• <em>KIT</em> Gene Mutation Causing Piebaldism Associated with Multiple Café Au-Lait Like Macules and Freckling: Delineating a Cause of this Coexistence
• <em>MYO5A</em> Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1
• <em>Naa12</em> compensates for <em>Naa10</em> in mice in the amino-terminal acetylation pathway
• A de novo germline mutation of KIT in a white-spotted Brown Swiss cow
• A Familial 4q12 Deletion Involving KIT Gene Causes Piebaldism
• A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families
• A genome-wide association study of deafness in three canine breeds
• A novel c.2326G&gt;A KIT pathogenic variant in piebaldism
• A novel c.2326G>A KIT pathogenic variant in piebaldism
• A novel KIT mutation in a family with expanded syndrome of piebaldism
• A role for the rare endogenous retrovirus β4 in development of Japanese fancy mice
• Acute cerebellar ataxia in Griscelli syndrome type 2
• An allelic series at the <em>EDNRB2</em> locus controls diverse piebalding patterns in the domestic pigeon
• An allelic series at the EDNRB2 locus controls diverse piebalding patterns in the domestic pigeon
• Anakinra as an agent to control hemophagocytic lymphohistiocytosis in Griscelli type 2
• Are dogs with congenital hearing and/or vision impairments so different from sensory normal dogs? A survey of demographics, morphology, health, behaviour, communication, and activities
• Assessing the Activation of Tyrosine Kinase KIT through Free Energy Calculations
• Assessment of Non-cultured Autologous Epidermal Cell Grafting Resuspended in Hyaluronic Acid for Repigmenting Vitiligo and Piebaldism Lesions: A Randomized Clinical Trial
• Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss
• Case series of three adult patients with exceptional clinical presentations of haemophagocytic lymphohistiocytosis
• Comparative outcomes of autologous cultured melanocytes transplantation and non-cultured epidermal cell suspension transplantation in piebaldism patients: A retrospective study
• Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism
• Considering immunologic and genetic evaluation for HLH in neuroinflammation: A case of Griscelli syndrome type 2 with neurological symptoms and a lack of albinism
• Cutaneous granulomas as the presenting manifestation of Griscelli syndrome type 2
• Deafness associated with pigmentation phenotypes in North American yaks (Bos grunniens)
• Delayed diagnosis of Griscelli syndrome type 2 with compound heterozygote <em>RAB27A</em> variants presenting with pulmonary failure
• Development, characterization, and hematopoietic differentiation of Griscelli syndrome type 2 induced pluripotent stem cells
• Diagnostic and therapeutic caveats in Griscelli syndrome
• Does SNAI2 mutation cause human piebaldism and Waardenburg syndrome?
• Donor to recipient ratios in the surgical treatment of vitiligo and piebaldism: a systematic review
• Evaluating possible maternal effect lethality and genetic background effects in <em>Naa10</em> knockout mice
• Evaluating possible maternal effect lethality and genetic background effects in Naa10 knockout mice
• Evaluating possible maternal effect lethality of <em>Naa10</em> knockout mice, and modulation of phenotypes for embryonic and neonatal lethality by genetic background and environment
• Evaluating possible maternal effect lethality of Naa10 knockout mice, and modulation of phenotypes for embryonic and neonatal lethality by genetic background and environment
• Exploiting within-breed variability in the autochthonous Reggiana breed identified several candidate genes affecting pigmentation-related traits, stature and udder defects in cattle
• Fifteen Shades of Grey: Combined Analysis of Genome-Wide SNP Data in Steppe and Mediterranean Grey Cattle Sheds New Light on the Molecular Basis of Coat Color
• First record of atypical pigmentation pattern in fin whale Balaenoptera physalus in the Atlantic Ocean
• First record of partial albinism in the critically endangered Angelshark (Squatina squatina) (Linnaeus, 1758)
• First record of pigmentation disorder in the Fringe-lipped Bat <em>Trachops cirrhosus</em> (Spix, 1823) (Chiroptera: Phyllostomidae) from southeast Brazil
• Functional Analysis of <em>KIT</em> Gene Structural Mutations Causing the Porcine Dominant White Phenotype Using Genome Edited Mouse Models
• Genetic analysis in three Egyptian patients with Griscelli syndrome Type 1 reveals new nonsense mutations in MYO5A
• Genetic and Phenotypic Characteristics of Belted Pig Breeds: A Review
• Glial Cell-Derived Neurotrophic Factor Induces Enteric Neurogenesis and Improves Colon Structure and Function in Mouse Models of Hirschsprung Disease
• Griscelli syndrome type 1: a novel pathogenic variant, and review of literature
• Griscelli Syndrome Type 1: Hair Microscopy Clinches the Diagnosis
• Griscelli Syndrome Type 2 Presenting with Isolated Neurologic Disorder
• Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector Engagement
• Griscelli syndrome type 3 in Ethiopian sisters resulting from a homozygous missense mutation in MLPH
• Hair pigment distribution changes after haematopoietic stem cell transplantation in Griscelli syndrome type 2
