プロフィール詳細

プロジェクトを作成

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☆☆☆☆☆

Dr. Herlina H.に依頼

Australia

Freelance, contract-to-hire, molecular geneticist | Expert in molecular biology techniques at the wet laboratory.

プロフィール概要

30+ years experience in the laboratory work using various molecular biology techniques including, but not limited to, cloning, PCR, sequencing, array, blotting on DNA, RNA and protein. I have also done mouse work, histology, and biochemical techniques. I am able to pick up new techniques quickly and adjust to new laboratories easily, saving you from training new employees to do a few months of work.

専門分野

• ★ Molecular Biology
• ☆ Drug Development
• ☆ Cancer Research

サービス

• Writing
• Research

Writing Newswriting

Research Fact Checking, Gray Literature Search, Systematic Literature Review, Secondary Data Collection

職務経験

Freelance Scientist

Scientist4Hire

11月 2019 - 現在

Senior Reserach Officer

QIMR Berghofer Medical Research Institute

8月 2006 - 現在

Queensland Centre for Mental Health Research

2001 - 7月 2006

学歴

PhD

University of Minnesota Twin Cities

- 1995

MSc

University of Minnesota Twin Cities

- 1990

BSc (Biologi)

Universitas Indonesia Fakultas Matematika dan Ilmu Pengetahuan Alam

- 1985

認定資格

• 認定資格の詳細は未入力です。

出版物

JOURNAL ARTICLE

(2020). Murine dorsal hair type is genetically determined by polymorphisms in candidate genes that influence BMP and WNT signalling . Experimental Dermatology.

(2019). Unexpected High Levels of BRN2/POU3F2 Expression in Human Dermal Melanocytic Nevi . Journal of Investigative Dermatology.

(2019). Different genetic mechanisms mediate spontaneous versus UVR-induced malignant melanoma . eLife.

(2017). Keratinocyte Sonic Hedgehog upregulation drives the development of giant congenital nevi via paracrine Endothelin-1 secretion. J Invest Dermatol.

(2017). Melanocyte transformation requires complete loss of all pocket protein function via a mechanism that mitigates the need for MAPK pathway activation . Oncogene.

(2016). A mutation in the Cdon gene potentiates congenital nevus development mediated by NRAS(Q61K). Pigment Cell Melanoma Research.

(2015). Murine melanomas accelerated by a single UVR exposure carry photoproduct footprints but lack UV signature C>T mutations in critical genes . Oncogene.

(2015). Melanoma susceptibility as a complex trait . Oncogene.

(2015). Lack of evidence from a transgenic mouse model that the activation and migration of melanocytes to the epidermis after neonatal UVR enhances melanoma development . Journal of Investigative Dermatology.

(2015). Hair follicle melanocyte precursors are awoken by ultraviolet radiation via a cell extrinsic mechanism . Photochemical & Photobiological Sciences.

(2014). Differential effects of ultraviolet irradiation in neonatal versus adult mice are not explained by defective macrophage or neutrophil infiltration . Journal of Investigative Dermatology.

(2013). UVB-induced melanocyte proliferation in neonatal mice driven by CCR2-independent recruitment of Ly6clowMHCIIhi macrophages . Journal of Investigative Dermatology.

(2013). Plasticity of melanoma in vivo . Pigment Cell & Melanoma Research.

(2012). Modeling epidermal melanoma in mice . Journal of Investigative Dermatology.

(2011). Superficial spereading-like melanomas in Arf-/-::Tyr-NrasQ61K::K14-Kitl mice . Journal of Investigative Dermatology.

(2010). Differential roles of the pRb and Arf/p53 pathways in murine naevus and melanoma genesis . Pigment Cell & Melanoma Reserach.

(2010). No association between neuregulin 1 and psychotic symptoms in Alzheimer's disease patients . Journal of Alzheimer Disease.

(2008). Association of PIP5K2A with schizophrenia . American Journal of Medical Genetics B Neuropsychiatric Genetics.

(2008). Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression . Psychiatric Genetics.

(2008). Association study of candidate variants of COMT with neuroticism, anxiety and depression . American Journal of Medical Genetics B Neuropsychiatric Genetics.

(2008). Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21 . American Journal of Medical Genetcis B Neurpsychiatric Genetics.

(2008). Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays . Cancer Research.

(2007). SiDCoN. PLoS One.

(2006). Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. Twin Research and Human Genetics.

(2006). Polymorphisms in the vitamin D receptor and their associations with risk of schizophrenia and selected anthropometric measures. American Journal of Human Biology.

(2006). Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia. Molecular Psychiatry.

(2006). Polimorfisme Adenine Nucleotide Translocator-2 pada populasi individu normal dan Leber's Hereditary Optic Neuropathy. Jurnal Kedokteran Brawijaya.

(2005). Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. Molecular Psychiatry.

(2003). Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific region. American Journal of Medical Genetics B Neuropsychiatric Genetics.

(2001). Length variations in the COII-tRNA(Lys) intergenic region of mitochondria DNA in Indonesian populations. Human Biology.

(1998). Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy. Journal of Medical Genetics.

(1991). Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinism. Journal of Investigative Dermatology.

(1991). PCR detection of a TaqI polymorphism in the CCAATT box of the human tyrosinase (TYR) gene. Nucleic Acids Research.

BOOK CHAPTER

(2015). Mouse models for actinic keratosis and squamouse cell carcinoma. Current Problems in Dermatology.