, P. Felsburg, P. Henthorn, 2006, Veterinary immunology and immunopathology.

T cell repertoire development in XSCID dogs following nonconditioned allogeneic bone marrow transplantation.

K. Weinberg, B. Hartnett, P. Moore, 2007, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Structure of the human liver/bone/kidney alkaline phosphatase gene.

H. Harris, M. Weiss, T. Kadesch, 1988, The Journal of biological chemistry.

Mild autosomal dominant hypophosphatasia: in utero presentation in two families.

C. Moore, C. Curry, D. Weaver, 1999, American journal of medical genetics.

A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.

D. Mager, P. Henthorn, O. Smithies, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Comparative mapping of the DiGeorge region in the dog and exclusion of linkage to inherited canine conotruncal heart defects.

M. Budarf, P. Henthorn, D. Patterson, 1999, The Journal of heredity.

Ex vivo γ-retroviral gene therapy of dogs with X-linked severe combined immunodeficiency and the development of a thymic T cell lymphoma.

L. Burkly, T. O'Malley, B. Hartnett, 2011, Veterinary immunology and immunopathology.

Effect of ex vivo culture of CD34+ bone marrow cells on immune reconstitution of XSCID dogs following allogeneic bone marrow transplantation.

P. Moore, P. Felsburg, P. Henthorn, 2009, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Thymopoiesis and T cell development in common gamma chain-deficient dogs

T. A. Gouthro, B. Hartnett, P. Felsburg, 2003, Immunologic research.

Drug selection with paclitaxel restores expression of linked IL-2 receptor γ-chain and multidrug resistance (MDR1) transgenes in canine bone marrow

M. Gottesman, J. Puck, D. Bodine, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q

E. Kirkness, A. Schäffer, J. Fyfe, 2003, Mammalian Genome.

Isolation and characterization of pediatric canine bone marrow CD34+ cells.

S. Suter, T. A. Gouthro, P. Mcsweeney, 2004, Veterinary immunology and immunopathology.

Epidermolysis bullosa simplex in sibling Eurasier dogs is caused by a PLEC non‐sense variant

P. Henthorn, T. Olivry, Ping Wang, 2017, Veterinary dermatology.

Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin

James T. Elder, M. Groudine, D. Mager, 1990, Molecular and cellular biology.

Sequence and characterization of the human intestinal alkaline phosphatase gene.

H. Harris, T. Kadesch, P. Henthorn, 1988, The Journal of biological chemistry.

Human placental and intestinal alkaline phosphatase genes map to 2q34-q37.

H. Harris, B. Emanuel, M. Weiss, 1987, American journal of human genetics.

Nucleotide and amino acid sequences of human intestinal alkaline phosphatase: close homology to placental alkaline phosphatase.

C. Slaughter, H. Harris, P. Henthorn, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Isolation and characterization of a cDNA encoding a human liver/bone/kidney-type alkaline phosphatase.

C. Slaughter, H. Harris, M. Weiss, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Products of two common alleles at the locus for human placental alkaline phosphatase differ by seven amino acids.

C. Slaughter, H. Harris, K. Rothblum, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Missense mutations of the tissue-nonspecific alkaline phosphatase gene in hypophosphatasia.

P. Henthorn, M. Whyte, Michael, 1992, Clinical chemistry.

A Defect in NIPAL4 Is Associated with Autosomal Recessive Congenital Ichthyosis in American Bulldogs

P. Henthorn, Ping Wang, M. Casal, 2017, PloS one.

A Chinese G gamma + (A gamma delta beta)zero thalassemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints.

D. Mager, P. Henthorn, O. Smithies, 1985, Nucleic acids research.

Glomerulopathy and mutations in NPHS1 and KIRREL2 in soft-coated Wheaten Terrier dogs

P. Henthorn, M. Raducha, M. Littman, 2013, Mammalian Genome.

X-linked severe combined immunodeficiency in a family of Cardigan Welsh corgis.

P. Felsburg, P. Henthorn, R. Somberg, 1997, Journal of the American Animal Hospital Association.

Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34.

K. Buetow, H. Harris, B. Emanuel, 1988, Genomics.

Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carriers of hypophosphatasia corrects during pregnancy.

P. Henthorn, S. Coburn, M. Whyte, 1995, The Journal of clinical investigation.

Changing paradigms in diagnosis of inherited defects associated with urolithiasis.

P. Henthorn, D. Bannasch, 2009, The Veterinary clinics of North America. Small animal practice.

UPDATES ON CYSTINURIA AND FANCONI SYNDROME: AMINO ACIDURIAS IN DOGS

U. Giger, A. Sewell, K. Raj, 2015 .

Mutation identification in a canine model of X-linked ectodermal dysplasia

P. Henthorn, M. Casal, P. Werner, 2005, Mammalian Genome.

Aberrant properties of alkaline phosphatase in patient fibroblasts correlate with clinical expressivity in severe forms of hypophosphatasia.

