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Namibian spitting cobra, Naja nigricincta nigricincta : Oral flora and antibiotic sensitivity, a cross-sectional study

SAMJ: South African Medical Journal, 2023-07, Vol.113 (7), p.1256-1262

2023

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Namibian spitting cobra, Naja nigricincta nigricincta (Zebra snake): Antibiotic profile of bacteria cultured from the oral pharynx, venom and snakebite wounds

South African medical journal, 2023-07, Vol.113 (7), p.22-28

2023

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Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer

Gut, 2006-12, Vol.55 (12), p.1781-1788

2006

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In Vitro Fertilization with Preimplantation Genetic Screening

The New England journal of medicine, 2007-07, Vol.357 (1), p.9-17

2007

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Predictive value of thymidylate synthase and dihydropyrimidine dehydrogenase protein expression on survival in adjuvantly treated stage III colon cancer patients

Annals of oncology, 2005-10, Vol.16 (10), p.1646-1653

2005

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Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations

American journal of human genetics, 1999-11, Vol.65 (5), p.1291-1298

1999

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A Human Model for Multigenic Inheritance: Phenotypic Expression in Hirschsprung Disease Requires Both the RET Gene and a New 9q31 Locus

Proceedings of the National Academy of Sciences - PNAS, 2000-01, Vol.97 (1), p.268-273

2000

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Equipping Nurse Practitioner Students With Social Determinants of Health Competencies

The Journal of nursing education, 2024-06, p.1-4

2024

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A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

Nature (London), 1994-01, Vol.367 (6461), p.375-376

1994

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Namibian spitting cobra, Naja nigricincta nigricincta

South African medical journal, 2023-07, Vol.113 (7), p.1256

2023

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A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

Nature genetics, 1996-04, Vol.12 (4), p.445-447

1996

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Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

Human molecular genetics, 1995-05, Vol.4 (5), p.821-830

1995

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Molecular and Clinical Characteristics of MSH6 Variants: An Analysis of 25 Index Carriers of a Germline Variant

American journal of human genetics, 2002-01, Vol.70 (1), p.26-37

2002

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Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy

American journal of human genetics, 1995-10, Vol.57 (4), p.805-808

1995

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A Loss-of-Function Mutation in the Endothelin-Converting Enzyme 1 (ECE-1) Associated with Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction

American journal of human genetics, 1999, Vol.64 (1), p.304-307

1999

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Oncological implications of RET gene mutations in Hirschsprung’s disease

Gut, 1998-10, Vol.43 (4), p.542-547

1998

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PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy

The Lancet (British edition), 1995-04, Vol.345 (8955), p.985-986

1995

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DNA Mismatch Repair Gene Mutations in 55 Kindreds with Verified Or Putative Hereditary Non-Polyposis Colorectal Cancer

Human molecular genetics, 1996-06, Vol.5 (6), p.763-769

1996

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MUTYH and the mismatch repair system : partners in crime?

Human genetics, 2006-03, Vol.119 (1-2), p.206-211

2006

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Spitting cobra (Naja nigricincta nigricincta) bites complicated by rhabdomyolysis, possible intravascular haemolysis, and coagulopathy

SAMJ: South African Medical Journal, 2019-10, Vol.109 (10), p.736-740

2019

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Prognostic significance of K- ras and TP53 mutations in the role of adjuvant chemotherapy on survival in patients with dukes C colon cancer

Diseases of the colon & rectum, 2001-03, Vol.44 (3), p.358-363

2001

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Cytogenetic analysis of epithelial renal‐cell tumors: Relationship with a new histopathological classification

International journal of cancer, 1993-09, Vol.55 (2), p.223-227

1993

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Isolation of the Human Semaphorin III/F Gene (SEMA3F) at Chromosome 3p21, a Region Deleted in Lung Cancer

Genomics (San Diego, Calif.), 1996-02, Vol.32 (1), p.39-48

1996

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The epithelial glycoprotein 2 (EGP-2) promoter-driven epithelial-specific expression of EGP-2 in transgenic mice : A new model to study carcinoma-directed immunotherapy

Cancer research (Chicago, Ill.), 2001-05, Vol.61 (10), p.4105-4111

2001

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P53 mutations in human lung tumors

Cancer research (Baltimore), 1992-04, Vol.52 (7), p.1695-1698

1992

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Namibian spitting cobra, Naja nigricincta nigricincta : Oral flora and antibiotic sensitivity, a cross-sectional study

Namibian spitting cobra, Naja nigricincta nigricincta (Zebra snake): Antibiotic profile of bacteria cultured from the oral pharynx, venom and snakebite wounds

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer

In Vitro Fertilization with Preimplantation Genetic Screening

Predictive value of thymidylate synthase and dihydropyrimidine dehydrogenase protein expression on survival in adjuvantly treated stage III colon cancer patients

Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations

A Human Model for Multigenic Inheritance: Phenotypic Expression in Hirschsprung Disease Requires Both the RET Gene and a New 9q31 Locus

Equipping Nurse Practitioner Students With Social Determinants of Health Competencies

A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

Namibian spitting cobra, Naja nigricincta nigricincta

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

Molecular and Clinical Characteristics of MSH6 Variants: An Analysis of 25 Index Carriers of a Germline Variant

Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy

A Loss-of-Function Mutation in the Endothelin-Converting Enzyme 1 (ECE-1) Associated with Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction

Oncological implications of RET gene mutations in Hirschsprung’s disease

PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy

DNA Mismatch Repair Gene Mutations in 55 Kindreds with Verified Or Putative Hereditary Non-Polyposis Colorectal Cancer

MUTYH and the mismatch repair system : partners in crime?

Spitting cobra (Naja nigricincta nigricincta) bites complicated by rhabdomyolysis, possible intravascular haemolysis, and coagulopathy

Prognostic significance of K- ras and TP53 mutations in the role of adjuvant chemotherapy on survival in patients with dukes C colon cancer

Cytogenetic analysis of epithelial renal‐cell tumors: Relationship with a new histopathological classification

Isolation of the Human Semaphorin III/F Gene (SEMA3F) at Chromosome 3p21, a Region Deleted in Lung Cancer

The epithelial glycoprotein 2 (EGP-2) promoter-driven epithelial-specific expression of EGP-2 in transgenic mice : A new model to study carcinoma-directed immunotherapy

P53 mutations in human lung tumors

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