• Hematopoietic stem cell transplantation in children with Griscelli syndrome type 2: a single-center report on 35 patients
• Hemophagocytic Lymphohistiocytosis in Patients With Primary Immunodeficiency
• Identification of <em>kit-ligand a</em> as the Gene Responsible for the Medaka Pigment Cell Mutant <em>few melanophore</em>
• Impact of breeding for coat and spotting patterns on the population structure and genetic diversity of an islander endangered dog breed
• Impact of graft cell density and viability on repigmentation upon noncultured autologous cell suspension transplantation in vitiligo and piebaldism
• Irregular spots on body surfaces of vertebrates induced by supercritical pitchfork bifurcations
• KIT Gene Mutation Causing Piebaldism Associated with Multiple Cafe Au-Lait Like Macules and Freckling: Delineating a Cause of this Coexistence
• KIT Mutation Associated with Depigmented Patches Regression and Multiple Cafe-au-lait Macules Development in a Patient with Piebaldism: A Case Report
• KIT-related piebaldism in a Chinese girl
• Lesional CD8+ T Cell Number Predicts Surgical Outcomes of Melanocyte-Keratinocyte Transplantation Surgery for Vitiligo
• Lesional CD8+ T-Cell Number Predicts Surgical Outcomes of Melanocyte-Keratinocyte Transplantation Surgery for Vitiligo
• Localized, time-dependent responses of rat cranial bone to repeated mild traumatic brain injuries
• Long-term observation of a piebald patient showing pigmentation within leukoderma
• Meek micrografting, a novel surgical technique for the treatment of vitiligo and piebaldism: A case series
• Melanocyte lineage cells in piebald skin
• Methylome and transcriptome analyses of three different degrees of albinism in apple seedlings
• MULTIPLE CAFÉ-AU-LAIT MACULES AND INTERTRIGINOUS FRECKLING: BEYOND THE RASOPATHIES
• Necrotizing pneumonia and purulent meningitis caused by bloodstream infection of CA-MRSA in a child: A rare case report
• Neonatal Onset of Hemophagocytic Lymphohistiocytosis Due to Prenatal Varicella-Zoster Infection in a Neonate with Griscelli Syndrome Type 2
• Novel Germline KIT Variants in Families With Severe Piebaldism: Case Series and Literature Review
• Novel homozygous nonsense variant in MLPH causing Griscelli syndrome type 3 in a consanguineous Pakistani family
• Novel pathogenic variants in <em>KIT</em> gene in three Chinese piebaldism patients
• Novel pathogenic variants in KIT gene in three Chinese piebaldism patients
• Novel retinal finding in a patient with 4q12 deletion
• Observations of hypomelanosis in the nurse shark Ginglymostoma cirratum
• Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation
• On the role of TFEC in reptilian coloration
• Partial albinism and immunodeficiency in patients with Hermansky-Pudlak Type II: Introducing 2 novel mutations
• PET morphology helps distinguish solitary and solid pulmonary tuberculosis from non-small cell lung cancer
• Piebaldism
• Piebaldism
• Piebaldism and chromatophore development in reptiles are linked to the tfec gene
• Piebaldism Associated with Cafe-au-lait Macules and Intertriginous Freckling: A Case Report and Review of the Literature
• Piebaldism resulting from a novel deletion mutation of KIT gene in a five-generation Chinese family
• Piebaldism with cafe-au-lait macules resulting from a novel mutation of KIT gene in a three-generation Chinese family
• Recipient-to-Donor Ratios in the Surgical Treatment of Vitiligo, Leukoderma, and Piebaldism: A Retrospective Review
• Repigmentation of White Forelock in a Familial Case of Piebaldism Reported via Teledermatology in the COVID-19 Era
• Report of two Japanese patients with piebaldism including a novel mutation in KIT
• Retraction: Piebaldism: A Brief Report and Review of the Literature
• Reverse Genetic Approach to Identify Regulators of Pigmentation using Zebrafish
• Secondary Degeneration Impairs Myelin Ultrastructural Development in Adulthood following Adolescent Neurotrauma in the Rat Optic Nerve
• Striking contiguous depigmentation across the lower limbs in piebaldism, its implications for understanding melanocytic migration, development
• STRING data mining of GWAS data in canine hereditary pigment-associated deafness
• Successful haploidentical bone marrow transplantation in Griscelli syndrome type 2 with non-busulfan-based regimen and post-transplantation cyclophosphamide: a case report and review of the literature
• Successful rescue of a lethal Griscelli syndrome type 2 presenting with neurological involvement and hemophagocytic lymphohistiocytosis: a case report
• The First Korean Case of Griscelli Syndrome Type 2 With Hemophagocytic Lymphohistiocytosis and Partial Albinism
• The investigation on allelic, genotypic frequencies and gene expression study in coding region of tyrosinase gene in Deoni cattle breed of western India
• The Shan people's health beliefs, knowledge and perceptions of dengue in Eastern Shan Special Region IV, Myanmar
• Tracing the retina to analyze the integrity and phagocytic capacity of the retinal pigment epithelium
• Transcriptome analysis provides insights into copper toxicology in piebald naked carp (Gymnocypris eckloni)
• Waardenburg's Syndrome Type IIA with Partial Albinism