P. Henthorn, M. Whyte, K. Fedde, 1996, The Journal of clinical endocrinology and metabolism.

Hypophosphatasia: levels of bone alkaline phosphatase immunoreactivity in serum reflect disease severity.

P. Henthorn, M. Whyte, C. Hill, 1996, The Journal of clinical endocrinology and metabolism.

Canine X-linked severe combined immunodeficiency.

H. Ochs, B. Hartnett, P. Moore, 1999, Veterinary immunology and immunopathology.

Bone marrow transplantation for canine X-linked severe combined immunodeficiency.

H. Ochs, K. Weinberg, B. Hartnett, 1999, Veterinary immunology and immunopathology.

Full immunologic reconstitution following nonconditioned bone marrow transplantation for canine X-linked severe combined immunodeficiency.

H. Ochs, K. Weinberg, B. Hartnett, 1997, Blood.

A single nucleotide insertion in the canine interleukin-2 receptor gamma chain results in X-linked severe combined immunodeficiency disease.

P. Felsburg, P. Henthorn, M. Casal, 1995, Veterinary immunology and immunopathology.

Familial Glomerulonephropathy in the Bullmastiff

P. Henthorn, D. Dambach, M. Casal, 2004, Veterinary pathology.

MHC class II association study in eight breeds of dog with hypoadrenocorticism

C. Mellersh, W. Ollier, J. Massey, 2013, Immunogenetics.

Inherited neuroaxonal dystrophy in dogs causing lethal, fetal‐onset motor system dysfunction and cerebellar hypoplasia

J. Fyfe, R. Castellani, D. Goldowitz, 2010, The Journal of comparative neurology.

Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia.

P. Henthorn, M. Whyte, M. A. Lafferty, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Infantile hypophosphatasia: Successful prenatal assessment by testing for tissue‐non‐specific alkaline phosphatase isoenzyme gene mutations

P. Henthorn, M. Whyte, 1995, Prenatal diagnosis.

Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpoints.

D. Mager, P. Henthorn, O. Smithies, 1990, Genomics.

Physical and linkage mapping of human chromosome 17 loci to dog chromosomes 9 and 5.

P. Henthorn, D. Patterson, M. Raducha, 1997, Genomics.

The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22.

J. Puck, T. Kadesch, P. Henthorn, 1991, Genomics.

Mechanism of Deletion Removing All Dystrophin Exons in a Canine Model for DMD Implicates Concerted Evolution of X Chromosome Pseudogenes

J. Kornegay, H. Stedman, P. Henthorn, 2016, Molecular therapy. Methods & clinical development.

Two distinct transcription factors that bind the immunoglobulin enhancer microE5/kappa 2 motif.

T. Kadesch, P. Henthorn, M. Kiledjian, 1990, Science.

A novel locus for dilated cardiomyopathy maps to canine chromosome 8.

P. Henthorn, T. V. Van Winkle, M. Sleeper, 2008, Genomics.

Protein tyrosine phosphatase 1B is a key regulator of IFNAR1 endocytosis and a target for antiviral therapies

D. Baker, S. Fuchs, P. Henthorn, 2012, Proceedings of the National Academy of Sciences.

Retroviral marking of canine bone marrow: long-term, high-level expression of human interleukin-2 receptor common gamma chain in canine lymphocytes.

J. Puck, D. Bodine, M. Haskins, 1998, Blood.

Sry-negative XX sex reversal in a family of Norwegian Elkhounds.

U. Giger, P. Henthorn, D. Dambach, 1999, Journal of veterinary internal medicine.

Restriction fragment length polymorphism of the T-cell receptor beta-chain gene in dogs.

P. Henthorn, A. Tipold, R. Somberg, 1996, Veterinary immunology and immunopathology.

Transplantation of X-linked severe combined immunodeficient dogs with CD34+ bone marrow cells.

K. Weinberg, S. Suter, B. Hartnett, 2002, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency.

J. Puck, M. Conley, P. Henthorn, 1997, Blood.

Postnatal development of T cells in dogs with X-linked severe combined immunodeficiency.

B. Hartnett, P. Moore, P. Felsburg, 1996, Journal of immunology.

IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease.

J. Puck, P. Felsburg, P. Henthorn, 1994, Genomics.

Murine liver arylsulfatase B processing influenced by region on chromosome 17

J. Womack, P. Henthorn, W. Daniel, 1981, Biochemical Genetics.

Polymorphisms in canine platelet glycoproteins identify potential platelet antigens.

P. Henthorn, M. Callan, N. Mason, 2013, Comparative medicine.

The entire beta-globin gene cluster is deleted in a form of gamma delta beta-thalassemia.

S. Orkin, S. Antonarakis, F. Grosveld, 1983, Blood.

An Exploratory Association Analysis of the Insulin Gene Region With Diabetes Mellitus in Two Dog Breeds

M. Devoto, Fan Wang, P. Henthorn, 2019, The Journal of heredity.

Anchoring of canine linkage groups with chromosome-specific markers

E. Ostrander, C. Mellersh, G. Acland, 1999, Mammalian Genome.

RXRA and HSPA5 map to the telomeric end of dog chromosome 9.

J. Kehler, P. Henthorn, L. Lyons, 1998, Animal genetics.

Feline adult beta-globin polymorphism reflected in restriction fragment length patterns.

U. Giger, P. Henthorn, T. Asakura, 1999, The Journal of heredity.

A comparative approach to physical and linkage mapping of genes on canine chromosomes using gene-associated simple sequence repeat polymorphisms illustrated by studies of dog chromosome 9.

P. Henthorn, D. Patterson, M. Raducha, 1999, The Journal of heredity.

Putative candidate genes for canine hypoadrenocorticism (Addison's disease) in multiple dog breeds

J. Massey, P. Henthorn, E. Husebye, 2014, Veterinary Record.

Succinate dehydrogenase subunit D and succinate dehydrogenase subunit B mutation analysis in canine phaeochromocytoma and paraganglioma.

P. Henthorn, B. Robinson, D. Holt, 2014, Journal of comparative pathology.

Sequence of the cDNA encoding ITF-2, a positive-acting transcription factor.

T. Kadesch, P. Henthorn, R. McCarrick‐Walmsley, 1990, Nucleic acids research.

A survey of canine expressed sequence tags and a display of their annotations through a flexible web-based interface.

G. Hannon, W. McCombie, T. Zutavern, 2003, The Journal of heredity.

Molecular basis of feline beta-glucuronidase deficiency: an animal model of mucopolysaccharidosis VII.

J. Fyfe, U. Giger, N. Yuhki, 1999, Genomics.

A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats.

J. Fyfe, U. Giger, N. Yuhki, 2007, Molecular genetics and metabolism.

Canine GM2‐Gangliosidosis Sandhoff Disease Associated with a 3‐Base Pair Deletion in the HEXB Gene

P. Henthorn, E. Galban, T. Takedai, 2017, Journal of veterinary internal medicine.

Localization of two alkaline phosphatase genes to the proximal region of mouse chromosome 1.

H. Harris, P. Gros, P. Henthorn, 1989, Cytogenetics and cell genetics.

Identification of the Identical Human Mutation in ACVR1 in 2 Cats With Fibrodysplasia Ossificans Progressiva

P. Henthorn, M. Casal, E. Shore, 2019, Veterinary pathology.

Sequence of the cDNA encoding ITF-1, a positive-acting transcription factor.

T. Kadesch, P. Henthorn, R. McCarrick‐Walmsley, 1990, Nucleic acids research.

Epilepsy in Irish Wolfhounds.

P. Henthorn, M. Casal, Richard M Munuve, 2006, Journal of veterinary internal medicine.

An ABCC9 Missense Variant Is Associated with Sudden Cardiac Death and Dilated Cardiomyopathy in Juvenile Dogs

P. Henthorn, K. Minor, M. Sleeper, 2023, Genes.

MHC class II association study in eight breeds of dog with hypoadrenocorticism

C. Mellersh, W. Ollier, J. Massey, 2013, Immunogenetics.

Familial insulin-dependent diabetes mellitus in Samoyed dogs.

P. Henthorn, S. Kimmel, R. Hess, 2002, Journal of the American Animal Hospital Association.

Evaluation for type 1 diabetes associated autoantibodies in diabetic and non-diabetic Australian terriers and Samoyeds

M. Atkinson, P. Henthorn, C. Wasserfall, 2020, Canine Medicine and Genetics.

Mutation Analysis of IL 2 RG in Human X-Linked Severe Combined Immunodeficiency

J. Puck, M. Conley, P. Henthorn, 1997 .

Congenital peritoneopericardial diaphragmatic hernia in a family of Persian cats

P. Henthorn, M. Casal, Carol Margolis, 2018, JFMS open reports.

Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.

A. Dutra, J. Puck, P. Felsburg, 1994, Genomics.

Genetic counseling in the era of molecular diagnostics.

M. Haskins, P. Henthorn, M. Casal, 2006, Theriogenology.

A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy

R. Agarwala, A. Schäffer, J. Fyfe, 2011, neurogenetics.

Glomerulopathy and mutations in NPHS1 and KIRREL2 in soft-coated Wheaten Terrier dogs

P. Henthorn, M. Raducha, M. Littman, 2013, Mammalian Genome.

Globin gene expression in hereditary persistence of fetal haemoglobin and (delta beta) (0)-thalassaemia.

C. Stoeckert, S. Surrey, M. Poncz, 1988, Oxford surveys on eukaryotic genes.